ANTICANCER COMPOUNDS

Field of the Invention

The present invention relates to compounds for inhibition of uncontrolled cell proliferation, particularly cancer stem cells. The present invention also relates to the compounds for use in the treatment of cancer.

Background of the Invention

Cancer is a condition in which abnormal cells proliferate and spread at any place in the body. In other words, cancer is an uncontrolled growth of abnormal cells. Cancer is a leading cause of death worldwide. It remains the second most dreadful disease in India, killing more than three million patients each year. It is of major concern in India and is reported to be one of the ten leading causes of deaths in India.

While molecularly-targeted therapies are available for treatment of cancer for a high price, majority of the world population rely on standard chemotherapy. The standard anticancer regiment targets most of the dividing cancer cells and not quiescent or slow-dividing cancer stem cells (CSCs). Even though, CSCs have been identified a while ago, scientists around the globe are still looking to find CSC-targeted agents and unfortunately, until today, there is none available in the market to specifically target CSCs.

CSCs and work either alone or in combination with the standard therapies to provide effective treatment option for the cancer patients.

Summary of Invention

The present invention provides compounds for the treatment of cancer, particularly cancer stem cells that show preferential toxicity towards malignant cells, particularly in cancer cell lines such as breast cancer, and/or prostate cancer cell lines.

In one aspect of the present invention, compound of Formula III is provided:

where E and Z is selected from C, O, N, S, salts of N such as N. HCl; Q is O, S, -CH ₂ O-, -NY', wherein Y' is selected from -H, alkyl, SOOCH3; R ⁵ is -H, -CI, when E and/or Z is -C; R ⁶ and R ⁷ each independently is selected from -H, alkoxy, alkyl, substituted or unsubstituted aromatic group, -NF1 ₂ , -N0 ₂ , - NHCOCH ₃ , -CN, -0-, halogen, -OCF ₃ or R ⁶ and R ⁷ together form a heterocyclic ring; R ⁸ is -H, -CI, when E and/or Z is -C; R ₉ is -CH2-0— CH2, -COOH, -X where can be F, CI, Br, alkyl such as -CH ₃ , - OH, alkoxy such as -OMe, NHCOCH ₃ , H, NH ₂ ; ^U and R ¹² each independently is selected from -H, or R ¹¹ and R ¹² can be substituted or unsubstituted 5- or 6-membered ring such as lactone, -C(0)0-alkyl such as -C(0)OC ₂ H5 ; R is selected from

SOO-CH ₃ , -SQOPh, , -CH ₂ C(Q)N(CH ₃ ) ₂ , -C(0)NHPh, -C(0)NHPhOH, - C(S)NHPh, -CH ₂ Ph, -COAr, -SOOAr, -CONHAr, -CH ₂ Ar, -CSNHAr, wherein, R ¹³ is selected from -OH, -NH ₂ , -NHCOCH3, X = F, CI, Br, alkyl, acetyl, C ₃ -C§ acyl group; R ¹⁴ is selected from alkoxy, -OMe, -OH, NH _2, - NHCOCH _3, . X = F, CI, Br, alkyl, acetyl, C ₃ -C ₈ acyl group; R ¹⁵ is selected from alkoxy, -OMe, -OH, -H, Br, NH ₂ , X - F, CI, Br, alkyl, acetyl, C ₃ -C ₃ acyl group; R ¹⁶ is selected from -H, -CH ₂ OH, -OH, alkyl, alkoxy; R ¹⁷ is selected from alkyl. In another aspect of the present invention, compound of Formula IV is provided:

substituted or unsubstituted aromatic group, -NI K -N0 ₂ , -NHCOCH ₃ , -CN, -0-, halogen, -OCF ₃ or R ⁶ and R ⁷ together form a heterocyclic ring; R is selected from:

CH ₃ , -SOOPh, , -CH ₂ C(0)N(CH ₃ ) ₂ , -C(0)NHPh, -C(0)NHPhOH, -C(S)NHPh, -CH ₂ Ph, -COAr, -SOOAr, -CONHAr, -CH ₂ Ar, -CSNHAr; R ¹¹ and R ¹² each independently is selected from -H, or R ¹¹ and R ¹² can be substituted or unsubstituted 5- or 6- membered ring such as lactone, -C(0)0-alkyl such as - C(0)OC ₂ ¾;

In a preferred aspect of the invention, compound of Formula V is provided:

In another preferred aspect, compound of Formula VI is provided:

In another aspect, compound of Formula VII is providec

In another aspect, compound of Formula Vlll is prov

In a further aspect, compound of Formula IX is provided:

In a further aspect a compound of Formula X is provided:

In a further aspect, a compound of Formula II is provided:

In a further aspect, a compound of Formula XIV is provided:

The present invention provides compounds V to XIV for use in treatment of cancer.

In further aspect of the present invention, compounds of Formula V to XIV for use in the treatment of cancer is provided. The cancer can be breast, oral, prostate, brain, blood, bone marrow, liver, pancreas, skin, kidney, colon, ovary, lung, testicle, penis, thyroid, parathyroid, pituitary, thymus, retina, uvea, conjunctiva, spleen, head, neck, trachea, gall bladder, rectum, salivary gland, adrenal gland, throat, esophagus, lymph nodes, sweat glands, sebaceous glands, muscle, heart, or stomach cancer.

In a preferred aspect of the present invention, the compounds of Formula V or VI can be for use in the treatment of breast and/or prostate cancer.

In yet another aspect of the present invention, a pharmaceutical composition having a compound of Formula V to Formula XIV and pharmaceutically acceptable excipient including carrier, adjuvant, vehicle or mixtures thereof is provided. The composition of the present invention can be used in the treatment of cancer. The cancer includes breast, oral, prostate, brain, blood, bone marrow, liver, pancreas, skin, kidney, colon, ovary, lung, testicle, penis, thyroid, parathyroid, pituitary, thymus, retina, uvea, conjunctiva, spleen, head, neck, trachea, gall bladder, rectum, salivary gland, adrenal gland, throat, esophagus, lymph nodes, sweat glands, sebaceous glands, muscle, heart, or stomach cancer. In a preferred aspect, the composition can be used for the treatment of breast and/or prostate cancer.

In a further aspect of the present invention, a method of treating cancer by administering an effective amount of at least one of compounds of present invention is provided. In a preferred aspect, a method of treating cancer including administering an effective amount of compound of formula V or VI is provided. The method of treatment including administering an effective amount of compound of formula V or VI, can be for treating breast cancer and/ or a prostate cancer.

Brief Description of the Drawings

Fig 1. Shows effect of compound of Formula V on cancer cell lines MDAMB231 and PC3 compared to standard chemo therapeutic drug Cisplatin in MTT assay.

Fig 2. Shows effect of compound of Formula V on cancer cell lines MDAMB231 and PC3 compared to standard chemo therapeutic drug Cisplatin in soft Agar Assay. Fig 3 Shows the percentage viability of spheres of MDAMB231 in the presence of compound of Formula V compared to standard chemo therapeutic drug

Fig 4 Shows that there is decrease in percentage viability of spheres of PC3 in presence of Formula V compared to standard chemotherapeutic drug Cisplatin.

Fig 5 Shows the effect of compound of Formula VI on MDAMB231 and PC3 cancer cell lines compared to standard chemo therapeutic drug Cisplatin in MTT assay.

Fig 6 Shows the effect of compound of Formula VI on MDAMB231 and PC3 cancer cell lines compared to standard chemo therapeutic drug Cisplatin in Soft Agar Assay. Fig 7 Shows that there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula VI compared to standard chemo therapeutic drug Cisplatin

Fig 8 shows that there is decrease in percentage viability of spheres of PC3 in presence of compound of Formula VI compared to standard chemotherapeutic drug Cisplatin.

Fig 9. Shows compound of Formula VII exhibits higher anticancer activity on MCF7, MDAMB231, PC3 and DU145 cell lines compared to standard chemo therapeutic drug Cisplatin in MTT assay. Fig 10. Shows that compound of Formula VII exhibits higher anticancer activity on MDAMB231, PC3 cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay.

Fig.11 Shows there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula VII compared to standard chemo therapeutic drug Cisplatin.

Fig 12 Shows that there is decrease in percentage viability of spheres of PC3 in presence of compound of Formula VII compared to standard chemotherapeutic drug Cisplatin.

Fig 13 Shows that compound of Formula VIII exhibits higher anticancer activity on MCF7, MDAMB231, PC3 and DU145 cell lines compared to standard chemotherapeutic drug Cisplatin in MTT assay. Fig 14 Shows that compound of Formula VIII exhibits higher anticancer activity on MDAMB231, PC3 cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay.

Figure 15 shows that there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula VIII compared to standard chemo therapeutic drug Cisplatin.

Fig 16 shows that there is decrease in percentage viability of spheres of PC3 in presence of compound of Formula VIII compared to standard chemotherapeutic drug Cisplatin. Fig 17 Shows that compound of Formula ΓΧ exhibits higher anticancer activity on MCF7, MDAMB231, PC3, DU145 cell lines compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Fig 18 Shows compound of Formula IX exhibits higher anticancer activity on MDAMB231, PC3 cell lines compared to standard therapeutic drug Cisplatin in Soft Agar Assay.

Fig 19 Shows that there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula ΓΧ compared to standard chemo therapeutic drug Cisplatin.

Fig 20 indicates that there is decrease in percentage viability of spheres of PC3 in presence of compound of Formula IX compared to standard chemotherapeutic drug Cisplatin. Fig 21. Shows that compound of Formula X exhibits higher anticancer activity on MCF7, MDMB231, PC3, DU145 cell lines compared to standard chemo therapeutic drug Cisplatin in MTT assay.

Fig 22. Shows that compound of Formula X exhibits higher anticancer activity on MDMB231, PC3 cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay.

Fig 23 Shows that there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula X compared to standard chemo therapeutic drug Cisplatin. Fig 24 Shows that compound of Formula XI exhibits higher anticancer activity on MCF7, MDMB231, PC3, DU145 cell lines compared to standard chemo therapeutic drug Cisplatin in MTT Assay.

Fig 25 Shows that compound of Formula XI exhibits higher anticancer activity MDMB231, PC3 cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay.

Fig 26 Shows that compound of Formula XII exhibits higher anticancer activity on MCF7, MDMB231, PC3, DU145 cell lines compared to standard chemo therapeutic drug Cisplatin in MTT Assay

Fig 27 Shows that compound of Formula XII exhibits higher anticancer activity on MDMB231, PC3 cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay. Fig 28 Shows that percentage viability of spheres of MDAMB231 in presence of compound of Formula XII is similar compared to standard chemo therapeutic drug Cisplatin.

Fig 29 Shows that percentage viability of spheres of PC3 in presence compound of Formula XII is higher compared to standard chemotherapeutic drug Cisplatin.

Fig 30 Shows that compound of Formula XIII exhibits higher anticancer activity on MDMB231, PC3, DU145 cell lines compared to standard chemo therapeutic drug Cisplatin in MTT assay

Fig 31 Shows that compound of Formula XIII exhibits higher anticancer activity on MDMB231, PC3 cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay.

Fig 32 Shows there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula XIII compared to standard chemo therapeutic drug Cisplatin. Fig 33 Shows that there is decrease in percentage viability of spheres of PC3 in presence of compound of Formula XIII compared to standard chemotherapeutic drug Cisplatin.

Fig 34. Shows that compound of Formula XIV exhibits higher anticancer activity on MDMB231 cell line compared to standard chemo therapeutic drug Cisplatin in Soft Agar Assay. Fig.35 Shows that there is decrease in percentage viability of spheres of MDAMB231 in presence of compound of Formula XIV compared to standard chemotherapeutic drug Cisplatin.

Fig.36 Shows that there is decrease in percentage viability of spheres of PC3 in presence of compound of Formula XIV compared to standard chemotherapeutic drug Cisplatin.

DESCRIPTION OF THE INVENTION

The present invention relates to compounds for treating various conditions, particularly for inhibition of uncontrolled cell proliferation. Particularly the compounds are effective against cancer stem cells and treating cancer.

The present invention relates to compound of Formula 1 :

wherein, R ¹ is selected from -H, -CH ₂ OH; R ² is selected from— H, -OH, alkoxy, alkyl, acetyl, C ₃ -Cs acyl group; R is selected from alkoxy, alkyl, acetyl, C ₃ -Cs acyl group; R ⁴ is selected from -OH, F, -NH ₂ , -NHCGCH ₃ , alkyl, acetyl, C ₃ -C ₈ acyl group; R ⁵ is H, CI; R ⁶ and R ⁷ each independently is selected from H, alkyl, substituted or unsubstituted aromatic group, alkoxy, NH ₂ , N0 ₂ , -NHCOCH ₃ , -

6 7 8

CN, -0-, halogen, -OCF ₃ or R and R together form a heterocyclic ring; R is H, CI; R ⁹ is selected from a substituted or unsubstituted 5- or 6-membered ring, - CH ₂ -O CH ₂ -COOH R ¹⁰ is =0 or H; A is O, -NH, -N-alkyl; Q is O, S, -CH ₂ 0-; X is selected from CH ₂ , O, N, S; E is selected from CH, O, N, S; and Z is selected from CH, O, N, S. In one embodiment, the R ⁹ group is

In another embodiment of the present invention, a compound of formula II is provided:

Formula II

In an embodiment, the present invention provides compounds of Formula III or salts thereof for treating various conditions, particularly for inhibition of uncontrolled cell proliferation. Particularly, the compounds are effective against cancer stem cells.

Formula III

wherein, E and Z is selected from C, G, N, S, salts of N such as N. HCl; Q is O, S, -CH ₂ O-, -NY', wherein Y' is selected from -H, alkvl; SOOCH3; R ⁵ is -H, -CI, when E and/or 7. is -C; R ⁶ and R each independently is selected from -H, alkoxy, alkyl, substituted or unsubstituted aromatic group, -NH ₂ , -N0 ₂ , - NHCOCH ₃ , -CN, -0-, halogen, -OCF ₃ or R ⁶ and R ⁷ together form a heterocyclic ring; R ⁸ is -H, -CI, when E and/or Z is -C; R ₉ is -CH2-0— CH2, -COOH, -X where X can be F, CI, Br, alkyl such as -CH ₃ , -OH, alkoxy such as -OMe, NHCOCH ₃ , H, NH ₂ R ¹¹ and R ¹² each independently is selected from -FL R ¹¹ and R can be substituted or unsubstituted 5- or 6- membered ring such as lactone, -C(0)0-alkyl such as -CtO)OC ₂ H5 ; R is selected from:

SOO-CH ₃ , -SOQPh, , -CH ₂ C(0)N(CH ₃ ) ₂ , -C(0)NHPh, -C(0)NHPhOH, - C(S)NHPh, -CH ₂ PI1, -COAr, -SOOAr, -CONHAr, -CH ₂ Ar, -CSNHAr, wherein, R ¹³ is selected from -OH, -NH ₂ , -NHCOCH ₃ , X = F, CI, Br, alkyl, acetyl, C ₃ -Cg acyl group; R ¹⁴ is selected from alkoxy, -OMe, -OH, NH ₂ - NHCOCH _3, X - F, CI, Br, alkyl, acetyl, C ₃ -C ₈ acyl group; R ¹⁵ is selected from alkoxy, -OMe, -OH, -H, Br, NH ₂ , X ^~ F, CI, Br, alkyl, acetyl, C ₃ -C ₈ acyl group; R ¹⁶ is selected from -H, -CH ₂ OH, -OH, alkyl, alkoxy; R ¹⁷ is selected from alkyl. According to an embodiment of the present invention, a compound of Formula IV or salts thereof is provided to prevent cell proliferation:

Formula IV

wherein, R, R ⁶ , R', R ¹¹ and R ¹² have the meaning as assigned above.

In a preferred embodiment of the present invention, a compound of Formula V or salts thereof is provided to prevent cell proliferation:

Formula V

The compound of Formula V of the present invention are active on Breast and prostate cancer cell lines. Further, compound of Formula V is potent compared to standard chemotherapeutic drug Cisplatin. The compound of Formula V does not show activity on normal lymphocytes.

In another preferred embodiment of the present invention, a compound of Formula VI or salts thereof is provided to prevent cell proliferation:

Formula VI

Compound of Formula VI shows activity in breast and prostate cancer cell lines. Further, compound of Formula VI is potent compared to standard chemotherapeutic drug Cisplatin. The compound of Formula VI does not show activity on normal lymphocytes.

In an embodiment, the present invention provides compounds that demonstrate anticancer and anti-cancer stem cell activity particularly in breast and prostate cancer cell lines. In an embodiment, compound of formula VII is provided:

Formula VII

Compound of Formula VII shows activity in breast and prostate cancer cell lines. The compound of Formula VII does not show activity on normal lymphocytes.

In another embodiment, the present invention provides compound of Formula VIII that prevents cell proliferation.

Formula VHi

Compound of Formula VIII shows activity in breast and prostate cancer cel l lines and does not show activity on normal lymphocytes.

In a further embodiment of the present invention compound of Formula IX is provided that prevents cell proliferation:

Formula IX

Compound IX of the present invention shows activity in breast and prostate cancer cell lines.

In yet another embodiment of the present invention, compound of Formula X is provided that prevents cell proliferation:

Formula X

Compound of formula X shows activity in breast and prostate cancer c lines and does not show activity in normal lymphocytes.

In yet another embodiment, the present invention provides compound Formula XI that prevents cell proliferation:

Formula XI

Compound of formula XI . shows acti vity in breast and prostate cancer cell lint

In yet another embodiment, the present invention provides compound Formula XII that prevents cell proliferation;

Formula XII

Compound of formula XII shows activity in breast and prostate cancer cell lines. In a further embodiment, the present invention provides compound of Formula XIII that prevents cell proliferation:

Formula XIII

Compound of formula XIII shows activity in breast and prostate cancer cell lines.

In a further aspect, a compound of Formula XIV is provided:

Formula XIV

Compound of formula XIV shows activity in breast cancer cell lines

In an embodiment of the present invention, compounds of formula V to XIV of the present invention for use in the treatment of cancer is provided. Preferably, the compound of Formula V and VI are provided for use in the treatment of cancer. The cancer can be the cancer is breast, oral, prostate, brain, blood, bone marrow, liver, pancreas, skin, kidney, colon, ovary, lung, testicle, penis, thyroid, parathyroid, pituitary, thymus, retina, uvea, conjunctiva, spleen, head, neck, trachea, gall bladder, rectum, salivary gland, adrenal gland, throat, esophagus, lymph nodes, sweat glands, sebaceous glands, muscle, heart, or stomach cancer. In a preferred embodiment, the compounds of Formula V and VI for use in the treatment of breast and/or prostate cancer is provided.

In a further embodiment, pharmaceutical compositions including the compounds of the present invention, pharmaceutically acceptable excipient including carrier, adjuvant, vehicle or mixtures thereof are provided. Preferably, pharmaceutical compositions including compounds of Formula V and VI pharmaceutically acceptable excipient including carrier, adjuvant, vehicle or mixtures thereof are provided. The pharmaceutical excipient can further include one or more binders, diluents, disintegrants, glidants, lubricants, stabilizers, surface active agents or pH- adjusting agents.

In certain embodiments, the amount of compound in compositions may be such that it is effective to treat cancer in a subject in the need thereof. In certain embodiments, the composition may comprise between the biologically effective dose and the maximum tolerated dose of the compound of the invention or it's pharmaceutically acceptable salt, ester, or salt of an ester.

In certain embodiments, a composition of this invention may be formulated for administration to a subject in the need thereof. The pharmaceutical compositions of the present invention may be formulated into a suitable dosage form to be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir. Compositions of the present invention may be formulated into dosage forms including liquid, solid, and semisolid dosage forms. The term "parenteral" as used herein includes subcutaneous, intravenous, intraperitoneal, intramuscular, intra- articular, intrasynovial, intrastemal, intrathecal, intrahepatic, intralesional and intracranial injection or infusion techniques. Preferably, the compositions are administered orally, intravenously or intraperitoneally.

The present invention also includes the composition including the compounds of the present invention of Formula V to XIV, preferably compound of Formula V or VI for use in the treatment of cancer including cancer is breast, oral, prostate, brain, blood, bone marrow, liver, pancreas, skin, kidney, colon, ovary, lung, testicle, penis, thyroid, parathyroid, pituitary, thymus, retina, uvea, conjunctiva, spleen, head, neck, trachea, gall bladder, rectum, salivary gland, adrenal gland, throat, esophagus, lymph nodes, sweat glands, sebaceous glands, muscle, heart, or stomach cancer. In a preferred embodiment, the composition of the present invention is for the treatment of breast, and/or prostate cancer.

In certain embodiments of the present invention disclose a formulation comprising the compounds of the present invention along with other active agents or pharmaceutically acceptable excipients, etc.

In an embodiment, a pharmaceutical composition comprises the aforesaid compounds with another active agent such as but are not limited to imatinib, nilotinib, gefitinib, sunitinib, carfilzomib, salinosporamide A, retinoic acid, cisplatin, carboplatin, oxaliplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide, azathioprine, mercaptopurine, doxifluridine, fluorouracil, gemcitabine, methotrexate, tioguanine, vincristine, vinblastine, vinorelbine, vindesine, podophyllotoxin, etoposide, teniposide, tafluposide, paclitaxel, docetaxel, irinotecan, topotecan, amsacrine, actinomycin, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, plicamycin, mitomycin, mitoxantrone, melphalan, busulfan, capecitabine, pemetrexed, epothilones, 13-cis- etinoic Acid, 2-CdA, 2-Chlorodeoxyadenosine, 5- Azacitidine, 5 -Fluorouracil, 5-FU, 6-Mercaptopurine, 6-MP, 6-TG, 6- Thioguanine, Abraxane, Accutane, Actinomycin-D, Adriamycin, Adrucil, Afinitor, Agrylin , Ala-Cort, Aldesleukin, Alemtuzumab, ALIMTA, Alitretinoin, Alkaban-AQ, Alkeran, All-transretinoic Acid, Alpha Interferon, Altretamine, Amethopterin, Amifostine, Aminoglutethimide, Anagrelide, Anandron, Anastrozole, Arabinosylcytosine, Ara-C, Aranesp, Aredia, Arimidex, Aromasin, Arranon, Arsenic Trioxide, Arzerra, Asparaginase, AT A, Avastin, Azacitidine, BCG, BCNU, Bendamustine, Bevacizumab, Bexarotene, BEXXAR, Bicalutamide, BiCNU Aromasin, Blenoxane, Bleomycin, Bortezomib, Busulfan, Busulfex, C225, Calcium Leucovorin, Campath, Camptosar, Camptothecin-11, Capecitabine, Carac, Carboplatin, Carmustine, Carmustine Wafer, Casodex, CC- 5013, CCI-779, CCNU, CDDP, CeeNU, Cerubidine, Cetuximab, Chlorambucil, Citrovorum Factor, Cladribine, Cortisone, Cosmegen, CPT-11, Cytadren, Cytosar-U, Cytoxan, Dacarbazine, Dacogen, Dactinomycin, Darbepoetin Alfa, Dasatinib, Daunomycin, Daunorubicin Hydrochloride, Daunorubicin Liposomal, DaunoXome, Decadron, Decitabine, Delta-Cortef, Deltasone, Denileukin, Diftitox, DepoCyt, Dexamethasone, Dexamethasone Acetate, Dexamethasone Sodium Phosphate, Dexasone, Dexrazoxane, DHAD, DIC, Diodex, Docetaxel, Doxil, Doxorubicin, Doxorubicin Liposomal, Droxia, DTIC, DTIC-Dome, Duralone, Efudex, Eligard, Ellence, Eloxatin, Elspar, Emcyt, Epirubicin, Epoetin Alfa, Erbitux, Erlotinib, Erwinia L-asparaginase, Estramustine, Ethyol, Etopophos, Etoposide, Etoposide Phosphate, Eulexin, Everolimus, Evista, Exemestane, Fareston, Faslodex, Femara, Filgrastim, Floxuridine, Fludara, Fludarabine, Fluoroplex, Fluorouracil, Fluorouracil (cream), Fluoxymesterone, Flutamide, Folinic Acid, FUDR, Fulvestrant, G-CSF, Gefitinib, Gemcitabine, Gemtuzumab, ozogamicin, Gemzar Gleevec, Gliadel Wafer, GM-CSF, Goserelin, Granulocyte - Colony Stimulating Factor, Granulocyte Macrophage Colony Stimulating Factor, Halotestin, Herceptin, Hexadrol, Hexalen, Hexamethylmelamine, HMM, Hycamtin, Hydrea, Hydrocort Acetate, Hydrocortisone, Hydrocortisone Sodium Phosphate, Hydrocortisone Sodium Succinate, Hydrocortone Phosphate, Hydroxyurea, Ibritumomab, Tiuxetan, Idamycin, Idarubicin If ex, IFN- alpha, Ifosfamide, IL-11, IL-2, Imatinib mesylate, Imidazole Carboxamide, Interferon alfa, Interferon Alfa-2b (PEG Conjugate), Interleukin-2, Interleukin-11, Intron A (interferon alfa-2b), Iressa, Irinotecan, Isotretinoin, Ixabepilone, Ixempra , Kidrolase , Lanacort , Lapatinib, L-asparaginase, LC , Lenalidomide, Letrozole, Leucovorin, Leukeran, Leukine , Leuprolide, Leurocristine, Leustatin, Liposomal Ara-C, Liquid Pred , Lomustine, L-PAM, L-Sarcolysin, Lupron , Lupron Depot , Matulane , Maxidex, Mechlorethamine, Mechlorethamine Hydrochloride, Medralone , Medrol , Megace , Megestrol, Megestrol Acetate, Melphalan, Mercaptopurine, Mesna, Mesnex , Methotrexate, Methotrexate Sodium, Methylprednisolone, Meticorten , Mitomycin, Mitomycin-C, Mitoxantrone, M-Prednisol , MTC, MTX, Mustargen , Mustine, Mutamycin , Myleran , Mylocel, Mylotarg , Navelbine , Nelarabine, Neosar , Neulasta , Neumega , Neupogen , Nexavar , Nilandron , Nilotinib, Nilutamide, Nipent , Nitrogen Mustard, Novaldex , Novantrone , Nplate, Octreotide, Octreotide acetate, Ofatumumab, Oncospar , Oncovin , Ontak , Onxal, Oprelvekin, Orapred , Orasone , Oxaliplatin, Paclitaxel, Paclitaxel Protein-bound, Pamidronate, Panitumumab, Panretin , Paraplatin , Pazopanib, Pediapred , PEG Interferon, Pegaspargase, Pegfilgrastim, PEG-INTRON , PEG- L-asparaginase, PEMETREXED, Pentostatin, Phenylalanine Mustard, Platinol , Platinol-AQ , Prednisolone, Prednisone, Prelone , Procarbazine, PROCRIT , Proleukin , Prolifeprospan 20 with Carmustine Implant, Purinethol , Raloxifene, Revlimid , Rheumatrex , Rituxan , Rituximab, Roferon-A (Interferon Alfa-2a), Romiplostim, Rubex , Rubidomycin hydrochloride, Sandostatin , Sandostatin LAR , Sargramostim, Solu-Cortef , Solu-Medrol , Sorafenib, SPRYCEL , STI- 571, Streptozocin, SU11248, Sunitinib, Sutent, Tamoxifen, Tarceva , Targretin , Tasigna , Taxol , Taxotere , Temodar , Temozolomide, Temsirolimus, Teniposide, TESPA, Thalidomide, Thalomid , TheraCys , Thioguanine, Thioguanine Tabloid , Thiophosphoamide, Thioplex , Thiotepa, TICE , Toposar , Topotecan, Toremifene, Torisel , Tositumomab, Trastuzumab, Treanda , Tretinoin, Trexall , Trisenox , TSPA, TYKERB , VCR, Vectibix , Velban , Velcade , VePesid , Vesanoid , Viadur , Vidaza , Vinblastine, Vinblastine Sulfate, Vincasar Pfs , Vincristine, Vinorelbine, Vinorelbine tartrate, VLB, VM- 26, Vorinostat, Votrient, VP- 16, Vumon , Xeloda , Zanosar , Zevalin , Zinecard , Zoladex , Zoledronic acid, Zolinza, Zometa , or combinations of any of the above.

In yet another embodiment, a method of treating cancer by administering an effective amount of compounds V to XIV of present invention is provided. In a preferred embodiment, a method of treating cancer comprising administering an effective amount of compound of formula V or VI is provided. The cancer can be breast, oral, prostate, brain, blood, bone marrow, liver, pancreas, skin, kidney, colon, ovary, lung, testicle, penis, thyroid, parathyroid, pituitary, thymus, retina, uvea, conjunctiva, spleen, head, neck, trachea, gall bladder, rectum, salivary gland, adrenal gland, throat, esophagus, lymph nodes, sweat glands, sebaceous glands, muscle, heart, or stomach cancer. In a preferred embodiment, the method of treatment of the present invention comprising administering an effective amount of compound of Formula V or VI can be for the treatment of breast and/ or prostate cancer.

In an embodiment, a method of inhibition of unregulated cell growth by administering effective amount of the compounds of the present invention is provided.

In a further embodiment, the method of treating cancer by administering compounds of the present invention along with standard therapies or in combination with other drugs available for the treatment of cancer.

Another embodiment of the invention provides for the use of the compounds in the treatment of unregulated cell growth, malaria, dengue.

The foregoing description of the invention has been set merely to illustrate the invention and is not intended to be limiting. Since modifications of the disclosed embodiments incorporating the spirit and substance of the invention may occur to person skilled in the art, the invention should be construed to include everything within the scope of the disclosure. Following are the illustrative and non-limiting examples, including the best mode, for practicing the present invention. EXAMPLE 1:

Synthetic scheme for Diphyllui derivatives

Scheme I

Scheme I): i) Br ₂ , AcOH at room temperature, ii) Ethylene glycol, Toluene, p- Toluenesulphonic acid (PTSA), reflux, iii) n-BuLi, Aldehyde, -78°C, iv) Diethylacetylenedicarboxylate (DEADC), methylene dichloride (MDCO, 140°C, v) L1AIH ₄ , Tetrahydrofuran (THF).

Procedure:

Synthesis of 2: Substituted aromatic aldehyde (0.3 mole) was taken in AcOH (200 mL) and Br ₂ (0.6 mole) was added slowly from addition funnel. The mixture was stirred for 3h at room temperature and then poured over ice (100 g) and stirred vigorously for 30 min. Slurry was filtered and residue was washed with cold methanol and suction dried under vacuum to obtain pure product 2. Yield, 0.25 mole (85%).

Synthesis of 3: Compound 2 (O. l lmole) was dispersed in 350 mL of toluene. Ethylene glycol 70 mL and p-Toluenesulphonic acid (0.5 g) were added and mixture was refluxed using Dean-stark assembly for 5h. Reaction was monitored with TLC (3:7, Ethyl acetate: Hexane). After completion of reaction, saturated NaHC0 ₃ solution was added into the reaction and layers were separated. Toluene layer was washed with brine and dried over anhydrous Na2S04. Dried toluene layer was evaporated in vacuum to afford pure product 3 (O. l lmole, 97%).

Synthesis of 4: In an inert reaction assembly charged with nitrogen compound 3 (0.034 mole) was dissolved in Dry THF (150mL). Mixture was then cooled in a dry ice/acetone bath till -65°C. Through transfer needle 50 ml n-BuLi (1.6M solution in hexane) was added carefully and slowly into the above solution over 30 min. Mixture was stirred for lh at -65°C. In a separate addition funnel, the solution of R -CHO in THF was added drop wise in to the lithiated solution at - 65°C. Mixture was stirred for 30 min at same temperature and left at room temperature for 2h. Mixture was quenched with lOmL sat. NH ₄ C1 solution and extracted with ethyl acetate (200mL x 2). Ethyl acetate layer was washed with brine solution (lOOmLx 2), dried over anhydrous Na ₂ S0 ₄ and evaporated in vacuum to isolate crude product. Purification by column chromatography (in silica gel, Ethyl acetate: hexane) gave pure product 4 (O.OOSmole, 24%). Synthesis of 5: Compound 4 (0.012 mole), acetic acid (6.7mL), DEADC (0.016 mole) and MDC (lOOmL) were taken into the high pressure closed vessel. Mixture was heated at 140°C for 2h. Heating stopped and mixture was washed with saturated NaHC0 ₃ . MDC layer was dried with anhydrous Na ₂ S0 ₄ and solvents were evaporated in vacuum and crude product was purified by silica gel column chromatography in ethyl acetate: hexane as a mobile phase. Pure product 5 obtained as an off white solid (0.016 mole, 93%).

Synthesis of 6: Ester 5 (0.0021 mole) was dissolved in dry THF and slowly added into the dispersion of LiAlH ₄ (0.0042 mole) in THF at 0°C. Mixture was stirred at 0°C for 2h and then at room temperature for overnight. Reaction was quenched with saturated NH ₄ C1 and product was extracted with MDC. Crude product was purified by column chromatography to obtain pure product 6 (0.0011 mole).

Synthesis of Glycoside portion

Scheme II Scheme II, Synthesis of Glycoside: a) Ac-Cl, Pyridine, room temperature, b) HBr/AcOH, 0°C, c) TBAB, 2,6-lutidine, EtOH, d) NaOME, MeOH, e) NaH, DMF, Mel, f) i) AcOH ii) AcCl, Pyridine, g) HBr/AcOH, MDC

Synthesis of tetra-acylated d-xylose (7): D-xylose (0.13mole) was mixed in MDC (lOOmL) and pyridine at room temperature. Mixture cooled to 0°C and acetyl chloride (0.78 mole) was added slowly under vigorous stirring. Mixture stirred for lh at 0° and then at room temperature for 3h. 50gm crushed ice was added into the mixture and then 200mL MDC. Layers were separated and MDC extract was washed with brine solution (lOOmL x 2) and 10% aq. CuS0 ₄ solution until original CuS04 solution color persists. MDC layer was dried over anhydrous Na ₂ S0 ₄ and evaporated in vacuum on rotary evaporator to obtain the syrupy product 7 (0.129 mole, 97%).

Synthesis of 8: In a clean and dry round bottom flask, with nitrogen inlet, compound 7 (0.129 mole) was dissolved in 200mL dry MDC. Mixture cooled to 0°C in an ice bath and lOOmL HBr/AcOH (33% solution) was added drop wise over a period of 30min. Material stirred for 2h at 0°C and quenched with 50g ice and stirred for 10 min. MDC layer was separated and washed with sat. NaHC0 ₃ (lOOmL x 3), brine (lOOmL) and dried over anhydrous Na ₂ S0 ₄ and evaporated in vacuum on rotary evaporator to obtain the off-white solid product 8 (0.097mole, 76%).

Synthesis of 9: Above compound 8 was taken directly into another round bottom flask containing TBAB (0.040 mole), 2, 6-Lutidine (0.129 mole) and MDC 200mL and stirred at room temperature for lh. After lh stirring 6.5mL EtOH was added slowly and stirring continued for overnight. Solvent removed on rotary evaporator and residue triturated in ethyl acetate (200mL). Solids were removed by filtration and filtrate was evaporated. Syrupy crude product was purified by silica gel column chromatography in ethyl acetate: hexane to obtain semisolid pure product 9 (0.049 mole, 51%).

Synthesis of 10: In a single neck round bottom flask compound 9 (0.049 mole) was dissolved in MeOH at room temperature. This mixture cooled between 15- 10°C and NaOMe (600mg) was added in small portions over 10 min and then stirred for 2h at room temperature. Thin Later Chromatography (TLC) confirmed the de-acylated product formation. Methanol evaporated on rotary evaporator and residue was dissolved in dry DMF (100 mL). DMF solution chilled to 0°C and NaH (6 g, 60% suspension) was added portion wise under vigorous stirring under nitrogen atmosphere. Suspension stirred for 15 min at same temperature and methyl iodide was added slowly. Whole suspension was stirred overnight at RT. When TLC confirmed the product formation, 2 mL MeOH and crushed ice, (150g) were added slowly. Reaction mixture was extracted with ethyl acetate (200 mL x 2). Combined ethyl acetate extract was washed with saturated brine solution (50 mL x 4) dried over an. Na2S04 and evaporated on rotary evaporator to obtain oily liquid product 10 (0.048 mole, 98%).

Synthesis of 11: Compound 10 (0.048 mole) was dissolved in gl. AcOH (50 mL) at 0°C and stirred for lh at room temperature. Acetic acid was evaporated and obtained syrupy residue was dissolved in pyridine (100 mL) and cooled up to 0°C. Ac-Cl was slowly charged into the chilled solution and stirred at room temperature for overnight. Into the reaction mixture 50mL chilled water was added and extracted with diethyl ether (100ml x 2). Ether extract was washed with sat. CuS0 ₄ solution (50ml x4) and brine (50ml) dried over An. Na ₂ S0 ₄ and evaporated on rotary evaporator to isolate product 11 (0.038mole, 79%)

Synthesis of 12: In 100ml dry MDC 11 (0.015 mole) was added and chilled upto 0°C. lOmL HBr/AcOH (33% solution) was added slowly and mixture was stirred for lh at 0°C. Crushed ice (20g) was added in to the reaction stirred for 5min. MDC layer was washed with sat. NaHC0 ₃ solution (50mL x 4), brine (50ml) and dried over Na ₂ S0 ₄ and resulting solution used as such for the synthesis of 13 (see scheme III).

Coupling of diphyl n derivative (6) and glycoside moiety (12)

Scheme III

Scheme III: i) 2N NaOH, TBAB, MDC ii) MeOH, K ₂ C0 ₃ Synthesis of 13: Diphyllin derivative (6, 0.0065 mole), TBAB (0.006 mole) and 2N NaOH (25mL) were mixed in MDC (50mL) at 0°C. To this, above prepared solution of 13 in MDC was added slowly. Reaction was stirred for 1.5h and TLC confirmed the product formation. Into the reaction, 25mL ice cold water was added and stirred vigorously, and then organic phase was separated. MDC layer was washed with 2N NaOH, water, brine and dried over Na ₂ S0 ₄ evaporated on rotary evaporator to obtain crude 13 (2.3g). Crude product was purified by silica gel column chromatography in Ethyl acetate: Hexane from which pure compound 13 (0.0020mole) was isolated. Synthesis of 14: Condensation product 13 (0.0020 mole) from Glycoside and diphyllin derivative was dissolved in MeOH and chilled the solution till 0°. To this solution anhydrous K ₂ C0 ₃ was added and stirred for lh at room temperature. TLC shows complete conversion of 13 into the product 14. Aq. HC1 (IN) was added to adjust the neutral pH and MDC was added to extract the product. MDC layer was washed with brine and dried over Na ₂ S0 ₄ and evaporation of MDC on rotary evaporator afforded crude product, which was purified by silica gel column chromatography in Ethyl acetate: Hexane. Pure product 14 (0.00092 mole, 46%) was obtained with >98% purity.

EXAMPLE 2 Synthesis of compound of Formula V (numbered as 14 in Scheme 3)

Step I: Synthesis of 4-(benzo[d][l,3]dioxol-5-yl)naphthalen-l-ol

Scheme 1

Reagents and conditions: a) NBS ^' (N-BromosuccinimicSe), ACN (Acetonitrile, RT, 1,5 hr; b) PhCiTBr, K ₂ CQ ₃ , DMF (Dimethylfomianiide); c) Pd(PPh ₃ )4- 3,4- (rnethylenedioxy). phenylboronie acid, jCOs, DME (Dimethoxyetharse); d) 10% Pd/e, EtOH:EtQAc (1 : 1) _. , 60 °C, 60-80 psi.

Experiments:-

Synthesis of4~hromofi phihalen~l~ol (2):

To a solution of 1 (5 g, 34,7 mmol) in 180 niL of ACN, NBS (6.18 g, 34.7 mmol) was added over a period of 1 hi". The reaction mixture was stirred at RT for additional 30 min and monitored using TLC. The solvent was evaporated and the residue was partitioned I;n diethyl ether and water. The- ethereal layer was dried over anhydrous sodium, sulfate and concentrated under reduced pressure. Synthesis of I~0enz}doxy)~4-hr m ,aphth iene (3):

To a solution of 2 (7 g, 31.4 mmol) in DMF, K2CO3 (8,9 g, 64.44 mmol) was added followed by slow addition of benzyl bromide (3.-98 mL, 33,5 mmo-l). The reaction .mixture was stirred at RT and monitored using TLC. After completion, reaction was. quenched with brine and the residue was extraeted using ethyl acetate and washed with water. ^" The combined organic layer was dried oyer anhydrous sodium sulfate and concentrated under reduced pressure. The obtained solid was purified by column chromatography (Hex: EtOAc, 98:2). Synthesis of 5-(4-(benzyloxy) naphthalen-l-yl)benzo[d][l,3]dioxol (4):

To a solution of 3 (1 g, 3.2 mmol) in DME, Pd(PPh ₃ ) ₄ (0.184 g, 5 mol %) was added and stirred for 30 min at T. The suspension of 3, 4- (methylene dioxy) phenylboronic acid (0.635 g, 3.82 mmol) in DME was added to the above solution followed by addition of 2M Na ₂ C0 ₃ (0.676 g) solution. The reaction mixture was refluxed overnight, and monitored using TLC after completion, cooled to RT and solvent was distilled off. The residue was treated with aq. NH ₄ CI solution and extracted in ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained solid was purified by column chromatography (Hexane: DCM, 95:5)

Synthesis of 4-fl)enzo[d][l,3]dioxol-5-yl)naphthalen-l-ol (5):

A mixture of 4 (1 g, 2.82 mmol), 10% Pd/C in 50 mL of mixture of EtOH: EtOAc (1 : 1) was placed in shaker hydrogenation apparatus at 60 °C and 60-80 psi. The reaction was monitored using TLC. After completion, Pd/C was filtered off and the filtrate was evaporated. The obtained solid was purified by column chromatography (DCM: MeOH, 99: 1)

Step II: Synthesis of 2-0-Acetyl-3,4-dimethoxy-a-D-bromoxylopyranose (12): Scheme 2

Reagents and conditions: a) AC2O, pyridine; b) HBr*AcOH, DC (Dichioromet ane); c) 2,6-iutidine, Bu ₄ NBr, EtGH, DCM; d) 1. MeONa, Me OH; 2. NaH, Mel, DMF (Dimethyiformamide); e) AeOH, Ac ₂ 0 _; Pyridine; ;f) HBfAcQH, DCM

Synthesis of Tetr -O-acetyl-D-Aykpyranos (7):

To a 500-mL three-neck RBF equipped with guard-tube and stopper, were added 6 (40.0 g, 0.266 moi), pyridine (200 mL) and cooled at 0 °C. Acetic anhydride (200 mL) was added dropwis© to th above- mixture at 0 °C. Th resulting ^• reaction mixture was stirred, at- 0 °C for 5 h. After consumption of starting materials, as judged by TLC (5:5. EtO Ac: Hexane), reaction mixture was poured into ice water (500 mL) and ether was added (200 mL), Organic layer was separated, and aqueous, layer was extracted with ether (2 x. 250 mL). Organic layers were combined and washed with saturated cupric salt solution, till free from pyridine, lire organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to give sticky solid compound 7. Ή-NM (300 MHz, CDC1 ₃ ): δ = 6.27 (d, IH, J = 3.6 Hz), 5.70 (t, IH, J = 9 Hz), 5.06 (m, 2H), 3.97 (dd, IH, J =6.0, 1 1.1 Hz), 3.72 (t, IH, J = 1 1.0 Hz), 2.18 (s, 3H), 2.07(s, 6H), 2.03 (s, 3H).

Synthesis of2,3,4-Tri-0-acetyl-a-D-bromoxylopyranose (8):

1 L- BF with guard tube was charged with 7 (25.0 g, 78.54 mol) and dichloromethane (500 mL) and the mixture was cooled to 0 °C in ice bath. To the above cold solution was added hydrogen bromide (33 % in acetic acid; 56 mL) with constant stirring during 1 h and reaction mixture was further stirred at room temperature for 1 h. After completion of reaction as judged by TLC (4:6, EtOAc: Hexane), reaction mixture was washed with ice water (1 x 500 mL), 1 % NaHC0 ₃ solution (1 x 500 mL), 10 % NaHC0 ₃ solution (2 x 500 mL) and finally by brine solution (1 x 500 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtained white solid of 8.

1H-NMR (300 MHz, CDC13): δ = 6.59 (d, IH, J= 3.9 Hz), 5.60 (t, IH, J= 9.9 Hz), 5.05- 5.03 (m, IH), 4.77 (dd, IH, J= 3.9, 9.6 Hz), 4.07 (dd, IH, J= 6.3, 11.4 Hz), 3.88 (t, IH, J= 11.1 Hz), 2.10 (s, 3H), 2.06 (s, 6H).

Synthesis of 3 _f 4-Di-0-acetyl-l,2-0-(l-ethoxyethylidene)-D-xylopyranos e (9):

Two necked RBF were charged with 8 (25.0 g, 73.71 mmol), 2,6-lutidine (11.07 mL, 95.82 mmol), tetrabutyl ammonium bromide (9.50 g, 29.48 mmol) and anhydrous dichloromethane (147 mL). To the above mixture was added absolute ethanol (4.7 mL, 81.08 mmol) and reaction mixture was stirred at room temperature under nitrogen atmosphere for overnight. After completion of reaction as judged by TLC (5:5, EtOAc: Hexane), the reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography over silica gel using EtOAc: Hexane as eluent to afford 9 as a pale yellow colored liquid.

1H-NMR (300 MHz, CDC13): δ = 5.57 (d, 1H, J =4.2 Hz), 5.24 (t, 1H, J= 3.6 Hz), 4.84- 4.82 (m, 1H), 4.20 (t, 1H J= 1.8 Hz), 3.89 (dd, 1H, J= 5.1, 12.3 Hz), 3.71 (dd, 1H, J = 6.9, 12.3 Hz), 3.59 (q, 2H, J = 6.9 Hz ), 2.10 (s, 3H), 2.08 (s, 3H), 1.19 (t, 3H, J = 6.9 Hz).

In a dried RBF (250 mL) was charged with 9 (10 g, 32.86 mmol) and anhydrous methanol (157 mL) was added. To the above solution was added catalytic amount of sodium methoxide (300 mg) and stirred at room temperature for 1 h. After the completion of reaction as judged by TLC, reaction mixture was concentrated under reduced pressure and residue was dried under high vacuum. The resulting residue was dissolved in anhydrous DMF (100 mL) and cooled to 0 °C in ice-bath. To the above cold solution, sodium hydride (3.94 g, 60% dispersion in oil, 164.3 mmol) was added and resulting suspension was with stirring for 1 h. Methyl iodide (12.4 mL, 197.6 mmol) was added dropwise at 0 °C, the reaction mixture was then slowly brought to room temperature during 1 h and further stirred at room temperature for 12 h. After completion of reaction, reaction was quenched by addition of methanol (10 mL), diluted with ethyl acetate (100 mL), washed with water (2 x 50 mL), brine solution (1 x 50 mL) and dried over anhydrous sodium sulfate. The inorganic salts were filtered off, filtrate was concentrated under reduced pressure and residue was purified by column chromatography using EtOAc: Hexane (10:90) to afford 10 as a light yellow colored liquid.

1H-NMR (300 MHz, CDC13): 5 = 5.56 (d, 1H, J = 4.8 Hz), 4.29-4.26 (m, 1H), 3.89 (dd, 1H J= 3.3, 12.1 Hz), 3.82-3.69 (m, 5H), 3.54 (s, 3H), 3.44 (s, 3H), 3.26 (m, 1H), 1.19 (t, 3H, 6.9 Hz).

Synthesis of 1 ,2-Di-0-acetyl-3 _f 4-dimethoxy-D-xylopyranose (11):

10 (7.5 g, 30.20 nimol) was dissolved in acetic acid (55 mL) and resulting solution was stirred at 0 °C for 1 h. Reaction mixture was concentrated under reduced pressure and the residue was treated with acetic anhydride (26 mL) and pyridine (26 mL). The resulting solution was maintained at room temperature with stirring for overnight. After completion of reaction as judged by TLC (3:7, EtOAc: Hexane), reaction mixture was poured into cold water (100 mL) and extracted with ether (4 x 100 mL). The organic layers were combined, washed with saturated cupric sulfate solution till the pyridine was removed and then dried over anhydrous sodium sulfate. The inorganic solids were filtered off, filtrate was concentrated under reduced pressure and residue was purified by column chromatography over silica gel using EtOAc: Hexane (20:80) as eluent to afford 11 as a light yellow color.

1H-NMR (300 MHz, CDC13): 5 = 5.62 (d, 1H, J= 12 Hz), 4.95 (t, 1H J= 7.8 Hz), 4.1 1 (m, 1H), 3.57 (s, 3H), 3.48(s, 3H), 3.39-3.31 (m, 3H), 2.10(s, 3H), 2.09(s, 3H).

Synthesis of2-0-Acetyl-3,4-dimethoxy-a-D-bromoxylopyranose (12): In a clean and dry 50 nVL RBF, 11 (1.0 g, 3.81 ramoS) was dissolved in dichloromethane (25 mL) and cooled to 0 °C in ice bath.. To the above cooled solution was added hydrogen bromide in AcOH (33% solution ^' ; 2.5 mL) with constant stirring for 1 h and further stirred at room temperature for another 1 h. Afte completion of reaction as judged by TLC (3:7, l¾()Ac: Hexane), reaction mixture was diluted with dichloromethane (50 mL), washed with ice water (50 mL) followed b saturated NaHCOi solution (50 mL) and finally with brine solution (50 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to give yellow colored liquid 12 as a product.

lH-NMR (300 MHz, CDC 13): δ = 6.56 (d 1H _S J= 3.9 Hz), 4.56 (dd, 1R J= 3.9, 9.6 Hz), .00 (dd, HI, J = 6,3, 1 1.7, Hz), 3.72 (m, 1H), 3.5.6(s, 3H), 3.54 (s, 3H), 3.38 (m, 2H), 2J 3 (s, 3H).

Step III: Synthesis of(3R _r 41l,51l)-2~(4~{henz0[dI L3 iUoxoi~5

yloxy)~4, S-dimelh oxyte rahydro-2H~pyr n-3-ol (14)

S

Reagents and conditions: a) BU ₄ NB1-, 2M NaOH, DCM (Dichloromethane), RT; b) K ₂ CO ₃ MeOH, RT. b) K ₂ C0 ₃ MeOH, RT.

Synthesis of (3R,4S,5R)-2-(4-(benzo[d][l,3]dioxol-5-yl)naphthalen-l-yloxy )- 4,5-dimethoxy-tetrahydro-2H-pyran-3-yl acetate (13):

To a 50 mL RBF, 5 (0.208 g, 0.788 mmol), 12 (0.446 g, 1.576 mmol) and tetrabutyl ammonium bromide (0.254 g, 0.788 mmol) were taken in dichloromethane (20 mL) with stirring. To this suspension was added 2M NaOH (3 mL) solution and stirring was continued for 2 h at room temperature. After the completion of reaction as judged by TLC (1 :9, EtOAc: DCM), the reaction mixture was extracted with dichloromethane (4 x 20 mL). The combined organic layer was washed with 10% NaOH solution (3 x 15 mL) followed by water (2 x 10 mL) and dried over anhydrous sodium sulfate. Inorganic salts were filtered off; filtrate was concentrated under reduced pressure and crude mass which was purified by column chromatography using EtOAc: dichloromethane (4:96) as eluent to obtain 13 as white solid.

Synthesis of (3R,4R,5R)-2-(4-(benzo[d][l,3]dioxol-5-yl)naphthalen-l-yloxy )- 4,5-dimethoxy-tetrahydro-2H-pyran-3-ol (14):

To a solution of 13 (0.160 g, 0.343 mmol) in methanol (7.5 mL) was added solid anhydrous K ₂ C0 ₃ (0.0925 g 0.675 mmol) and reaction mixture was stirred at room temperature for 30 min. After completion of reaction as judged by TLC (5:5, EtOAc: Hexane), methanol was removed under reduced pressure, water was added and extracted with CH ₂ C1 ₂ (2 x 25 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to get 14 as white fluffy solid.

% Purity: 99%; LC-MS (ESI) m/z: 425 [M+H] ⁺

1H-NMR (400 MHz, CDC13): 5 = 8.35 (d, IH, J = 8 Hz), 7.89 (d, IH, J = 8 Hz), 7.51-7.46 (m, 2H), 7.31 (d, IH, J = 7.6 Hz), 7.14 (d, IH, J = 8.0 Hz), 6.94 (m, 3H), 6.03 (s, 2H), 5.52 (d, IH, J= 3.6 Hz), 4.18 (dd, IH, J = 6.3, 1 1.7. Hz), 4.05 (m, IH), 3.69 (s, 3H), 3.61 (m, 2H), 3.51 (s, 3H), 3.45 (m, IH), 3.38 (m, IH). EXAMPLE 3

Synthesis of compound of Formula VI (numbered as 26 in Scheme 4):

Synthesis of diethyl l-(benzofd]fl,3Jdioxol-5-yl)-4-((3R,4R,5R)-3-hydroxy-4,5- dimethoxy-tetrahydro-2H-pyran-2-yloxy)-6, 7-dimethoxynaphthalene-2,3- dicarboxyl te (26):

Scheme 4

Reagents and conditions: a) Bi^NBr, 2M NaOH, DCM (Dichloromethane),

RT; b) K ₂ C0 ₃ , MeOH, RT.

Experimental: Cley acetate (25):

To a 50-mL round bottom flask, diethyl l-(benzo[d] [l,3]dioxol-5-yl)-4-hydroxy- 6,7-dimethoxynaphthalene-2,3-dicarboxylate (19; 0.30 g, 0.638 mmole), 2-0- Acetyl-3,4-dimethoxy-a-D-bromoxylopyranose (12, 0.446 g, 1.276 mmole) and tetrabutyl ammonium bromide (0.254 g, 0.638 mmole) were taken in dichloromethane (20 mL) with stirring. To this suspension was added 2M NaOH (3 mL) solution and stirring was continued for 2 h at room temperature. After the completion of reaction as judged by TLC (1 :9, EtOAc:DCM), the reaction mixture was extracted with dichloromethane (4 x 20 mL). The combined organic layer was washed with 10% NaOH solution (3 x 15 mL) followed by water (2 x 10 mL) and dried over anhydrous sodium sulfate. Inorganic salts were filtered off, filtrate was concentrated under reduced pressure and crude mass which was purified by column chromatography 4 using EtOAc: dichloromethane (04:96) as eluent to obtain Cleyacetate (25) as an oil.

Synthesis of diethyl l-(benzo[d][l,3]dioxol-5-yl)-4-((3R,4R,5R)-3-hydroxy-4,5- dimethoxy-tetrahydro-2H-pyran-2-yloxy)-6, 7-dimethoxynaphthalene-2,3- dicarboxylate (26):

To a solution of 25 (0.20 g , 0.298 mmole) in methanol (7.5 mL) was added solid anhydrous K ₂ C0 ₃ (0.0825 g 0.597 mmol) and reaction mixture was stirred at room temperature for 30 min. After completion of reaction as judged by TLC (5:5, EtOAc:Hexane), methanol was removed under reduced pressure, water was added and extracted with CH ₂ CI ₂ (2 x 25 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to get 26 as off white fluffy solid.

Yield: 179 nig (96%% % Purity: 99%; LC-MS (ESI) ni/z: 629 [M+H

XHNMR (CDC13, 400 MHz): □ = 8.17 (s, 1H), 7.05 (d, 1 H, J = 1.5 Hz), 6.94 (dd, 1H. J - 1.2, 7.8 Hz), 6.98 (d, 2H, J- 1.6 Hz), 6.92 (d, 1H, J - 1.2 Hz), 6.80 (d, 1H _S J = 8 Hz), 6.12 ( .s, 2H), 5.73 ( m, 1 H), 5.50 (q, 2R J = 3.6 Hz), 5.00 (d, III J = 5.2 Hz), 4.80 (t, 1H, J = 6.8 Hz), 472 (d, 1H, J = 4.4 Hz), 3.94 (s., 3H), 3.86-3.81 (m, 311). 3.70 (s, 311). 3.51 (m, 1H), 3.46 (m, 1H).

EXAMPLE 4

Synthesis of com ound of Formula VII (numbered as 21 in Scheme 6) and compound of Formula VIII (referred as 22 in Scheme 7)

Siep I: Synthesis fD ^' iphyUin

Reagents and conditions: a) Br2, AcOH, 3 h; b) ethylene glycol, p-TSA (toluene sulfonic acid), toluene; c) n-BuLi, THF (tetrahydrofuran); d) piperinol, THF; e) diethyl acetylinedicarboxylate, AcOH, DCM; f) LiAlH ₄ , THF.

Experimental:

Synth esis of 2-Bromo-4, 5-dimeth oxybenzaldehyde (16):

Three necked BF (500 mL) equipped with dropping funnel, magnetic stirrer, and stopper was charged with veratraldehyde or 4,5-dimethoxybenzaldehyde (15, 15 g, 0.090 mol) and acetic acid (210 mL). To this solution was added bromine (9.67 mL) in acetic acid (60 mL) dropwise with constant stirring over half an hour and stirring was further continued for 3 h at room temperature. During this time all the starting materials was consumed as confirmed by TLC (3:7, EtOAc: Hexane). Water (250 mL) was added to the reaction mixture and cooled to 0 °C. The precipitated solid was filtered off, washed with cold water and dried under vacuum to get a white solid 16.

1H-NMR (CDC13, 300 MHz): δ = 10.19 (s, 1H), 7.43 (s, IH), 7.07 (s, 1H), 3.97 (s, 3H), 3.93 (s, 3H).

Synthesis of2-(2-Bromo-4,5-dimethoxyphenyl)- 1,3-dioxolane (17):

Three necked RBF (250 mL) was equipped with Dean-Stark apparatus and reflux condenser, was charged with 16 (19.0 g, 0.07 mol), toluene (200 mL), ethylene glycol (1.8 mL, 0.21 mol) and catalytic amount of p-toluene sulphonic acid. The reaction flask was immersed in oil bath and heated (90-95 °C) under reflux for 9 h (till all the water removed). After completion of reaction as judged by TLC (2:8, EtOAc: Hexane), reaction mixture was allowed to cool to room temperature, neutralized by sodium bicarbonate solution and extracted with ethyl acetate (3 x 100 mL). All the organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (5- 10%) in hexane as eluent to afford 17 as a white solid.

1H-NMR (300 MHz, CDC13): δ = 7.1 1 (s, 1H), 7.01 (s, 1H), 5.99(s, 1H), 4.18 (t, 2H, J = 6.9 Hz), 4.08 (t, 2H, J= 6.9 Hz), 3.89 (s, 3H), 3.88 (s, 3H).

Synthesis of (2-(l,3-Dioxolan-2-yl)-4,5-dimethoxyphenyl)(benzo[dJ [l,3]dioxol- 5-yl)-meth-anol (18):

To a flame dried three necked RBF (100 mL) were added 16 (1.0 g, 0.0034 mole) and anhydrous THF (25 mL) under nitrogen atmosphere. The flask was cooling to -78 °C in dry ice-acetone bath, n-BuLi (5.3 mL, 0.005 mol) was added dropwise with stirring at -78 °C and stirred for 15 min. A separate flame dried flask was charged with piperonal (0.517 g, 0.0034 mol) and dry THF (6 mL). The piperonal solution was cannulated to the reaction mixture during 30 min and after the addition; reaction mixture was slowly warmed to room temperature and further stirred for 2.5 h. After the consumption of all bromo compound, as confirmed by TLC (5:5, EtOAc: Hexane), reaction mixture was quenched by the addition of saturated ammonium chloride solution and extracted with ethyl acetate (3 x 20 mL). All the organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by titration with heptane and 18 is sufficiently pure to proceed to next step. Ή-NM (300 MHz, CDC13): δ = 7.14 (s, 1H), 6.90-6.78 (m, 4H), 6.1 1 (s, 1H ), 5.96 (s, 2H ), 5.90 (s, 1H), 4.19 (t, 2H, J= 6.6 Hz), 4.16 (t, 2H, J= 6.8 Hz), 4.02 (s, 3H), 3.81 (s, 3H), 3.17 (s, 1H ). 13C-NMR (300 MHz, CDC13): δ = 149.42, 148.1 1, 147.57, 146.58, 136.95, 135.43, 126.83, 121.04, 1 19.69, 1 1 1.48, 109.50, 107.92, 107.26, 101.65, 100.93, 71.34, 65.05, 55.94, 55.89.

Synthesis of Diethyl l-(3',4'-methylenedioxyphenyl)-4-hydroxy-6, 7-dimethoxy- naphthal ne -2,3-dic rboxylate (19):

Sealed tube was charged with 18 (0.30 g, 0.833 mmol), diethyl acetylinedicarboxylate (0.141 g, 0.833 mol), dichloromethane (0.4 mL) and glacial acetic acid (0.242 mL) and mixture was heated at 140 °C for 1 h. After completion of reaction as judged by TLC (5:5, EtOAc: Hexane), reaction mixture was cooled to room temperature, diluted with dichloromethane (10 mL), washed with 5 % sodium bicarbonate solution (3 x 10 mL), organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The crude reaction mass was purified by flash column chromatography over silica gel using EtOAc: Hexane (15:85) to afford 19 as white solid.

1H-NMR (300 MHz, CDC13): δ = 7.73 (s,lH), 6.89 (d, 1H, J = 7.8 Hz), 6.81- 6.75 (m, 3H), 6.05 (d, 2H, J= 14.4 Hz), 4.44 (q, 2H, J= 7.2 Hz), 4.07 (q, 2H, J =6.9 Hz), 4.05 (s, 3H), 3.77 (s, 3 H), 1.38 (t, 3H, J= 7.2 Hz), 1.08 (t, 3H, J= 6.9 Hz). 13C-NMR (300 MHz, CDC13): δ = 170.30, 168.74, 159.62, 152.37, 149.68, 147.22, 147.06, 132.21, 130.60, 128.99, 127.48, 124.37, 119.81, 1 1 1.42, 107.97, 105.73, 102.76, 101.09, 61.95, 60.81, 56.08, 55.79, 13.87, 13.82. Synthesis of 9-(3',4'-Methylenediox phenyl)-4-hydroxy-6, 7- dimethoxynaphtho[2,3-c]furan -l(3H)-one (20):

Two necked RBF (25 mL) was charged with LAH (0.032 g, 0.852 mmol) and anhydrous THF (4 mL) and the mixture was cooled to 0 °C with stirring. To this suspension, a solution of 19 (0.200 g, 0.426 mmol) in THF (4 mL) was added dropwise at 0 °C and stirring was continued for 2 h at same temperature. After completion of reaction as judged by TLC (1 :9, MeOH: DCM), reaction mixture was quenched with saturated sodium sulfate solution and extracted with t- butanol (4 x 20 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by flash column chromatography over silica gel to give yellow solid 20.

1H-NMR (300 MHz, DMSOd6) δ = 10.39 (s, 1H), 7.61 (s, I H), 7.00 (d, 1H, J= 8.1 Hz), 6.94 (s, 1H), 6.85 (d, 1H, J= 1.5 Hz), 6.75 (dd, 1H J= 1.5, 8.4 Hz), 6.10 (s, 2H), 5.35 (s, 2H), 3.93 (s, 3H), 3.64 (s, 3H). 13C-NMR (300 MHz, DMSOd6): δ = 169.81, 150.66, 149.89, 147.01, 146.76, 145.05, 129.71, 129.65, 128.95, 123.94, 123.45, 121.85, 1 18.86, 11 1.22, 108.02, 105.63, 101.19, 100.92, 66.71, 55.78, 55.29.

LC-MS (ESI) m/z: 381 [M+H]+

Step II: Synthesis of Diphyllin Esters

General procedure for Ester derivatives:

To a 50 mL RBF, 20 (1 eq.), corresponding carboxylic acid (1 eq.), DMAP (10 eq.) in 20 mL of DCM was cooled (at 0 °C). The reaction mixture was stirred for 30 min. and then DCC (1.1 eq. dissolved in cold DCM) was added dropwise. The reaction was stirred at RT overnight. The reaction was monitored using TLC (2:98, MeOH: DCM). After completion, the solid obtained was filtered off and the filtrate was diluted with DCM and washed with water twice, The combined organic layer was dried over Na ₂ S(¾ and concentrated under reduced pressure. 1¾e obtained solid was purified by column chromatography- (DCM; MeOH ^' , 98:2).

S nthesis f ^' 9-(benz [d][i,3]dioxel-5-yl)-6.7- dim4koxy~l~ax(i~i ^' ,3-iUhydronaphih [2,3~c furan~4~yl l-m thyl-lFI-pyrrole- 2~cathoxylate (21)

Scheme 6

20 21

Reagents and conditions; ^' a) l-methy!-2-pyrroleearboxylic acid, DMAP (4- Dimethy!amiiiopyrkline), DCC (Ν,Ν'-Dicyclohexyicarbodiimide), DCM (Dichloromethane), 0 ^C' C overnight.

Synthesis of 9-(h z [dj[l,3fdi0£ol-$-yl)-0 _f 7~dim thoxy~l~oxo-l,3~ dihydronapkth o[2, 3-cJfu.ran- 4-yl l-metkyl- lH-pyrrole~2~cafboxylate (21): To a 50 mL BF, Drphyllin (200 mg, 5.26 mraol), 1 -methyl- lH-pyrrole-2- carbox-ylie acid (65.78 mg, .5.26 mmol), DMAP (642 mg, 52.6 mmol.) in. 10 -mL of DCM was cooled (at 0 °C), The reaction mixture was stirred for 30 mia. and then DCC (119 mg, 5.78 mmol dissolved in cold. DCM) was added, dropwise. The reaction was stirred at RT overnight. The reaction was monitored using TLC (98:2, DCM:MeOH). After completion, the solid obtained was filtered off and the Filtrate was diluted with DCM and washed with water twice. The combined organic layer was dried over Na2S04 and concentrated under reduced pressure. The. obtained solid was purified by column chromatography (DCM:MeOH, 98:2).

% Purity: 99%; LC-MS (ESI) m/z: 488 [M+H] ⁺

lH-NMR (400 MHz, CDC13): 6 = 7.41 - 7.39 (m ₅ IH), 7.32 (s, 1H) _S 7.26 (s, IH), 7.13 (s. i l l ). 6.99 (m, 211), 6.86 (rn, 2H), 6.30 (ni. III), 6.10 (d, 711 J = 17.6 Hz), 5.32 (s, 2H), 4.01 (s, 3H), 3.98 (s, 3H). 3.81 (s, 3H).

Synthesis of ~ mzoj[d^ll 3 diax(^-5-yl)~6 _> 7~dim tho ^' xy~i-oxo-.li3~

dihydromaph ih of 2, 3-efiiran~4~yl 2~tyclopeniyl-2-ph nylac t ie {22} :

Scheme 7

20 22 Reagents and conditions: a) a-phenylcyclopentaneacetic acid, DMAP (4- Dimethylaminopyridine), DCC (Ν,Ν'-Dicyclohexylcarbodiimide), DCM (Dichloromethane), 0 °C overnight.

Synthesis of 9-(benzo[d][l,3]dioxol-5-yl)-6, 7-dimethoxy-l-oxo-l,3- dihydronaphtho[2,3-c]furan-4-yl 2-cyclopentyl-2-phenylacetate (22):

To a 50 mL BF, Diphyllin (200 mg, 5.26 mmol), 2-cyclopentyl-2-phenylacetic acid (107 mg, 5.26 mmol), DMAP (642 mg, 52.6 mmol) in 10 mL of DCM was cooled (at 0 °C). The reaction mixture was stirred for 30 min. and then DCC (119 mg, 5.78 mmol dissolved in cold DCM) was added dropwise. The reaction was stirred at RT overnight. The reaction was monitored using TLC (98:2, DCM:MeOH). After completion, the solid obtained was filtered off and the filtrate was diluted with DCM and washed with water twice. The combined organic layer was dried over Na2S04 and concentrated under reduced pressure. The obtained solid was purified by column chromatography (DCM:MeOH, 98:2).

% Purity: 99%; LC-MS (ESI) m/z: 567 [M+H] ⁺

1H-NMR (400 MHz, CDC13): δ = 7.55 - 7.53 (m, 2H), 7.42 (m, 2H), 7.35 (m, 2H), 7.05 (s, IH), 6.96 (m, IH), 6.80 (m, 2H), 6.66 (s, IH), 6.06 (d, IH, J = 1.6 Hz), 6.04 (d, IH, J = 1.2 Hz), 5.07 (s, 2H), 3.76 (s, 3H), 3.52 (s, 3H), 2.89 - 2.79 (m, IH), 2.20 - 2.14 (m, IH), 1.78 (m, IH), 1.71 (m, 4H), 1.65 (m, 4H).

EXAMPLE 5

Synthesis of compound of Formula IX (numbered as 23 in Scheme 8) Scheme 8

Reagents and conditions: a) a-phenylcyclopentaneacetic acid, DMAP (4- Dimethylaminopyridine), DCC (Ν,Ν'-Dicyclohexylcarbodiimide), DCM (Dichloromethane), 0 °C overnight.

Experimental:

Synthesis of l-(benzo[d][l,3]dioxol-5-yl)naphthalen-4-yl 2-cyclopentyl-2- phenylacetate( 23):

To a 50 mL RBF, 5 (200 mg, 7.5 mmol), l-methyl- lH-pyrrole-2-carboxylic acid (93.6 mg, 7.5 mmol), DMAP (924 mg, 75 mmol) in 10 mL of DCM was cooled (at 0 °C). The reaction mixture was stirred for 30 min. and then DCC (171.6 mg, 8.33 mmol, dissolved in cold DCM) was added dropwise. The reaction was stirred at RT overnight. The reaction was monitored using TLC (98:2, DCM:MeOH). After completion, the solid obtained was filtered off and the filtrate was diluted with DCM and washed with water twice. The combined organic layer was dried over Na ₂ S0 ₄ and concentrated under reduced pressure. The obtained solid was purified by column chromatography (DCM:MeOH, 98:2).

% Purity: 99%; LC-MS (ESI) m/z: 451 [M+H] ⁺

1H NMR (400 MHz, CDC13) 6: 7.91 - 7.83 (m, 1H), 7.53 (d, J = 7.0 Hz, 3H), 7.48 (d, J = 7.4 Hz, 1H), 7.46 - 7.38 (m, 6H), 7.33 (d, J = 7.7 Hz, 1H), 7.15 (d, J = 7.7 Hz, 1H), 6.91 (dd, J = 2.3, 6.7 Hz, 3H), 6.04 (s, 2H), 3.74 (d, J = 11.2 Hz, 1H), 2.81 (d, J = 9.4 Hz, 1H), 1.92 (d, J = 9.9 Hz, 1H), 1.81 1.65 (m, 1H), 1.63 - 1.47 (m, 1H), 1.29 (d, J = 25.2 Hz, 3H).

EXAMPLE 6

Synthesis of compound of Formula X (numbered as 24 in Scheme 9)

Synthesis l-(benzo[d][l _f 3]dioxol-5-yl)naphthalen-4-yl l-methyl-lH-pyrrole-2- carboxylate ( 24):

Scheme 9

Reagents and conditions: a) l-methyl-2-pyrrolecarboxylic acid, DMAP, DCC, DCM, 0 °C overnight.

5 24

Experimental:

Synthesis l-(benzo[d] [l,3]dio ol-5-yl)naphthalen-4-yl l-inethyl-lH-pyrrole- 2-carboxylate ( 24): To a 50 mL RBF, 5 (200 mg, 7.5 mmol), 2-cyclopentyl-2- phenylacetic acid (154.5 mg, 7.5 mmol), DMAP (924 mg, 75 mmol) in 10 mL of DCM was cooled (at 0 °C). The reaction mixture was stirred for 30 min. and then DCC (171.6 mg, 8.33 mmol, dissolved in cold DCM) was added dropwise. The reaction was stirred at RT overnight. The reaction was monitored using TLC (98:2, DCM:MeOH). After completion, the solid obtained was filtered off and the filtrate was diluted with DCM and washed with water twice. The combined organic layer was dried over Na ₂ S0 ₄ and concentrated under reduced pressure. The obtained solid was purified by column chromatography (DCM:MeOH, 98:2). 1H NMR (400 MHz, CDC ) 6: 8.08 - 8.00 (m, 1H), 7.98 - 7.90 (m, 1H), 7.55 - 7.42 (m, 2H), 7.46 - 7.37 (m, 2H), 7.35 (d, J = 7.7 Hz, 1H), 7.01 - 6.90 (m, 4H), 6.29 (dd, J = 2.5, 4.0 Hz, 1H), 6.05 (s, 2H), 4.00 (s, 3H).

% Purity: 99%; LC-MS ( 81) m/z 372 [M+H] ⁺ EXAMPLE 7

Synthesis of compound of Formula XI (numbered as 31 in Scheme 11)

Synth esis of (3S, 4R, 5R)-2- (l-(benzo[ djf 1, 3]dioxol-5-yl)naphth alen-4-yloxy)- tetrahydro-2H-pyran-3,4, 5-triol (31 ) :

Scheme 10

28 29

27

Reagents and conditions: a) Ac ₂ 0, pyridine; b) HBr ^» AcOH, DCM (Dichloromethane);

Experimental:

Synthesis of Tetra-O-acetyl-L-Arabinose (28):

To a 500-mL three-neck RBF equipped with guard-tube and stopper, were added 27 (40.0 g, 0.266 mol), pyridine (200 n L) and cooled it at 0 °C. Acetic anhydride (200 n L) was added dropwise to the above mixture at 0 °C. The resulting reaction mixture was stirred at 0 °C for 5 h. After consumption of starting materials, as judged by TLC (5:5, EtOAc: Hexane), reaction mixture was poured into ice water (500 mL) and ether was added (200 mL). Organic layer was separated and aqueous layer was extracted with ether (2 x 250 mL). Organic layers were combined and washed with saturated cupric salt solution till free from pyridine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to give sticky solid compound 28.

1H-NMR (300 MHz, CDC13): δ = 6.27 (d, 1H, J = 3.6 Hz), 5.70 (t, 1H, J = 9 Hz), 5.06 (m, 2H), 3.97 (dd, 1H, J =6.0, 1 1.1 Hz), 3.72 (t, 1H, J = 1 1.0 Hz), 2.18 (s, 3H), 2.07(s, 6H), 2.03 (s, 3H).

Synthesis of 2 Bromo 3,4, 5-Tri-O-acetyl-a-L-Arabinose (29):

1 L-RBF with guard tube was charged 28 (20.0 g, 62.9 mmol) and dichloromethane (500 mL) and mixture was cooled to 0 °C in ice bath. To the above cold solution was added hydrogen bromide (33 % in acetic acid; 46 mL) with constant stirring during lh and reaction mixture was further stirred at room temperature for lh. After completion of reaction as judged by TLC (4:6, EtOAc: Hexane), reaction mixture was washed with ice water (1 x 500 mL), 1 % NaHC0 ₃ solution (1 x 500 mL), 10 % NaHC0 ₃ solution (2 x 500 mL) and finally by brine solution (1 x 500 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtained white solid of 29.

1H-NMR (300 MHz, CDC13): δ = 6.59 (d, 1H, J= 3.9 Hz), 5.60 (t, 1H, J= 9.9 Hz), 5.05- 5.03 (m, 1H), 4.77 (dd, 1H, J= 3.9, 9.6 Hz), 4.07 (dd, 1H, J= 6.3, 11.4 Hz), 3.88 (t, 1H, J= 11.1 Hz), 2.10 (s, 3H), 2.06 (s, 6H). Scheme 11

Reagents and conditions: a) Bu ₄ NBr, 2M NaOH, DCM (Dichloromethane), RT; b) K ₂ C0 ₃ MeOH, RT.

Synthesis of (3S,4R,5R)-2-(l- enzo[d][l,3]&oxol-5-yl)naphthalen-4-yloxy)- tetrahydro-2H-pyran-3,4, 5-triacetate (30):

To a 50 mL RBF, 5 (0.4 g, 1.5 mmol), 29 (0.826 g, 3.0 mmol) and tetrabutyl ammonium bromide (0.9 g, 1.5 mmol) were taken in dichloromethane (20 mL) with stirring. To this suspension was added 2M NaOH (3 mL) solution and stirring was continued for 2 h at room temperature. After the completion of reaction as judged by TLC (4 : 6, EtOAc: Hexane), the reaction mixture was extracted with dichloromethane (4 x 20 mL). The combined organic layer washed with 10% NaOH solution (3 x 15 mL) followed by water (2 x 10 mL) and dried over anhydrous sodium sulfate. Inorganic salts were filtered off; filtrate was concentrated under reduced pressure and crude mass which was purified by column chromatography using EtOAc: Hexane (40:60) as eluent to 30 as white solid. Synth esis of (3S, 4R, 5R)-2- (l-(benzo[ d][ /, 3]dioxol-5-yl)naphth alen-4-ylox )- tetrahydro-2H-pyran-3,4, 5-triol (31 ) :

To a solution of 30 (0.416 g, 0.797 mmol) in methanol (20 mL) was added solid anhydrous K ₂ C0 ₃ (0.440 g 3.188 mmol) and reaction mixture was stirred at room temperature for 30 min. After completion of reaction as judged by TLC (5:95, MeOH : EtOAc), methanol was removed under reduced pressure, water was added and extracted with CH ₂ C1 ₂ (2 x 25 mL). Organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to get 31 as white fluffy solid.

1H-NMR (400 MHz, CDC13): δ = 8.43 (m, 1H), 7.81 (m, 1H), 7.54-7.48 (m, 2H), 7.31 (d, 1H, J = 7.6 Hz), 7.14 (d, 1H, J = 8.0 Hz), 6.94 (m, 3H), 6.03 (s, 2H), 5.37 (d, 1H, J= 5.2 Hz), 5.10 (d, 1H, J = 6 Hz), 4.89 (d, 1H, J = 5.2 Hz), 4.68 (d, 1H, J = 4.4 Hz), 3.86 (m, 3H), 3.61 (m, 2H).

EXAMPLE 8 Synthesis of compound of Formula XII (numbered as 40 in scheme 13):

Synthesis of N-(l-(benzo[d] [l,3]dioxol-5-yl)naphthalen-4-yl)furan-2- carboxamide. :

Scheme 13:

Reagents and conditions: a) NBS, DCM, 0°C, lhr; b) Tetrakis palladium (0), Na ₂ C0 ₃ , H ₂ 0, DME (Dimethoxyethane), reflux, 12 hrs; c) furan-2-carbonyl chloride, Triethylamine, DCM, rt, 12 hrs

Synthesis of 4-bromonaphthalen-l-amine (38):

Single neck BF (500 mL) equipped with magnetic stirrer and guard tube was charged with naphthylamine (37, 10 g, 0.069 mol) and DCM (300 mL). To this solution was added N-Bromosuccinimide (12.43 gm, 0.0698 mol) portionwise with constant stirring over half an hour at 0°C. and stirring was further continued for 1 h at room temperature. During this time all the starting materials was consumed as confirmed by TLC (3:7, EtOAc: Hexane). Reaction mixture was added in cold water (150 mL). The reaction mixture was extracted with dichloromethane (3 x 200 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (5- 20%) in hexane as eluent to afford 38 as a white solid (Yield = 3.5 gm).

Synthesis of 4-(benzo[d][l,3]dioxol-5-yl)naphthalen-l-amine (39): Single necked BF (250 mL) equipped with magnetic stirrer, condenser and guard tube was charged with 4-bromonaphthalen-l -amine (38, 0.5g, 2.90 mmol) and 3, 4 (methylenedioxy) phenylboronic acid (0.578 gm, 3.48 mmol) in DME (7 mL). To this solution was added sodium carbonate (0.615 gm, 5.80 mmol) dissolved in water (2.5 mL). Reaction mixture was stirred at rt for 10 minutes and then added tetrakis palladium (0) (0.168 gm, 0.145 mmol). Reaction mixture was refluxed for 12 hrs. During this time all the starting materials was consumed as confirmed by TLC (2:8, EtOAc: Hexane). Reaction mixture was added in water (100 mL). The reaction mixture was extracted with ethyl acetate (3 x 100 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (5- 20%) in hexane as eluent to afford 39 as a white solid (Yield = 0.5 gm).

Synthesis of N-(l-(benzo[d] [l,3]dioxol-5-yl)naphthalen-4-yl)furan-2- carboxamide (40):

Single neck RBF (500 mL) equipped with magnetic stirrer and guard tube was charged with 4-(benzo[d] [l,3]dioxol-5-yl)naphthalen-l-amine (39, 0.2 g, 0.76 mmol), trimethylamine (0.22 mL, 1.52 mmol) and DCM (10 mL). To this solution was added furan-2-carbonyl chloride (0.11 mL, 1.14 mmol) dropwise with constant stirring over half an hour at 0°C. and stirring was further continued for 12 h at room temperature. During this time all the starting materials was consumed as confirmed by TLC (3:7, EtOAc: Hexane). Reaction mixture was added in cold water (100 mL). The reaction mixture was extracted with dichloromethane (2 x 100 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (10- 30%) in hexane as eluent to afford 40 as a white solid (Yield = 0.1 gm). 1H-NMR (400 MHz, DMSO): δ = 8.54 (s, 1H), 8.13 (d, 1H, J= 7.6 Hz), 7.98 (t, 2H, J= 8.8 Hz), 7.61 (m, 2H), 7.50 (m, 2H), 7.26 (s, 1H), 6.96 (m, 3H), 6.63 (m, 1H), 6.05 (s, 2H).

EXAMPLE 9

Synthesis of compound of Formula XIII (numbered as 36 in scheme 12) Synthesis of 5-(benzo[d] [l,3]dioxol-5-yl)-8-(benzyloxy)quinoIine

hydrochloride :

Scheme 12:

Reagents and conditions: a) K ₂ C0 ₃ , DMF (Dimethylformamide), RT, 16 hrs; b) NBS, DCM, 0°C, lhr; c) Tetrakis palladium (0), Na ₂ C0 ₃ , H ₂ 0, DME (Dimethoxyethane), reflux, 12 hrs; d) MeOH.HCl, RT, 2 hrs

Experimental:

Synthesis of 8-(ben yloxy)quinoline (33):

Three necked RBF (500 mL) equipped with dropping funnel, magnetic stirrer, and guard tube was charged with 8-Hydroxyquinolin (32, 5 g, 0.0344 mol), potassium carbonate (9.5 gm, 0.0688 mol) and DMF (100 mL). To this solution was added benzylbromide (6.13 mL, 0.0516 mol) dropwise with constant stirring over half an hour and stirring was further continued for 12 h at room temperature. During this time all the starting materials was consumed as confirmed by TLC (3:9, EtOAc: Hexane). Reaction mixture was added in cold water (250 mL). The reaction mixture was extracted with ethyl acetate (3 x 100 mL). All the organic layer combine and washed with water (3 x 100 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (5- 10%) in hexane as eluent to afford 33 as a white solid (Yield = 5.2 gm).

Synthesis of 8-(benzyloxy)-5-bromoquinoline (34):

Single necked RBF (250 mL) equipped with magnetic stirrer, and guard tube was charged with 8 -benzyl oxyquinolin (33, 4 g, 0.016 mol) in DCM (100 mL). To this solution was added N-Bromosuccinimide (3.02 gm, 0.016 mol) portiowise with constant stirring over half an hour at 10°C and stirring was further continued for 1 h at room temperature. During this time all the starting materials was consumed as confirmed by TLC (2:8, EtOAc: Hexane). Reaction mixture was added in cold water (150 mL). The reaction mixture was extracted with dichloromethane (3 x 100 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (5- 10%) in hexane as eluent to afford 34 as a white solid (Yield = 3.9 gm).

Synthesis of 5-(benzo[d][l,3]dioxol-5-yl)-8-(benzyloxy)quinoline (35):

Single necked RBF (250 mL) equipped with magnetic stirrer, condenser and guard tube was charged with 8-(benzyloxy)-5-bromoquinoline (34, 1 g, 0.00318 mol) and 3, 4 (methylenedioxy) phenylboronic acid (0.79 gm, 0.00477 mol) in DME (20 mL). To this solution was added sodium carbonate (0.673 gm, 0.00636 mol) dissolved in water (3.2 mL). Reaction mixture was stirred at rt for 10 minutes and then added tetrakis palladium (0) (0.183 gm, 0.000159 mol). Reaction mixture was refluxed for 12 hrs. During this time all the starting materials was consumed as confirmed by TLC (3:7, EtOAc: Hexane). Reaction mixture was added in water (100 mL). The reaction mixture was extracted with ethyl acetate (3 x 100 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (10- 20%) in hexane as eluent to afford 35 as a white solid (Yield = 0.94 gm).

Synthesis of 5-(beiizo[d][l,3]dioxol-5-yl)-8-(benzyloxy)quinoIiiie

hydrochloride (36):

Single necked RBF (250 mL) equipped with magnetic stirrer and guard tube was charged with 5-(benzo[d][l,3]dioxol-5-yl)-8-(benzyloxy)quinoline (35, 0.2g) in dry DCM (10 mL). To this solution was added methanolic HC1 at 0°C. Reaction mixture was stirred for 2 hrs at 0°C. Reaction mixture was monitored with TLC. The reaction mixture was concentrated under reduced pressure. The crude compound was crystalized using ethyl acetate and pet ether to afford 36 as a white solid (Yield = 0.1 gm).

1H-NMR (400 MHz, DMSO): 5 = 9.1 1 (d, 1H, J= 4.4 Hz), 8.74 (d, 1H, J= 8.4 Hz), 7.93 (m, 1H), 7.63 (m, 4H), 7.41 (m, 3H), 7.14 (m, 2H), 7.06 (m, 1H), 6.12 (s, 2H), 5.51 (s, 2H).

EXAMPLE 10

Synthesis of compound of Formula XIV (numbered as 41 in scheme 14): Synthesis of 4-phenyIiiaphthalen- N,N-Di-methylsulphonainide. :

Scheme 14:

Reagents and conditions: a) Triethylamine, DCM, 0°C, lhr, RT for 2 hr

Experimental

Synthesis of 4-phenyInaphthalen- N,N-Di-methylsulphonamide. (Comp. 41):

Single neck RBF (100 mL) equipped with magnetic stirrer and guard tube was charged with 4-phenylnaphthalen- 1 -amine (39, 0.1 g, 0.45 mmol), trimethylamine (0.5 mL, 0.90 mmol) and DCM (10 mL). To this solution was added methane sulphonyl chloride (0.5 mL, 0.67 mmol) dropwise with constant stirring over half an hour at 0°C. and stirring was further continued for 2 h at room temperature. During this time all the starting materials was consumed as confirmed by TLC (1:9, EtOAc: Hexane). Reaction mixture was added in cold water (100 mL). The reaction mixture was extracted with dichloromethane (2 x 100 mL). Organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude mass was purified by column chromatography over silica gel using ethyl acetate (5- 20%) in hexane as eluent to afford 41 as a white solid (Yield = 0.15 gm).

1H-NMR (400 MHz, DMSO): δ = 8.15 (d, 1H, J= 8.4 Hz), 7.94 (d, 1H, J= 8.4 Hz), 7.68 (m, 1H), 7.60 (m, 1H), 7.51 (m, 7H), 3.56 (s, 6H). Example 11

Cancer Cell assays

In vitro Antiproliferative Assay (MTT Assay)

MTT assay is a simple and sensitive assay where, metabolic reducing activity of the cells is measured. The increase of this activity in time is taken as a parameter of cell growth. If treatment with a drug impairs this increase, the action may be a consequence of growth inhibition, cell killing or both. The compounds of Formula V to XIV of the present invention, standard cytotoxic drug (e.g. Cisplatin) were tested at different concentrations (l,0.1,0.01,0.001mM) using breast and prostate cancer cell lines. All cell lines were cultured in a 37°C incubator with a 5% C0 ₂ environment. Compounds were dissolved in DMSO with a concentration of 0.1M (stock solution). Cells were seeded into 96-well plates at suitable plating efficiency.

Following plating efficiencies were standardized for MTT assay:

Table 1 Plating efficiency (No. of

Cell lines Name of the cell line

cells/well or per 200μ1)

MCF7 7500

Breast

MDAMB231 10000

PC3 10000

Prostate

DU145 5000

The MTT procedure followed was as follows. Briefly, the cells were plated in 96 well plate as per predetermined plating efficiency(Tablel) The plates were then incubated for 24 hrs in 5% C0 ₂ atmosphere at 37°C. Appropriate concentrations of the drugs were then added to the plate and further incubation was carried out for 48 hrs (in 5% C0 ₂ atmosphere at 37 °C). The assay plate was then centrifuged twice at 3000 rpm for 3 mins and supernatant was then discarded. 100 ul of MTT solution (0.5 mg/ml) was then added to each well of the plate and it was further incubated for 4hrs (in 5% C0 ₂ atmosphere at 37 °C.) Following 4 hr incubation, the plate was then centrifuged twice, and supernatant was aspirated off very carefully. 200 ul of DMSO was then added to each well to solublize. MTT crystals and mixed well by shaking the plate. XY graph of log Percent viability was then plotted against log drug concentration. IC50 (Drug concentration inhibiting the 50 % of cell population) was then calculated by regression analysis. Soft Agar Assay

The Soft Agar Colony-formation Assay is an anchorage-independent growth assay in soft agar, which is one of the most stringent assays for detecting malignant transformation of cells. For this assay, malignant cells are cultured with appropriate controls in soft agar medium for 1-2 weeks. Following this incubation period, formed colonies can either be analyzed morphologically using cell stain and quantifying the number of colonies formed. The results of the assay are comparable to those obtained after injecting tumorigenic cells into nude mice and is regarded as the "gold standard" for testing the tumorigenicity of cells in vitro (one of the important features of cancer stem cells, CSCs).

Briefly, for Soft Agar Assay a mixture of 50 ul of 2X medium (taken appropriately as per cell line) and 50 ul of 1.2% Bacto Agar were plated on to each well of 96 well micro titer assay plate. 10 ul of cells (Of specific plating efficiency pre- standardized for respective cell line) were mixed with 20 ul of 2X medium and 30 ul of 0.8 % of Bacto Agar and 1.6 ul of drug (of appropriate concentration) in a vial and transferred to the solidified pre-layers of the assay plates. The cells were then allowed to grow and form colonies at 37 °C. and 5% C02 for 1 week. An intermittent feeding with 50 ul of appropriate 2X medium was performed after 3 days of experimental set up. l6ul of Alamar Blue (1.5 mg/ml) was then added to all the wells to quantify the developed colonies. The plates were incubated for 24hrs at 37 °C. Absorbance was then measured at 630nm. XY graph of log Percent viability was then plotted against log drug concentration. IC50 (Drug concentration inhibiting the 50 % of cell population) was then calculated by regression analysis.

Following plating efficiencies were standardized for Soft Agar Assay: Table 2 Stem cell assays:

In Vitro Sphere-forming Assay: Sphere assay measures the ability of Cancer Stem Cellss to form spheres in specially designed serum-free medium. We have used this assay to measure the killing efficiency of the test compounds as compared to the standard chemotherapeutic drug, Cisplatin.

Materials and Reagents :50X B27 Supplement (Life Technologies, Invitrogen, Catlog No.: 17502-044),Fibroblast Growth Factor (FGF) (Sigma- Aldrich, Catlog No. : F029125),Epidermal Growth Factor (EGF) (Sigma- Aldrich, Catlog No.: E9644), Insulin (Sigma, Catlog No.: 19278), Dulbecco's Modified Eagle Medium/F12 (HiMedia Catlog No. : AL139-6), Dulbecco's Phosphate Buffered Saline (HiMedia Catlog No. : TL1006),Trypan Blue (TCI 93), Prostate Epithelial Media (LONZA, Catlog No. : CC-3166) MEGM (LONZA, Catlog No. : CC- 3051),Heparin (Sigma, Catlog No.: H3393),Penstrep (HiMedia, Catlog No.: A002) Mammosphere Media Preparation (For 100 mL): 1 g methyl cellulose autoclaved with magnetic stirrer Plain media (MEBM), 100 mL added and dissolved under magnetic stirring. After complete dissolution, add: FGF- 80 Ε, EGF- 40 μί, Penstrep- 1 mL, Heparin- 400 μL.

Prostosphere Media Preparation (For 100 mL): l g methyl cellulose autoclaved with magnetic stirrer, Plain media (Prostate Epithelial Basal Medium), 100 mL added and dissolved, under magnetic stirring. After complete dissolution, add: Insulin- 40 μί, B27- 2 mL, EGF- 80 μΐ,, Penstrep- 1 ml. Procedure: -The cells were trypsinised and made into single-cell suspension by passing through cell strainers (100 μΐ and 40 μΐ, respectively), The cells were diluted at the concentration of 2000 cells/ 100 μΐ. and suspended in either Mammosphere (for breast cell lines) or Prostosphere (for prostate cell lines). 100 μΐ _^ of this suspension was added into each well of 96-well suspension plates and incubated at 37 °C, 5% C0 ₂ for 24 hrs. Appropriate concentrations of the drugs (2 μΐ.) were added into respective wells with 100 μΐ _^ of stem cell culture medium. Plates were incubated at 37 °C, 5% C0 ₂ for 72 hrs. After incubation 2.5 μL· of the respective drug concentration and 50 μΐ _^ of stem cell culture medium were added into each well and the plates were further incubated at 37 °C, 5% C0 ₂ for 72 hrs. 3 μΐ _^ of the respective drug concentration was added with 50 μΐ _^ of stem cell culture medium again after incubation and plates were incubated again for 72 hrs at 37 °C, 5% C0 ₂ .Number of primary spheres formed for each concentration was counted. A comparative graph of number of spheres formed was plotted against the concentration and the growth curve was compared with the positive control.

Normal Cell assays:

It is very important that the sensitivity of a cytotoxic drug towards malignant and normal cells is different. In the first place, the clinical use of drugs with a preferential toxicity towards malignant cells is preferred.

In order to test the activity of cytotoxic drugs towards normal cells, we performed MTT Assay for these cytotoxic drugs using lymphocytes obtained from a healthy donor.

Human lymphocytes can be readily isolated from peripheral blood, centrifuged at low speeds for 3 Omins. Briefly, diluted defibrinated fresh blood was overlaid gradually on HiSeP LSM1077 and centrifuged at low speed for 30mins. The lymphocyte layer (the buffy coat) (Fig)was carefully removed in a new collection tube. The buffy coat was given another wash, by the diluent buffer, to reduce the platelet contamination. The supernatant was discarded, and the pellet was resuspended in diluent buffer. The viability was checked by Haemocytometer. Cells with Viability and Purity of 95% and more were considered for the assay.MTT assay was performed with these cells as described above with plating efficiency of 0.7million/ml.

EXAMPLE 12

Results of activity of Formula V Table 3: MTT Results of Formula V for Breast Cell lines IC50 in micromolar

Table 3 indicates that activity of Formula V on breast cancer cell line is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 4: MTT Results of FORMULA V for Prostate Cell lines IC50 in micromolar Sr. No Cell line Cisplatin Formula V

1 PC3 27.99 6.19

The results indicate that activity of Formula V on prostate cancer cell line is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 5: Soft Agar Assay Results of Formula V for Breast Cell lines IC50 in micromolar

Table 5 indicates the anticancer activity exhibited by Formula V is on breast cancer cell line MDAMB231 is higher than standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 6: Soft Agar Assay Results of Formula V for Prostate Cell lines IC50 in micromolar

Table 6 indicates the anticancer activity of Formula V is higher on prostate cancer cell line in soft Agar Assay

Table 7: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 7 indicates Formula V is effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisp latin.

Table 8: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 8 indicates that Formula V is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin.

EXAMPLE 13

Results of Activity of Formula VI

Table 9: MTT Results of Formula VI for Breast Cell lines IC50 in micromolar

Table 9 indicates that activity of Formula VI on breast cancer cell line is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 10: MTT Results of Formula VI for Prostate Cell lines IC50 in micromolar Table 10. indicates that activity of FORMULA VI on Prostrate cancer cell line is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Results of MTT assay indicates that compound of Formula VI exhibits higher anticancer activity on breast and prostate Cancer cell lines compared to standard chemo therapeutic drug Cisplatin.

Table 11: Soft Agar Assay Results of Formula VI for Breast Cell lines IC50 in micromolar

Table 11 indicates the anticancer activity of Formula VI is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 12: Soft Agar Assay Results of Formula VI for Prostate Cell lines IC50 in micromolar

Table 12 indicates the anticancer activity of Formula VI is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay The results Indicates that Formula VI exhibits higher anticancer activity on breast and prostate Cancer cell lines compared to standard chemotherapeutic drug Cisplatin in Soft Agar Assay.

Table 13: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 13 indicates that Formula VI is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin.

Table 14: 3D sphere count of PC3 in Prostosphere media at plating efficiency of

2000 cells/well (n=6±S.D)

Table 14 indicates that Formula VI is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin.

EXAMPLE 14 Results of Activity of Formula VII

Tablel5: MTT Results of Formula VII for Breast Cancer Cell lines IC50 in micromolar

Table 15 indicates that activity of Formula VII on breast cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Tablel6: MTT Results Formula VII for Prostate Cancer Cell lines IC50 micromolar

Table 16 indicates that activity of Formula VII on prostate cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 17: Soft Agar Assay Results of Formula VII for Breast Cell lines IC50 in micromolar Sr. No Cell line Cisplatin Formula VII

1. MDAMB231 24.79 7.91

Table 17 inc icates the anticancer activity of FORMULA VI is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 18: Soft Agar Assay Results of Formula VII for Prostate Cell lines IC50 in micromolar

Table 18 results indicate the anticancer activity of Formula VII is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

In Vitro Sphere-forming Assay Table 19: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 19 indicates the that Formula VII is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin.

Table 20: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 20 indicates that Formula VII is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin. EXAMPLE 15

Results of Activity Formula VIII

Table 21: MTT Results of Formula VIII for Breast Cell lines IC50 in micromolar

Table 21 indicates that activity of FORMULA VIII on breast cancer cell lines is higher compared to standard therapeutic drug Cisplatin in MTT assay.

Table 22: MTT Results of Formula VIII for Prostate Cell lines IC50 in micromolar Sr. No Cell line Cisplatin Formula VIII

1 PC3 29.02 3.91

2. DU145 23.86 4.28

Table 22 indicates that activity of Formula VIII on prostate cancer cell lines is higher compared to standard therapeutic drug Cisplatin in MTT assay.

Table 23: Soft Agar Assay Results of Formula VIII for Breast Cell lines IC50 in micromolar

Table 23 indicates the anticancer activity of Formula VIII is higher on breast cancer cell line MDAMB231 compared to standard therapeutic drug Cisplatin in soft Agar Assay.

Table 24: Soft Agar Assay Results of Formula VIII for Prostate Cell lines IC50 in micromolar

Table 24 indicates the anticancer activity of Formula VIII is higher on prostate cancer cell line PC3 compared to standard therapeutic drug Cisplatin in soft Agar Assay .

Table 25 : 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D) Drug GC GCD(Growth Cone in 250 25 2.5 0.25 0.025 (Growth Control With uM Control) DMSO)

Cisplatin 23(±5) 38(±8) 51(±5) 69(±7) 89(±4) 86(±6) 78(±2)

Formula

0(±0) 8(±2) 13(±2) 29(±4) 36(±3) 86(±6) 78(±2) VIII

Table 25 indicates the that Formula VIII is more effective on spheres of MDAMB231 compared to standard therapeutic drug Cisplatin

Table 26: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 26 indicates that Formula VIII is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin

EXAMPLE 16

Results of Activity of Formula IX

Table 27: MTT Results of Formula ΓΧ for Breast Cell lines IC50 in micromolar

Table 27 indicates that activity of FORMULA IX on breast cancer cell lines higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 28: MTT Results of Formula IX for Prostate Cell lines IC50 micromolar

Table 28 indicates that activity of Formula IX on prostate cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 29: Soft Agar Assay Results of Formula IX for Breast Cell lines IC50 in micromolar

Table 29 indicates the anticancer activity of Formula IX is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 30: Soft Agar Assay Results of Formula IX for Prostate Cell lines IC50 in micromolar Table 30 indicates the anticancer activity of Formula ΓΧ is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 31 : 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 31 indicates that Formula IX is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin.

Table 32: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 32 indicates that Formula IX is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin.

EXAMPLE 17 Results of Activity of FORMULA X

Table 33: MTT Results of Formula X for Breast Cell lines IC50 in micromolar

Table 33 indicates that activity of Formula X on breast cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 34: MTT Results of Formula X for Prostate Cell lines IC50 in micromolar

Table 34 indicates that activity of Formula X on prostate cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 35: Soft Agar Assay Results of Formula X for Breast Cell lines IC50 in micromolar

Table 35 indicates the anticancer activity of Formula X is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 36: Soft Agar Assay Results of Formula X for Prostate Cell lines IC50 in micromolar

Table 36 indicates the anticancer activity of Formula X is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

In Vitro Sphere-forming Assay Table 37: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 37 indicates that Formula X is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin. EXAMPLE 18 Results of Activity of Formula XI

Table 38: MTT Results of Formula XI for Breast Cell lines IC50 in micromolar

Table 38 indicates that activity of ormula XI on breast cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT

Table 39: MTT Results of Formula XI for Prostate Cell lines IC50 in micromolar

Table 39 indicates that activity of FORMULA XI on prostate cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 40: Soft Agar Assay Results of Formula XI for Breast Cell lines IC50 in micromolar Table 40 indicates the anticancer activity of Formula XI is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 41: Soft Agar Assay Results of Formula XI for Prostate Cell lines IC50 in micromolar

Table 41 indicates the anticancer activity of Formula XI is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

EXAMPLE 19

Results of Activity of Formula XII

Table 42: MTT Results of Formula XII for Breast Cell lines IC50 in micromolar

Table 42 indicates that activity of Formula XII on breast cancer cell lines higher compared to standard chemotherapeutic drug Cisplatin in MTT assay. Table 43: MTT Results of Formula XII for Prostate Cell lines IC50 in micromolar

Table 43 indicates that activity of Formula XII on prostate cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay. Table 44: Soft Agar Assay Results of Formula XII for Breast Cell lines IC50 in micromolar

Table 44 indicates the anticancer activity of Formula XII is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 45: Soft Agar Assay Results of Formula XII for Prostate Cell lines IC50 in micromolar Table 45 indicates the anticancer activity of Formula XII is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

In Vitro Sphere-forming Assay Table 46: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 46 indicates that Formula XII is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin.

Table 47: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 47 indicates that Formula XII is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin.

EXAMPLE 20 Results of Activity of Formula XIII

Table 48: MTT Results Formula XIII for Breast Cell lines IC50 in micromolar

able 48 indicates that activity of Formula XIII on breast cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 49: MTT Results of Formula XIII for Prostate Cell lines IC50 in micromolar

Table 49 indicates that activity of Formula XIII on prostate cancer cell lines is higher compared to standard chemotherapeutic drug Cisplatin in MTT assay.

Table 50: Soft Agar Assay Results of Formula XIII for Breast Cell lines IC50 in micromolar

Table 50 indicates the anticancer activity of Formula XIII is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay. Table 51: Soft Agar Assay Results of Formula XIII for Prostate Cell lines IC50 in micromolar

Table 51 indicates the anticancer activity of Formula XIII is higher on prostate cancer cell line PC3 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

In Vitro Sphere-forming Assay

Table 52: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 52 indicates that Formula XIII is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin.

Table 53: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

FORMULA 0(±0) 14(± 1) 27(±3) 39(±5) 41 (±7) 80(±5) 76(±4)

XIII

Table 53 indicates that Formula XIII is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin.

EXAMPLE 21

Results of Activity of Formula XIV Table 54: Soft Agar Assay Results of Formula XIV on Breast Cell lines IC50 in micromolar

Table 54 indicates the anticancer activity of Formula XIV is higher on breast cancer cell line MDAMB231 compared to standard chemotherapeutic drug Cisplatin in soft Agar Assay.

Table 55: 3D sphere count of MDAMB231 in Mammosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 55. indicates that Formula XIV is more effective on spheres of MDAMB231 compared to standard chemotherapeutic drug Cisplatin. Table 56: 3D sphere count of PC3 in Prostosphere media at plating efficiency of 2000 cells/well (n=6±S.D)

Table 56 indicates that Formula XIV is more effective on spheres of PC3 compared to standard chemotherapeutic drug Cisplatin.