Background of the Invention

The present invention relates to nitrile deπvatives and to pharmaceutical compositions comprising nitrile deπvatives The invention also relates to the pharmaceutically acceptable salts of such compounds, processes for the preparation of such compounds, intermediates used in the preparation of such compounds, and the uses of such compounds in treating hyperproliferative diseases, inflammatory diseases and viral and bacterial infections

The aforementioned derivatives and their pharmaceutically acceptable salts have one or more of the following properties AKT inhibition, inhibition of cell cycle hyperproliferation, cell cycle specific induction of apoptosis in cancer cells, inhibition of LTB ₄ activities, and antiangiogenic activities showing significant reduction in tumor size in experimental animals. These compounds are, therefore, useful in the treatment of a wide range of disorders in mammals, including, but not limited to hyperproliferative diseases, such as head and neck cancer, including gliomas, drug resistant lung cancer, estrogen dependent or non- dependent cancers in humans, non-small cell lung cancer and colon cancer Non-limiting examples of estrogen dependent cancers are breast cancer and ovarian cancer. As a result of their inhibition of LTB ₄ activities, these compounds are useful in treating inflammatory diseases such as allergy, asthma and arthritis, and as a result of their AKT inhibition and cytokine activation, these compounds are also useful in treating viral and bacterial infections. There is currently great interest in finding new therapies for the foregoing diseases.

Salts of substituted isothiourea compounds are referred to in Miller et al JACS, VoI 62, 2099 - 2103 (1940), Shapira, et al , Radiation Research, VoI 7, No. 1 , 22-34 (1957), King et al Biochemistry, VoI 17, No 8, 1499 - 1506 (1978); Bauer and Welsh, J. Org. Chem VoI 26, No. 5, 1443-1445 (1961), Southan, et al , Br J Pharmacol ,VoI 114, 510-516 (1995), and Gerber, et al., Organic Synthesis, VoI 77, 186 (2000).

Summary of the Invention

In a particular embodiment the present invention relates to a pharmaceutical composition for treating hyperproliferative diseases, including but not limited to cancer, inflammatory diseases and viral and bacterial infections in mammals, including, but not limited to, humans, comprising an antihyperproliferative disease, anti-inflammatory, antiviral or antibacterial effective amount of a compound of formula I

N-R ¹ / NC-(CH ₂ ) _n -W-(CH ₂ ) _m -Z -C

\

N-R ² I

I

R ³ wherein Z is selected from sulphur, copper, silver, gold and platinum, or Z is a halogen-containing moiety selected from CIO ₂ , BrO ₂ , and 1O ₂ wherein n is zero or an integer from 1 to 8 and m is zero or an integer from 1 to 8, R ¹ , R ² and R ³ are independently selected from hydrogen, -CH ₂ -cyclohexyl, Ci-C ₆ alkyl, C ₂ -C ₆ alkenyl, and C ₂ -C ₆ alkynyl wherein the alkyl moieties of said alkyl, alkenyl and alkynyl groups may be linear, branched and cyclic and combinations of linear, branched and cyclic alkyl, alkenyl and alkynyl moieties and said groups may be substituted with groups selected from methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl, methoxy, ethoxy, O-n-propyl, O-isopropyl, O-n-butyl, and O-t-butyl; or

R ¹ and R ² , taken together with the nitrogens to which they are directly attached and the carbon which is attached to the nitrogens, form a five or more membered ring, wherein p is an integer from 1 to 7 as shown below

N

// \ NC-(CH ₂ ) _n -W-(CH ₂ ) _m -Z -C CH ₂

I I

N — (CH ₂ )p /

R ³ wherein the broken line represents an optional double bond, with the proviso that when there is such a double bond, R ³ is absent and the CH ₂ group adjacent to the double bond has one hydrogen rather than two hydrogens, or R ² and R ³ taken together with the nitrogen to which they are attached form a three or more membered ring, wherein p is an integer from 1 to 7, as shown below

NR ¹ /

NC-(CH ₂ ) _n -W-(CH ₂ ) _m -Z -C I

N

W is absent or W is selected from -CH ₂ -, -CH ₂ -CH ₂ -, trans -CH=CH-, cis -CH=CH-, -C ≡≡≡ C-, or -CHR ⁴ -CHR ⁵ -, trans -C R ⁴ =C R ⁵ -, cis -CR ⁴ =CR ⁵ -, wherein R ⁴ , and R ⁵ are independently selected from -CH ₂ -cyclohexyl, C ₁ -C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ alkynyl, and Ci-C ₆ alkyl ether (also referred to as C ₁ -C ₆ alkyl -O- ) ; or W is a disubstituted moiety, wherein the term disubstituted is used to indicate how W is attached to the groups (CH ₂ ) _m and (CH ₂ ) _n , selected from the group of disubstituted moieties consisting of (a) a 1 ,2-, 1 ,3-, or 1 ,4-dιsubstιtuted six membered ring which may be saturated or unsaturated with one, two or three double bonds; a 1 ,2-, or 1 ,3-disubstituted five membered ring which may be saturated or unsaturated with one or two double bonds; a 1 ,2-, or 1 ,3-disubstituted four membered ring which may be saturated or unsaturated with one or two double bonds; or a 1 ,2- disubstituted three membered ring which may be saturated and unsaturated with a double bond as shown by the following formulas, wherein the substituents on said disubstituted rings are the groups attached to W in formula I

wherein the broken lines indicate optional double bonds,

(b) a 1 2-, 1 ,3-, or 1 ,4-disubstιtuted six membered ring which may be saturated or unsaturated with one, two or three double bonds, a 1 ,2-, or 1 ,3-dιsubstιtuted five membered ring which may be saturated or unsaturated with one or two double bonds, a 1 ,2-, or 1 ,3-dιsubstιtuted four membered ring which may be saturated or unsaturated with one or two double bonds, or a 1 ,2- disubstituted three membered ring which may be saturated and unsaturated with a double bond as shown by the following formulas, wherein the substituents on said disubstituted rings are the groups attached to W in formula I, and said disubstituted rings may have additional substituents R ⁶ , R ⁷ , R ⁸ , and R ⁹ as shown in the following formulas

wherein the broken lines indicate optional double bonds, wherein R ⁶ R ⁷ , R ⁸ and R ⁹ are independently selected from hydrogen, -CH ₂ -cyclohexyl, Ci-C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ alkynyl, or Ci-C ₆ alkyl ether the six membered ring may be saturated or have one, two or three double bonds, the five and four membered rings may be saturated or have one or two double bonds and the three membered ring may be saturated or have one double bond, wherein Y is nitrogen, oxygen, or sulphur,

(c) a ring selected from 1 ,2-, 1 ,3-, 1 ,4- 1 ,5-, 1 ,6-, or 1 ,7- disubstituted saturated and unsaturated nine membered rings with one or more double bonds, with ring positions numbered as shown in the first ring set forth below, said ring selected from the second to the thirteenth rings set forth below, wherein the substituents on said disubstituted rings are the groups attached to W in formula I, and said disubstituted rings may have additional substituents R ₁ R ₁ R ₁ R and R as shown in the following formulas

wherein the broken lines indicate optional double bonds; wherein R ⁶ , R ⁷ , R ⁸ , R ⁹ , and R ¹⁰ are independently selected from hydrogen, -CH ₂ -cyclohexyl, Ci-C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ alkynyl, or C ₁ -C ₆ alkyl ether; wherein Y is nitrogen, oxygen, or sulphur;

(d) a ring selected from 1 ,2-, 1 ,3-, 1 ,4-, 1 ,5-, 1 ,6-, 1 ,7-, or 1 ,8- disubstituted saturated and unsaturated naphthalene rings with one or more double bonds, with ring positions numbered as shown in the first ring set forth below, said rings selected from the second to sixth rings set forth below, wherein the substituents on said disubstituted rings are the groups attached to W in formula I, and said disubstituted rings may have additional substituents R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ and R ¹¹ as shown in the following formulas

wherein the broken lines indicate optional double bonds, wherein R ^β , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ and R ¹¹ are independently selected from hydrogen, -CH ₂ -cyclohexyl, C ₁ -C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ alkynyl, or C ₁ -C ₆ alkyl ether, wherein Y is nitrogen, oxygen, or sulphur, and

(e) a ring selected from 1 ,2-, 1 ,3-, 1 ,4-, 1 ,5-, 1 ,6-, 1 ,7- 1 ,8-, 1 ,9-, 1 ,10-, 2,5-, 3 5-, 4,5- or 5,10- disubstituted saturated and unsaturated anthracene rings with one or more double bonds, with ring positions numbered as shown in the first ring set forth below, said ring selected from the second to ninth rings set forth below, wherein the substituents on said disubstituted rings are the groups attached to W in formula I, and said disubstituted rings may have additional substituents R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ , R ¹¹ , R ¹² and R ¹³ as shown in the following formulas

wherein the broken lines indicate optional double bonds, wherein R ⁶ , R ⁷ , R ³ , R ⁹ , R ¹⁰ , R ¹¹ , R ¹² , and R ¹³ are independently selected from hydrogen, -CH ₂ -cyclohexyl, C ₁ -C ₆ alkyl, C ₂ -C ₅ alkenyl, C ₂ -C ₆ alkynyl, or C ₁ -C ₆ alkyl ether, wherein Y is nitrogen, oxygen, or sulphur, or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier

In one embodiment R ¹ R ² and R ³ are independently selected from hydrogen methyl ethyl, n-propyl, isopropyl, cyclopropyl, -CH ₂ -cyclopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, cyclobutyl, -CH ₂ -cyclobutyl, n-pentyl, sec-pentyl, isopentyl, tert-pentyl, cyclopentyl, -CH ₂ -cyclopentyl, n-hexyl, sec-hexyl, cyclohexyl, -CH ₂ -cyclohexyl, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, ethynyl, 2-propynyl (propargyl), and 1-propynyl, which may bear one or more substituents selected from methyl, ethyl, propyl, isopropyl, n- butyl, t-butyl, methoxy, ethoxy, O-n-propyl, 0-ιsopropyl, O-n-butyl, and O-t-butyl

In a one embodiment of the invention, the compound of formula I is a compound of formula Il

N-R ¹ X

NC-(CH ₂ ) _n -W-(CH ₂ ) _m -Z -C - N-R ² I

R

wherein π, m, W, Z, R ¹ , R ² , and R ³ are as defined above and X is a pharmaceutically acceptable acid In one embodiment the acid is HCI In another embodiment the acid is HBr In one embodiment of the invention, Z is sulfur, copper, silver, gold or platinum In another embodiment of the invention, Z is sulfur In another embodiment of the invention, Z is copper In another embodiment of the invention, Z is gold In another embodiment of the invention, Z is a halogen-containing moiety as defined above In another embodiment of the invention, R ¹ , R ² and R ³ are each hydrogen In one specific compound of the invention, Z is copper, R ¹ , R ² and R ³ are each hydrogen, m is 1 n is 1 and W iS CH ₂

In one embodiment of the invention, R ⁴ , R ⁵ , R ^s , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ , R ¹¹ , R ¹² , and R ¹³ are independently selected from hydrogen, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, -CH ₂ -cyclopropyl, vinyl, allyl, n- butyl, sec butyl, isobutyl, tert-butyl, cyclobutyl, -CH ₂ -cyclobutyl, n-pentyl, sec-pentyl, isopentyl, tert-pentyl, cyclopentyl, -CH ₂ -cyclopentyl n-hexyl, sec-hexyl, cyclohexyl, -CH ₂ -cyclohexyl, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, ethynyl, 2-propynyl (propargyl), and 1-propynyl, which may bear one or more substituents selected from methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl, methoxy, ethoxy, O-n-propyl, 0-ιsopropyl, O-n-butyl, and O-t-butyl

In one embodiment of the invention W is allyl or vinyl One embodiment of the present invention relates to a pharmaceutical composition for the treatment of hyperprohferative diseases, including but not limited to cancer, inflammatory diseases, and viral and bacterial infections in mammals comprising an antihyperprohferative disease, antiinflammatory, antiviral or antibacterial effective amount of 4-ιsothιoureιdobutyronιtrιle (also named S-(3-cyanopropyl)ιsothιourea or S-(γ-cyanopropyl)lιsothιourea) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier In a particular embodiment, the composition comprises the hydrochloride acid addition salt of 4-ιsothιoureιdobutyronιtπle which is also known as "Kevetπn" This salt has the following formula

Kevetrin

In another embodiment the composition comprises the hydrobromide acid addition salt of 4- isothioureidobutyronitrile

In another embodiment the present invention relates to a pharmaceutical composition for the treatment of hyperprohferative diseases, including but not limited to cancer, inflammatory diseases, and viral and bacterial infections in mammals comprising an antihyperprohferative disease, antiinflammatory, antiviral or antibacterial effective amount of a compound selected from S-(2-cyanoethyl)ιsothιourea, S-(4- cyanobutyl)ιsothιourea , S-(5-cyanopentyl)ιsothιourea or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier

In another embodiment the present invention relates to a pharmaceutical composition for the treatment of hyperprohferative diseases, including but not limited to cancer, inflammatory diseases, and viral and bacterial infections in mammals comprising an antihyperprohferative disease, anti-inflammatory, antiviral or antibacterial effective amount of a compound selected from S-(4- cyanomethylphenyl)methylisothιourea hydrochloride, S-2(4-[2-cyanoethyl]phenyl)ethylisothiourea mesylate, S-(2-cyanomethylphenyl)methylisothiourea hydrochloride, S-(6-cyanomethylpyridin-2- yl)methylisothιourea hydrochloride, S-(3-cyanomethylphenyl)methylιsothiourea hydrochloride, S-(1-cyanomethylnaphth-2-yl))methylisothiourea hydrochloride or a different pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier. In another embodiment, the pharmaceutical composition comprises a compound selected from the compounds prepared as described in Example 11 set forth below or a different pharmaceutically acceptable salt thereof or a free base thereof and a pharmaceutically acceptable carrier.

In one embodiment of the invention the pharmaceutical composition does not include S- cyanomethylisothiourea HBr. In another embodiment of the invention the pharmaceutical composition does not include S-cyanomethylisothiourea HCI or S-cyanomethylisothiourea HBr. In another embodiment of the invention the pharmaceutical composition does not include pharmaceutically acceptable salts of S-cyanomethylisothiourea. In another embodiment of the invention the pharmaceutical composition does not include S-cyanomethylisothiourea as the free base or as a salt.

In one embodiment of the invention the pharmaceutical composition does not include S-(2- cyanoethyl)isothiourea HCI, S-cyanomethylisothiourea HBr and S-cyanomethylisothiourea HCI. In another embodiment of the invention the pharmaceutical composition does not include S-(2- cyanoethyl)isothiourea HCI, S-(2-cyanoethyl)isothiourea HBr, S-cyanomethylisothiourea HCI or S- cyanomethylisothiourea HBr. In another embodiment of the invention the pharmaceutical composition does not include pharmaceutically acceptable salts of S-(2-cyanoethyl)isothiourea and S- cyanomethylisothiourea. In another embodiment of the invention the pharmaceutical composition does not include S-(2-cyanoethyl)isothiourea as the free base or as a salt and does not include S- cyanomethyhsothiourea as the free base or as a salt.

In another embodiment of the present invention the pharmaceutical composition does not include S-(cyanomethyl)isothiourea HCI, S-(cyanomethyl)isothiourea HBr, S-(2-cyanoethyl)isothiourea HCI, S-(2-cyanoethyl)ιsothιourea HBr, S-(2-cyanoethyl)ιsothιourea p-toluenesulfonate, S-(3- cyanopropyl)isothiourea HCI, S-(3-cyanopropyl)isothiourea picrate, and S-para-cyanobenzylisothiourea HCI In another embodiment of the present invention the pharmaceutical composition also does not include the hydrobromide salt of S-(3-cyanopropyl)isothiourea or S-para-cyanobenzylisothiourea.

In another embodiment of the present invention the pharmaceutical composition does not include a pharmaceutically acceptable salt of S-(cyanomethyl)isothiourea, S-(2-cyanoethyl)isothiourea, S-(3- cyanopropyl)isothiourea, or S-para-cyanobenzylisothiourea. In another embodiment of the invention the compound is not selected from S-(cyanomethyl)isothiourea, S-(2-cyaπoethyl)isothiourea, S-(3- cyanopropyl)isothiourea and S-para-cyanobenzylisothiourea and pharmaceutically acceptable salts thereof. The pharmaceutically acceptable salts of the compounds of formula I include the acid addition and base salts (including disalts) thereof Suitable acid addition salts are formed from acids which form non-toxic salts Examples include the acetate, aspartate, benzoate, besylate, bicarbonate/carbonate, bisulphate/sulphate, borate, camsylate, citrate, edisylate, esylate, formate, fumarate gluceptate, gluconate, glucuronate, hexafluorophosphate, hibenzate, hydrochloride/chloride, hydrobromide/bromide, hydroiodide/iodide, isethionate, lactate, malate, maleate, malonate, mesylate, methylsulphate, naphthylate, 2-napsylate, nicotinate, nitrate orotate, oxalate, palmitate, pamoate, phosphate/hydrogen phosphate/dihydrogen phosphate, saccharate, stearate, succinate, tartrate, tosylate and tnfluoroacetate salts Suitable base salts are formed from bases which form non-toxic salts Examples include the aluminium, arginine, benzathine, calcium, choline, diethylamine, diolamine, glycine, lysine, magnesium meglumine, olamiπe, potassium, sodium, tromethamine and zinc salts For a review on suitable salts, see "Handbook of Pharmaceutical Salts Properties, Selection, and Use" by Stahl and Wermuth (Wiley-VCH, Weinheim, Germany, 2002)

A pharmaceutically acceptable salt of a compound of formula I may be readily prepared by mixing together solutions of the compound of formula I and the desired acid or base, as appropriate The salt may precipitate from solution and be collected by filtration or may be recovered by evaporation of the solvent The degree of ionisation in the salt may vary from completely ionised to almost non-ionised

The compounds of formula I and the pharmaceutically acceptable salts thereof (hereinafter also referred to as the active compounds) may exist in both unsolvated and solvated forms The active compounds (including, those in the form of salts, free bases, free acids and neutral compounds) may form hydrates and other solvates The term 'solvate' is used herein to describe a molecular complex comprising a compound of the invention and one or more pharmaceutically acceptable solvent molecules, for example, ethanol The term 'hydrate' is employed when said solvent is water Pharmaceutically acceptable solvates include hydrates and other solvates wherein the solvent of crystallization may be isotopically substituted, e g D ₂ O, d ₆ -acetone, d ₆ -DMSO The active compounds may exist as clathrates or other complexes In general, the solvated, hydrated and the like forms are equivalent to the unsolvated, unhydrated/anhydrous and the like forms and the compounds, compositions and uses claimed herein are intended to encompass these forms, as well as the isomeric, crystalline and amorphous forms and the isotopically labeled compounds discussed below, within the scope of the present invention

Compounds of formula I containing one or more asymmetric carbon atoms can exist as two or more stereoisomers Where a compound of formula I contains an alkenyl or alkenylene group or a cycloalkenyl group, geometric cis/trans (or Z/E) isomers are possible Where the compound contains, for example, a keto or oxime group or an aromatic moiety, tautomeric isomerism ('tautomerism') can occur It follows that a single compound may exhibit more than one type of isomerism The compounds of formula I may also exist as isomers if they form acid addition or base salts wherein the counterion is optically active, for example, D-lactate or L-lysine, or racemic, for example, DL-tartrate or DL-argιnine Mixtures of stereoisomers may be separated by conventional techniques known to those skilled in the art. See, for example, "Stereochemistry of Organic Compounds" by E L.. Eliel (Wiley, New York, 1994)

Cis/trans isomers may be separated by conventional techniques well known to those skilled in the art, for example, chromatography and fractional crystallisation

In general, enantiomerically pure compounds of the present invention can be prepared and can be isolated according to art-known processes such as, for example, chiral synthesis from a suitable optically pure precursor and resolution of a racemate (or a racemate of a salt or derivative). For example, a racemate (or a racemic precursor) may be separated using chiral high pressure liquid chromatography (HPLC). Alternatively, a racemate (or a racemic precursor) may be reacted with a suitable optically active compound, for example, an alcohol, or, in the case where the compound of formula I contains an acidic or basic moiety, with an acid or base such as tartaric acid or 1-phenylethylamine. The resulting diastereomeric mixture may be separated by chromatography or fractional crystallization or both and one or both of the diastereoisomers may be converted to the corresponding pure enantiomer(s) by means well known to a skilled person

Chiral compounds of the present invention (and chiral precursors thereof) may be obtained in enantiomerically-enriched form using chromatography, typically HPLC, on a resin with an asymmetric stationary phase and with a mobile phase consisting of a hydrocarbon, typically heptane or hexane, containing from 0 to 50% isopropanol, typically from 2 to 20%, and from 0 to 5% of an alkylamine, typically 0.1% diethylamine. Concentration of the eluate affords the enriched mixture.

In the solid state, the compounds of the present invention may exist in crystalline or amorphous form The present invention includes all pharmaceutically acceptable isotopically-labelled compounds of formula I claimed herein wherein one or more atoms are replaced by atoms having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number usually found in nature.

Examples of isotopes suitable for inclusion in the compounds of the invention include isotopes of hydrogen, such as ² H and ³ H, carbon, such as ¹¹ C, ¹³ C and ¹⁴ C, chlorine, such as ³⁶ CI, fluorine, such as ¹⁸ F, iodine, such as ¹²³ I and ¹²⁵ I ₁ nitrogen, such as ¹³ N and ¹⁵ N, oxygen, such as ¹⁵ 0, ¹⁷ O and ¹⁸ O, phosphorus, such as ³² P, and sulphur, such as ³⁵ S Certain isotopically-labelled compounds of formula I, for example, those incorporating a radioactive isotope, are useful in drug and/or substrate tissue distribution studies. The radioactive isotopes tritium, i.e. ³ H, and carbon-14, i.e. ¹⁴ C, are particularly useful for this purpose in view of their ease of incorporation and ready means of detection. Substitution with heavier isotopes such as deuterium, i.e. ² H, may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be preferred in some circumstances. Substitution with positron emitting isotopes, such as ¹¹ C, ¹⁸ F, ¹⁵ O and ¹³ N, can be useful in Positron Emission Topography (PET) studies for examining substrate receptor occupancy

Isotopically-labelled compounds of formula I can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying Examples using an appropriate isotopically-labeled reagent in place of the non-labeled reagent previously employed

The present invention also relates to a pharmaceutical composition for the treatment of cellular hyperproliferation comprising an antihyperproliferation effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier In another embodiment, the present invention relates to a pharmaceutical composition for the treatment of cancer comprising an anticancer effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier In another embodiment, the present invention relates to a pharmaceutical composition for the treatment of cancer comprising an apoptosis inducing effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier In other embodiments, one or more of the compounds excluded from the pharmaceutical compositions discussed above may be excluded from the pharmaceutical compositions referred to in this paragraph as well

The present invention also relates to a pharmaceutical composition in dosage unit form for the treatment of cellular hyperproliferation, including but not limited to cancer, comprising an antihyperproliferation or anticancer effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier In other embodiments, one or more of the compounds excluded from the pharmaceutical compositions discussed above may be excluded from the aforementioned pharmaceutical composition as well

The present invention also relates to a parenteral pharmaceutical composition for the treatment of cellular hyperproliferation, including but not limited to cancer, comprising an antihyperproliferation or anticancer effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier suitable for parenteral administration The pharmaceutical product can be obtained by dissolving a desired quantity of the product in a sterile isotonic solution which can be readily administered through any desired route In other embodiments, one or more of the compounds excluded from the pharmaceutical compositions discussed above may be excluded from the aforementioned pharmaceutical composition as well

The present invention also relates to a method of treating hyperprohferative diseases, including but not limited to cancer, inflammatory diseases, and viral and bacterial infections in mammals, including humans, comprising administering to a patient in need of such treatment an antihyperprohferative disease anti-inflammatory, antiviral or antibacterial effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof In one embodiment the compound is selected from S-(3- cyanopropyl)ιsothιourea, S-(2-cyanoethyl)ιsothιourea, S-(4-cyanobutyl)ιsothιourea , S-(5- cyanopentyl)ιsothιourea, S-(4-cyanomethylphenyl)methylιsothιourea, S-2(4-[2-cyanoethyl]phenyl)ethyhsothιourea, S-(2-cyanomethylpheπyl)methylιsothιourea, S-(6-cyanomethylpyπdιn-2-yl)methylιsothιourea, S-(3-cyanomethylphenyl)methylιsothιourea, and S-(1- cyanomethylnaphth-2-yl))methylisothiourea and the pharmaceutically acceptable salts thereof In another embodiment the compound is S-(3-cyanopropyl)isothιourea hydrochloride In another embodiment the compound is selected from the compounds prepared as described in Example 11 below, or a different pharmaceutically acceptable salt thereof or a free base thereof

The present invention also relates to a method of treating hyperproliferation comprising administering to a patient in need of such treatment an antihyperproliferation effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof In another embodiment, the present invention relates to a method of treating cancer comprising administering to a patient in need of such treatment an anticancer effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof In another embodiment, the present invention relates to a method of treating cancer comprising administering to a patient in need of such treatment an apoptosis inducing effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof In other embodiments, one or more of the compounds excluded from the pharmaceutical compositions discussed above may be excluded from the methods referred to in this paragraph as well

The present invention also relates to a method of treating head and neck cancer, non-small cell lung cancer, small cell lung cancer, resistant types of lung and any female cancers, ovarian cancer, breast cancer or colon cancer in a mammal in need of such treatment comprising administering to said mammal an anticancer effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof In one embodiment of the present invention the cancer is selected from head and neck cancer, non-small cell lung cancer, ovarian cancer and colon cancer In one embodiment of the present invention the head cancer is a glioma

The present invention also relates to a method of treating a hyperprohferative disease responsive to induction of apoptosis in a mammal in need of such treatment comprising administering separately, simultaneously, concurrently, sequentially or chronologically staggered to said mammal in need thereof, an amount of an active compound, which is a compound of formula I or a pharmaceutically acceptable salt thereof and an amount of at least one second compound or radiation, said second compound being an anti-cancer agent selected from the group consisting of chemotherapeutic anti-cancer agents and target-specific anti-cancer agents, wherein the amounts of the active compound and said second compound or radiation result in a therapeutic effect In one embodiment of the invention said second compound is selected from the group consisting of (ι) alkylating/carbamylating agents, (ιι) platinum derivatives, (in) antimitotic agents/tubuhn inhibitors, (ιv) topoisomerase inhibitors, (v) pyrimidine antagonists, (vι) purine antagonists, (vιι) folic acid antagonists, and (VIM) injected radioactive materials In one embodiment of the invention, said target-specific anti-cancer agent is selected from the group consisting of (ι) kinase inhibitors, (ιι) proteasome inhibitors, (in) histone deacetylase inhibitors (ιv) heat shock protein 90 inhibitors; (v) vascular targeting agents (VAT) anti-angiogenic drugs, and KDR tyrosine kinase inhibitors, (vi) monoclonal antibodies as well as mutants and conjugates of monoclonal antibodies and antibody fragments; (vii) oligonucleotide based therapeutics; (viii) Toll-like receptor/TLR 9 agonists, TLR 7 agonists and analogues thereof, or TLR 7/8 agonists as well as immunostimulatory RNA as TLR 7/8 agonists; (ix) protease inhibitors; (x) hormonal therapeutics; (xi) bleomycin; (xii) retinoids; (xiii) DNA methyltransferase inhibitors; (xiv) alanosine; (xv) cytokines; (xvi) interferons; and (xvii) death receptor agonists. In one embodiment of the invention, said compound of formula I or a pharmaceutically acceptable salt thereof is administered separately, simultaneously, concurrently, sequentially or chronologically staggered with an anti-cancer effective amount of radiation. It will be clear from the foregoing that as used herein the term "effective amount" includes an amount of an active compound that is effective when administered by itself as well as an amount of an active compound that is effective when administered in conjunction with another therapeutic agent.

The hyperproliferative diseases that may be treated by the methods of the present invention include, but are not limited to, cancer of the breast, bladder, bone, brain, central and peripheral nervous system, colon, endocrine glands, esophagus, endometrium, germ cells, head and neck, kidney, liver, lung, larynx and hypopharynx, mesothelioma, sarcoma, ovary, pancreas, prostate, rectum, small intestine, soft tissue, testis, stomach, skin, ureter, vagina and vulva; inherited cancers, retinoblastoma and Wilms tumor; leukemia, lymphoma, non-Hodgkms disease, chronic and acute myeloid leukemia, acute lymphoblastic leukemia, Hodgkins disease, multiple myeloma and T-cell lymphoma, myelodysplastic syndrome, plasma cell neoplasia, paraneoplastic syndromes, cancers of unknown primary site, drug resistant cancers and AIDS related malignancies and the disease is treated by administering to a mammal in need of such treatment an antihyperproliferation or anticancer effective amount of a compound of formula I or a pharmaceutically acceptable salt thereof In one embodiment of the invention, the hyperproliferative disease is selected from the group consisting of head and neck cancer, non-small cell lung cancer, small cell lung cancer, resistant types of lung and any female cancers, breast cancer, ovarian cancer and colon cancer.

The present invention also relates to a compound of the formula I as defined above or a pharmaceutically acceptable salt thereof with the proviso that the compound is not

S-(cyanomethyl)isothiourea HCI, S-(cyanomethyl)isothiourea HBr, S-(2-cyanoethyl)isothiourea HCI, S- (2-cyanoethyl)isothiourea HBr, S-(2-cyanoethyl)isothiourea p-toluenesulfonate, S-(3- cyanopropyl)isothiourea HCI, S-(3-cyanopropyl)isothiourea picrate, and S-para-cyanobenzylisothiourea HCI. In another embodiment of the present invention the compound is also not a hydrobromide salt of S- (3-cyanopropyl)isothiourea or S-para-cyanobenzylisothiourea

In another embodiment of the present invention the compound is not a pharmaceutically acceptable salt of S-(cyanomethyl)ιsothiourea, S-(2-cyanoethyl)isothiourea, S-(3-cyanopropyl)isothiourea, or S-para- cyanobeπzylisothiourea. In another embodiment of the invention the compound is not selected from S- (cyanomethyl)ιsothιourea, S-(2-cyanoethyl)ιsothιourea, S-(3-cyanopropyl)ιsothιourea and S-para- cyanobenzyhsothiourea and pharmaceutically acceptable salts thereof

It should be noted that S-cyanomethylisothiourea is also named Carbamimidothioic acid, cyanomethyl ester, S-(2-cyanoethyl)ιsothιourea is also named Carbamimidothioic acid, cyanoethyl ester, S-(3- cyanopropyl)ιsothιourea is also named Carbamimidothioic acid, cyanopropyl ester, and S-para- cyanobenzylisothiourea is also named Carbamimidothioic acid, (4-cyanophenyl)methyl ester

In one embodiment of the present invention the compound is selected from S-(4-cyanobutyl)isothιourea and S-(5-cyanopentyl)ιsothιourea and pharmaceutically acceptable salts thereof In another embodiment of the present invention the compound is selected from, S-(4- cyanomethylphenyl)methylιsothιourea hydrochloride, S-2(4-[2-cyanoethyl]phenyl)ethylιsothιourea mesylate, S-(2-cyanomethylphenyl)methylιsothιourea hydrochloride, S-(6-cyanomethylpyrιdιn-2- yl)methylιsothιourea hydrochloride, S-(3-cyanomethylphenyl)methylιsothιourea hydrochloride, S-(1-cyanomethylnaphth-2-yl))methylιsothιourea hydrochloride or different pharmaceutically acceptable salts thereof In another embodiment the compound is selected from the compounds prepared as described in Example 11 set forth below or different pharmaceutically salt thereof or a free base thereof

The present invention also relates to a process for preparing the hydrochloride acid addition salt of a compound of the formula I wherein Z is sulfur comprising reacting thiourea or a thiourea derivative of the formula

S = C - NR ¹ H NR ² R ³ wherein R ¹ , R ² and R ³ are as defined above for formula I with the appropriate nitrile derivative of the formula NC-(CH ₂ ) _n -W-(CH ₂ ) _m CI, wherein n, m and W are as defined above for the compound of the formula I, in water or water / alcohol solvent or in a polar solvent, at reflux temperature to afford the compound of formula I wherein Z is sulfur, and, if desired, preparing the free base or a different acid addition salt In one embodiment of the invention the solvent is selected from an alcohol selected from methanol, ethanol, isopropanol and mixtures of one or more of the foregoing alcohols with water

The present invention also relates to a process for preparing the hydrochloride acid addition salt of a compound of formula I wherein Z is selected from copper silver, gold, platinum, and halogen-containing moieties selected from CIO ₂ , BrO ₂ and 1O ₂ comprising reacting a compound of the formula NC-(CH ₂ ) _n -W- (CH ₂ ) _m CI, wherein n, m and W are as defined above for the compound of formula I with a salt of the respective metal or of the halogen - containing moiety to form an intermediate compound and then reacting the intermediate compound with thiourea or a thiourea derivative of the formula

S = C - NR ¹ H NR ² R ³ wherein R ¹ , R ² and R ³ are as defined above for formula I to afford the a compound of formula I wherein Z is copper, silver, gold, platinum or a halogen-containing moiety selected from CIO ₂ , BrO ₂ , and 1O ₂ wherein the formation of the intermediate and the formation of the acid addition salt are conducted in water or water / alcohol solvent or in a polar solvent, at reflux temperature, and, if desired, preparing the free base or a different acid addition salt. In one embodiment of the invention the solvent is selected from an alcohol selected from methanol, ethanol, isopropanol and mixtures of one or more of the foregoing alcohols with water. The present invention also relates to the preparation of hydrobromide acid addition salts of the compound of formula I and the mesylate salts of the compound of formula I. The hydrobromide acid addition salts are prepared by substituting a bromine containing starting material in the processes described above The mesylate salts are prepared by substituting a mesylate starting material in the processes described above. A disalt of the present invention may be similarly prepared by using a salt as the starting material. It may be possible to form such a salt if the free base has two basic centers

Brief Description of the Drawings

Figure 1 shows the time dependence of Kevetrin cytotoxicity Human carcinoma cells were exposed to different concentrations of Kevetrin for 5, 10, 20, 30, or 45 minutes or 1 , 2, 6, 24, or 120 hours. Cellular viability expressed as IC50 was plotted verses time of Kevetrin exposure as measured using the MTT assay.

Figure 2 shows activity spectra for Kevetrin and Cisplatiπ The influence of Kevetrin and cisplatin on the viability of the indicated tumor cell lines was measured using the MTT assay after continuous exposure to Kevetrin for three doubling times. The indicated values are calculated as follows: log (IC ₅₀ individual cell line - IC ₅₀ average). Negative values indicate that the cell line is more sensitive than the average, whereas positive values indicate that the cell line is more resistant than the average. The average IC ₅₀ S for all cell lines tested were 4.9 x 10 ^"7 M for Kevetrin, and 2.1 x 10 ^"6 M for cisplatin.

Figure 3 shows the weight changes of mice due to Kevetrin. Animal weights of mice following treatment with either 100 or 200 mg/kg Kevetrin IV on Day 0 are shown

Figure 4 shows the efficacy of Kevetrin or Taxol in mammary carcinoma. MDA-MB-231 human breast carcinoma bearing mice were treated with 200 mg/kg Kevetrin IV days 7, 9, and 11 compared to 22 mg/kg Taxol IV Days 7,9,11 and 13.

Figure 5 shows the efficacy of Kevetrin or 5-FU in colon carcinoma. HT-29 tumor bearing nude mice were treated with either 200 mg/kg Kevetrin IV or 5-FU on Days 7, 9, and 11

Figure 6 shows the efficacy of Kevetrin or cisplatin in prostate cancer PC-3 tumor bearing nude mice were treated with either 200 mg/kg Kevetrin IV on Days 7, 9, 11 or 10 mg/kg cisplatin on Day 7.

Figure 7 shows the efficacy of Kevetrin or Taxol in human P-glycoprotein mediated resistant colon carcinoma. HCT-15 tumor bearing nude mice were treated with either 200 mg/kg Kevetrin IV on Days 7, 9, 11 or 22 mg/kg Taxol on Days 7, 9, 11 and 13 post tumor. Figure 8 shows efficacy of Kevetπn 200 mg/kg on days 7,9 and 11 and against Taxol at 22 mg/kg on days 7,9,11 and 13 in A549 multi-drug resistant human lung carcinoma

Figure 9 shows efficacy of Kevetrin 200 mg/kg on days 7,9 and 11 and against Taxol at 22 mg/kg on days 7,9,11 and 13 in NCI-H 1975 multi-drug resistant human lung carcinoma Detailed Description of the Invention

Compounds useful in the present invention wherein Z is sulphur are prepared by reacting thiourea with the appropriate nitrile derivative of the formula NC-(CH ₂ ) _n -W-(CH ₂ ) _m CI, wherein n, m, and W are as defined above for the compound of the formula I ₁ in water Equal amounts of thiourea and a nitrile are added to a 10x volume of water or water/ alcohol solvent, or polar solvent, and heated to reflux for about 4 hours at ambient pressure Non-limiting examples of suitable alcohols for preparing mixtures of water and alcohol or for use as polar solvents include methanol ethanol and and isopropanol The reaction mixture is allowed to evaporate yielding the desired product This product is purified by recrystallization from ethanol or another suitable solvent, for example, isopropanol or methanol or mixtures of one of the foregoing alcohols with acetone The crystalline material is collected by filtration and dried under a high vacuum Compounds of formula I wherein Z is selected from copper, silver, gold and platinum, or Z is a halogen-containing moiety selected from CIO ₂ , BrO ₂ , and 1O ₂ are similarly prepared

Compounds of formula I wherein Y in the W moiety is sulphur, oxygen or nitrogen are prepared by selecting the appropriate nitrile derivative wherein sulphur, oxygen or nitrogen is in the desired position on a ring in the W moiety

One of ordinary skill in the art would know how to select conditions from those discussed above or to make modifications thereto in order to make specific compounds of interest

Depending on the disease and condition of the patient, the term "treatment" as used herein may include one or more of curative palliative and prophylactic treatment The active compounds may be administered, in the treatment of a patient, together with radiation or with other antihyperproliferation compounds such as one or more of cyclophosphamide cisplatin, carboplatin Taxol, and Erbitux, as well as other approved antihyperproliferation compounds, in combination or sequentially Depending on the particular disorder and the condition of the patient, such treatment may be more effective than either compound alone or radiation alone The precise dosage administered of each active compound for antihyperproliferation, anti inflammatory, antibacterial or antiviral use will vary depending upon a number of factors including but not limited to the type of patient and type of disease state being treated, the age of the patient, and the route(s) of administration

For administration to human patients, the total daily dose of the active compounds is anticipated to be in the range of 1 mg to 300 mg per kg of body weight, depending on the mode of administration For example, oral administration may require a total daily dose of from 100 mg to 300 mg per kg of body weight, while an intravenous dose may only require from 20 mg to 200 mg per kg of body weight The total daily dose may be administered in single or divided doses For an average human subject having a weight of about 70 kg, the dosage would be about 1400 mg to 21000 mg for oral administration and about 140 mg to 1400 mg for intravenous administration The physician will readily be able to determine doses for subjects whose weight falls outside this range, such as infants and the elderly A veterinarian will readily be able to determine doses for other mammals

In one embodiment, the invention comprises administration of an intravenous solution or suspension comprising 200 mg of an active compound per kg of body weight For the above-mentioned therapeutic uses, the dosage administered will, of course, vary with the compound employed, the mode of administration, the treatment desired and the disorder indicated The total daily dose may be administered in single or divided doses The present invention also encompasses sustained release compositions

The pharmaceutical composition may, for example, be in a form suitable for oral administration as a tablet, capsule, pill, powder, sustained release formulation, solution, suspension, for parenteral injection as a sterile solution, suspension or emulsion, for topical administration as an ointment or cream or for rectal administration as a suppository The pharmaceutical composition may be in unit dosage forms suitable for single administration of precise dosages The pharmaceutical composition will include a conventional pharmaceutical carrier or excipient and an active compound In addition, it may include other medicinal or pharmaceutical agents, carriers, adjuvants, etc

Exemplary parenteral administration forms include solutions or suspensions of active compounds in sterile aqueous solutions, for example, aqueous propylene glycol or dextrose solutions Such dosage forms can be suitably buffered, if desired

Suitable pharmaceutical carriers include inert diluents or fillers, water and various organic solvents The pharmaceutical compositions may if desired, contain additional ingredients such as flavorings, binders, excipients and the like Thus for oral administration, tablets containing various excipients, such as citric acid may be employed together with various disintegrants such as starch, alginic acid and certain complex silicates and with binding agents such as sucrose, gelatin and acacia Additionally, lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often useful for tableting purposes Solid compositions of a similar type may also be employed in soft and hard filled gelatin capsules Useful components of these compositions include lactose or milk sugar and high molecular weight polyethylene glycols When aqueous suspensions or elixirs are desired for oral administration the active compound therein may be combined with various sweetening or flavoring agents, coloring matters or dyes and, if desired, emulsifying agents or suspending agents, together with diluents such as water, ethanol, propylene glycol glycerin, or combinations thereof

Methods of preparing various pharmaceutical compositions with a specific amount of active compound are known, or will be apparent, to those skilled in this art For examples, see Remington's Pharmaceutical Sciences. Mack Publishing Company, Easter, Pa , 15th Edition (1975) The dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition For example, doses may be adjusted based on pharmacokinetic or pharmacodynamic parameters, which may include clinical effects such as toxic effects and/or laboratory values Thus, the present invention encompasses intra-patient dose-escalation as determined by the skilled artisan Determining appropriate dosages and regimens for administration of the chemotherapeutic agents are well-known in the relevant art and would be understood to be encompassed by the skilled artisan once provided the teachings disclosed herein

A pharmaceutical composition of the invention may be prepared, packaged, or sold in bulk, as a single unit dose, or as a plurality of single unit doses As used herein, a "unit dose" is a discrete amount of the pharmaceutical composition comprising a predetermined amount of the active compound The amount of the active compound is generally equal to the dosage of the active compound which would be administered to a subject or a convenient fraction of such a dosage such as, for example, one-half or one-third of such a dosage

The relative amounts of the active compound the pharmaceutically acceptable carrier, and any additional ingredients in a pharmaceutical composition of the invention will vary, depending upon the identity, size, and condition of the subject treated and further depending upon the route by which the composition is to be administered By way of example, the composition may comprise between 0 1% and 100% (w/w) active ingredient

In addition to the active compound, a pharmaceutical composition of the invention may further comprise one or more additional therapeutically effective compounds as discussed above

As used herein, "parenteral administration" of a pharmaceutical composition includes any route of administration characterized by physical breaching of a tissue of a subject and administration of the pharmaceutical composition through the breach in the tissue Parenteral administration thus includes, but is not limited to, administration of a pharmaceutical composition by injection of the composition by application of the composition through a surgical incision, by application of the composition through a tissue-penetrating non-surgical wound, and the like Thus, the active compounds may be administered directly into the blood stream, into muscle, or into an internal organ Suitable means for parenteral administration include intravenous, intraarterial, intraperitoneal, intrathecal, intraventricular, intraurethral, intrasternal, intracranial, intramuscular and subcutaneous, and kidney dialytic infusion techniques Suitable devices for such parenteral administration include needle (including microneedle) injectors, needle-free injectors and infusion apparatus

Parenteral formulations are typically aqueous solutions which may contain excipients such as salts, carbohydrates and buffering agents (preferably to a pH of from 3 to 9), but, for some applications, they may be more suitably formulated as a sterile non-aqueous solution or as a dried form to be used in conjunction with a suitable vehicle such as sterile, pyrogen-free water The preparation of parenteral formulations under sterile conditions, for example by lyophilisation, may readily be accomplished using standard pharmaceutical techniques well known to those skilled in the art

Formulations of a pharmaceutical composition suitable for parenteral administration comprise the active ingredient combined with a pharmaceutically acceptable carrier, such as sterile water or sterile isotonic saline Such formulations may be prepared, packaged, or sold in a form suitable for bolus administration or for continuous administration Injectable formulations may be prepared, packaged, or sold in unit dosage form, such as in ampules or in multi-dose containers containing a preservative Formulations for parenteral administration include, but are not limited to, suspensions, solutions, emulsions in oily or aqueous vehicles, pastes, and implantable sustained-release or biodegradable formulations as discussed below Such formulations may further comprise one or more additional ingredients including, but not limited to, suspending, stabilizing, or dispersing agents In one embodiment of a formulation for parenteral administration, the active ingredient is provided in dry (ι e powder or granular) form for reconstitution with a suitable vehicle (e g sterile pyrogen-free water) prior to parenteral administration of the reconstituted composition

The pharmaceutical compositions may be prepared, packaged, or sold in the form of a sterile injectable aqueous or oily suspension or solution This suspension or solution may be formulated according to the known art, and may comprise, in addition to the active ingredient, additional ingredients such as the dispersing agents, wetting agents, or suspending agents described herein Such sterile injectable formulations may be prepared using a non-toxic parenterally-acceptable diluent or solvent, such as water or 1 ,3-butane diol, for example Other acceptable diluents and solvents include, but are not limited to, Ringer's solution, isotonic sodium chloride solution, and fixed oils such as synthetic mono- or dι- glycendes Other parentally-administrable formulations which are useful include those which comprise the active ingredient in microcrystalline form, in a liposomal preparation, or as a component of a biodegradable polymer system Compositions for sustained release or implantation may comprise pharmaceutically acceptable polymeric or hydrophobic materials such as an emulsion, an ion exchange resin, a sparingly soluble polymer, or a sparingly soluble salt

The active compounds are inhibitors of cellular hyperproliferation or are cell-cycle specific inducers of apoptosis in cancer cells or are both Therefore, these compounds are useful for treating hyperproliferative diseases and disorders such as cancer, and are useful for treating diseases and disorders that are responsive to the induction of apoptosis, such as cancer By having a cell-cycle specific mode of action, these compounds should have a higher therapeutic index compared to standard chemotherapeutic drugs targeting basic cellular processes like DNA replication or interfering with basic cellular molecules like DNA Thus, for example, the active compounds discussed herein are expected to be useful in targeted cancer therapy The active compounds may also be effective against angiogenesis

In the context of this invention, hyperproliferation and analogous terms are used to describe aberrant or deregulated, or aberrant and deregulated, cellular growth, a hallmark of diseases like cancer Inhibition of cell proliferation and analogous terms are used herein to denote an ability of the compound to retard the growth of and/or kill a cell contacted with that compound as compared to cells not contacted with that compound Most preferably this inhibition of cell proliferation is 100%, meaning that proliferation of all cells is stopped and/or cells undergo programmed cell death In some embodiments the contacted cell is a neoplastic cell A neoplastic cell is defined as a cell with aberrant cell proliferation A benign neoplasia is described by hyperproliferation of cells, incapable of forming an aggressive, metastasizing tumor ιn- vivo In contrast, a malignant neoplasia is described by cells with different cellular and biochemical abnormalities, e g capable of forming tumor metastasis The acquired functional abnormalities of malignant neoplastic cells (also defined as ' hallmarks of cancer") are replicative potential ("hyperproliferation"), self-sufficiency in growth signals, insensitivity to anti-growth signals evasion from apoptosis, sustained angiogenesis and tissue invasion and metastasis

Inducer of apoptosis and analogous terms are used herein to identify a compound which executes programmed cell death in cells contacted with that compound Apoptosis is defined by complex biochemical events within the contacted cell, such as the activation of cystein specific proteinases ("caspases") and the fragmentation of chromatin Induction of apoptosis in cells contacted with the compound might not necessarily be coupled with inhibition of cell proliferation Preferably, the inhibition of cell proliferation and/or induction of apoptosis is specific to cells with aberrant cell growth (hyperproliferation) Thus, compared to cells with aberrant cell growth, normal proliferating or arrested cells are less sensitive or even insensitive to the proliferation inhibiting or apoptosis inducing activity of the compound Finally, cytotoxic is used in a more general sense to identify compounds which kill cells by various mechanisms, including the induction of apoptosis/programmed cell death in a cell cycle dependent or cell-cycle independent manner

Cell cycle specific and analogous terms are used herein to identify a compound as inducing apoptosis only in continuously proliferating cells actively passing a specific phase of the cell cycle, but not in resting, non-dividing cells Continuously proliferating cells are typical for diseases like cancer and characterized by cells in all phases of the cell division cycle namely in the G ("gap") 1 , S ("DNA synthesis"), G2 and M ("mitosis") phase

AKT (also known as protein kinase B (PKB)), and its gene family products, has been identified as a serine/threonine protein kinase Testa et al , Proc Natl Acad Sci , 2001 , 98, 10983-10985, Lawlor et al , J Cell Sci 2001 , 114, 2903-2910, Duan, Circ Res , 2000, 86, 15-23 PKB plays an important role in cell proliferation, apoptosis and response to insulin Accordingly, modulation of PKBs is of interest in the treatment of tumorigenesis, abnormal cell proliferation, and diabetes In the context of this invention, hyperproliferation and analogous terms are used to describe aberraπt/disregulated cellular growth, a hallmark of diseases like cancer

PKB Assay A kinase assay for evaluating PKB activity comprises active PKB enzymes a PPKB specific substrate and P ³³ -labeled ATP Two forms of PKBa enzymes are used, the full length PKBα and a kinase domain of PKBα with pleckstrin domain (amino acids 1-117) deleted Both PKB enzymes are available from Upstate Cell Signaling Solutions (Catalog Numbers 14-276 and 14-341) The PKB substrate used is a synthetic peptide (ARKRERTYSFGHHA) as described in Obata et al , J Biol Chem 2000, 275, 36108- 36115 The phosphorylated substrate is captured by a phosphocellulose membrane filter plate (Milhpore) and measured by a Wallac Microbeta liquid scintillation counter (Perkin Elmer)

PKB activity in cells is assayed in a PTEN null human breast tumor cell line MDA-MB 468 The phosphorylation status of PKB substrate FKHRL1 , GSK3a/b, and Tuberin are measured by immunoassays utilizing phospho-specific antibodies (Cell signaling technology)

The effect of PKB inhibition on cell viability is measured in a range of human tumor cell lines including but not limiting to MDA-MB-468, MDA-MB-231 , U87-MG, LN-229, PC-3, DU145 The cells are treated in regular growth media for 72 hours and cell viability is measured by Alamar Blue (Biosource, UK) The following non-limiting Examples illustrate the preparation of the active compounds

¹ H Nuclear magnetic resonance (NMR, Mercury- 300) spectra were consistent with the proposed structures Characteristic chemical shifts (δ) are given in parts-per-milhon downfield from tetramethylsilane using conventional abbreviations for designation of major peaks e g s, singlet, d, doublet t triplet, q, quartet, m, multiplet, br, broad The mass spectra (m/z) were recorded on an Agilent model 1100 mass spectrometer using either electrospray ionisation (ESI) or atmospheric pressure chemical ionisation (APCI) The following abbreviations have been used for common solvents CDCI ₃ deuterochloroform, D ₆ -DMSO deuterodimethylsulphoxide, CD ₃ OD deuteromethanol

Example 1 S-(3-cyanopropyl)ιsothιourea hydrochloride (also known as Kevetrin) HCl

The γ-Chlorobutyronitnle (5 0 g, 48 3 mmol) and thiourea (4 04 g, 53 1 mmol) were mixed in 40 ml of water The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated and 20 ml of ethanol was added and then evaporated as well This was repeated three times After that, 10 ml of methanol and 30 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 544 g (30 3 mmol, yield 62 7%) of product as white crystals, melting point 134-135°C, with purity greater than 97% ¹ H NMR (300 MHz, d ₆ DMSO) § 1 89 (m, 2 H), 2 63 (t, 2H, J = 7 2 Hz), 3 23 (t, 2H, J = 7 2 Hz) 3 38 (s, 3H) ¹³ C NMR (75 MHz) δ 15 3, 25 0, 28 8 119 8, 169 7

Formula C ₅ H ₁₀ CIN ₃ S

Exact Mass 179 03

MoI Wt 179 67 m/e 17903 (1000%), 18103 (321%), 18003 (74%), 18102 (45%), 18203 (20%), 18302 (15%) C 3342, H, 561,Cl, 1973, N, 2339, S, 1785 Anal Calcd 334256123391785 Found. 33.44 5.48 23.40 18.31

Example 2

S-(2-cyanoethyl)isothiourea hydrochloride

N^ _/ C, + X . N^^S _T NH HC,

NH^ ^NH ₂ NH ₂

^C3h4CIN CH ₄ N ₂ S C ₄ H ₆ CIN ₃ S

^M ° ^{I Wt 89 52} Mo. W. 76.12 MOl W. 165 64

The 3-chloropropanenιtrιle (4.32 g, 48.3 mmol) and thiourea (4.04 g, 53.1 mmol) are mixed in 40 ml of water. The mixture is heated to reflux for 3 to 4 hours. The reaction mixture is evaporated and 20 ml of ethanol is added and then evaporated as well. This is repeated three times. After that, 10 ml of methanol and 30 ml of acetone are added and the mixture is stirred for one hour. The crystalline material is filtered and the product is dried under high vacuum overnight to obtain S-(2-cyanoethyl)isothiourea hydrochloride Example 3

S-(4-cyanobutyl)isothiourea hydrochloride s

A ^NH HCI

NH/- "NH, ,-. ^ " " Υ

^C 5 ^H 8CIN CH^N ₂ S ^NH2

C ₆ H ₁₂ CIN ₃ S M ^O l Wt 117 58 _M0 | WI . 76 12

MoI Wt 1937

The 5-chloropentanenitrile (5.68 g, 48.3 mmol) and thiourea (4.04 g, 53.1 mmol) are mixed in 40 ml of water. The mixture is heated to reflux for 3 to 4 hours. The reaction mixture is evaporated and 20 ml of ethanol are added and then evaporated as well This is repeated three times. After that, 10 ml of methanol and 30 ml of acetone are added and the mixture is stirred for one hour. The crystalline material is filtered and the product is dried under high vacuum overnight to yield S-(4-cyanobutyl)isothiourea hydrochloride

Example 4

S-(5-cvanopentyl)isothiourea hydrochloride

MoI Wt 76.12 MoI Wt 20772

The 6-chlorohexanenitrile (6.36 g, 48.3 mmol) and thiourea (4.04 g, 53.1 mmol) are mixed in 40 ml of water. The mixture is heated to reflux for 3 to 4 hours The reaction mixture is evaporated and 20 ml of ethanol is added and then evaporated as well. This is repeated three times After that, 10 ml of methanol and 30 ml of acetone are added and the mixture is stirred for one hour The crystalline material is filtered and the product is dried under high vacuum overnight to yield S-(5-cyanopentyl)isothιourea hydrochloride. Example 5 S-(4-cvanomethylphenyl)methylisothιourea hydrochloride

C ₉ H ₈ CIN CH ₄ N ₂ S C ₁₀ Hi ₂ ON ₃ S MoI Wl 165 62 MoI Wt 76 12 Md Wl 241 74

The 4-chloromethylphenylacetonιtπle (200 mg, 1 21 mmol) and thiourea (101 mg 1 33 mmol) were mixed in 1 ml of methanol The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 219 mg (0 91 mmol, yield 75 %) of product as off white crystals, with purity greater than 95% ¹ H NMR (300 MHz, d ₆ -DMSO) ξ 4 03 (s, 2 H), 4 50 (s, 2H), 7 35 (d, 2H, J = 8 23 Hz), 745 (d, 2H, J = 8 23 Hz) 9 22 (s, 4H) (M + H) 206 00

Formula C ₁₀ H ₁₂ CIN ₃ S Exact Mass 241 04 (205 07) MoI Wt 241 74 m/e 241 04 (100 0%), 243 04 (36 6%), 242 05 (11 0%), 244 04 (4 6%), 242 04 (1 9%), 245 04 (1 5%)

Example 6

S-2(4-r2-cvanoethyllphenyltethylιsothιourea mesylate

C ₁₂ H ₁₅ NO ₃ S MoIWt 7612 C ₁₃ H ₁₉ N ₃ O ₃ S ₂ MoI Wt 253 32 MoI Wt 329 44

The mesylate (200 mg, 0 79 mmol) and thiourea (66 mg, 0 87 mmol) were mixed in 1 ml of methanol The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 203 mg (0 62 mmol, yield 78%) of product as off white crystals, with purity greater than 95% ¹ H NMR (300 MHz, d ₆ -DMSO) δ 2 35 (S, 3H), 2 80 (m, 2H), 2 85 (m, 2H), 2 91 (t, 2H, J = 7 4), 342 (t, 3H, J = 7 4), 7 24 (s, 4H) 9 04 (s, 4H) (M + H) 234 07 Formula C ₁₃ H ₁₉ N ₃ O ₃ S ₂

Exact Mass 329 09 (233 10) MoI Wt 32944 m/e 329 09 (100 0%) 330 09 (16 0%), 331 08 (9 1 %), 331 09 (1 9%), 332 09 (1 4%) 330 08 (1 1%) Example 7 S-(2-cvanomethv[phenyl)methylisothiourea hydrochloride

MoI Wt 241 74

The 2-chlormethylphenylacetonιtrιle (200 mg, 1 21 mmol) and thiourea (101 mg, 1 33 mmol) were mixed in 1 ml of methanol The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 231 mg (0 95 mmol, yield 79%) of product as off white crystals, with purity greater than 95% H NMR (300 MHz, d ₆ -DMSO) 5 4 14 (s, 2H) 4 56 (s, 2H), 7 37 (m, 2H), 745 (m, 2H), 9 23 (s, 4H) (M + H) 205 97 Formula C ₁₀ H ₁₂ CIN ₃ S

Exact Mass 241 04 (205 07) MoI Wt 241 74 m/e 241 04 (100 0%), 243 04 (36 6%), 242 05 (11 0%), 244 04 (4 6%), 242 04 (1 9%), 245 04 (1 5%)

Example 8

S-(6-cvanomethylpyridin-2-vhmethylisothiourea hydrochloride

The β-chloromethyl^-pyπdylacetonitπle (200 mg, 1 20 mmol) and thiourea (101 mg, 1 32 mmol) were mixed in 1 ml of methanol The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 216 mg (0 89 mmol, yield 74%) of product as off white crystals, with purity greater than 95% H NMR (300 MHz d _β -DMSO) 5 4 29 (s, 2H), 4 64 (s, 2H), 7 41 (d 1 H, J = 7 78), 7 51 (d, 1 H, J = 7 78), 7 91 (t, 1 H, J = 7 78) 9 46 (s, 4H) (M + H) 207 00 Formula C ₉ H ₁₁ CIN ₄ S

Exact Mass 242 04 (206 06) MoI Wt 242 73 m/e 242 04 (100 0%), 244 04 (36 7%), 243 04 (12 0%), 245 04 (3 9%), 246 03 (1 5%) Example 9 S-O-cvanomethylphenvDmethylisothiourea hydrochloride

The 3-bromomethylphenylacetonιtπle (200 mg, 0 95 mmol) and thiourea (80 mg, 1 05 mmol) were mixed in 1 ml of methanol The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 215 mg (0 75 mmol, yield 79%) of product as off white crystals, with purity greater than 95% H NMR (300 MHz, d _e -DMSO) § 4 08 (s, 2H), 4 53 (s, 2H), 7 31 (m, 2H), 740 (m, 2H), 9 25 (s, 4H) (M + H) 206 00

Formula Ci ₀ Hi ₂ BrN ₃ S

Exact Mass 284 99 (205 07)

MoI Wt 286 19 m/e 28699 (1000%), 28499 (981%), 28799 (127%), 28600 (107%), 28899 (45%) 28599

(19%)

Example 10

S-(1-cvanomethylnaphth-2-yl))methylιsothιourea hydrochloride

12 C ₁₄ H ₁₄ BrN ₃ S Molecular Weight 336 25

The 2-bromomethyl-1-napthylacetonιtrιle (200 mg, 0 77 mmol) and thiourea (64 mg, 0 85 mmol) were mixed in 1 ml of methanol The mixture was heated to reflux for 3 to 4 hours The reaction mixture was evaporated After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour The crystalline material was filtered and the product was dried under high vacuum overnight to yield 215 mg (0 64 mmol, yield 83%) of product as off white crystals, with purity greater than 95% H NMR (300 MHz, d _β -DMSO) δ 4 57 (s, 2H), 4 83 (s, 2H), 7 63 (m, 2H), 7 72 (m, 1 H), 8 05 (m, 2H), 8 2 (d, 1 H, J = 8 24), 9 1 (s, 2H), 9 28 (s 2H) (M + H) 256 00

Formula C ₁₄ H ₁₄ BrN ₃ S Exact Mass 335 01 (255 08) MoI Wt 336 25 m/e 335 01 (100 0%), 337 01 (97 6%), 336 01 (17 1 %), 338 01 (164%), 337 00 (4 5%), 339 00 (4 4%), 339 01 (1 4%), 338 00 (1 1%), 33702 (1 1%)

Example 11 Depicted below are chemical reactions showing the preparation of compounds of the invention. As illustrated, these compounds may be prepared in a manner analogous to that of Example 1 by reacting an appropriate nitrile derivative with thiourea Thiourea may be replaced by derivatives where one, two or three of the four substituents on the nitrogen atoms are other than hydrogen to provide other compounds of the formula I.

In the reactions depicted in this Example n and m are zero or independently integers from 1 to 8 and R ¹ , R ² , R ³ , and R ⁴ may be, for example, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, -CH ₂ -cyclopropyl, vinyl, allyl, n-butyl, sec-butyl, isobutyl, tert-butyl, cyclobutyl, -CH ₂ -cyclobutyl, n-pentyl, sec-pentyl, isopentyl, tert-pentyl, cyclopentyl, -CH ₂ -cyclopentyl, n-hexyl, sec-hexyl, cyclohexyl, -CH ₂ -cyclohexyl moieties and the like, which again, may bear one or more substituents. R ¹ , R ² , R ³ , and R ⁴ may also be alkenyl and alkynyl.. Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, and the like Representative alkynyl groups include, but are not limited to, ethynyl, 2-propynyl (propargyl), and 1-propynyl

The hydrochloride salts prepared as described above may be converted to the corresponding free base or to other pharmaceutically acceptable salts by known methods. Other pharmaceutically acceptable salts may also be prepared by substituting an appropriate starting material (for example, a bromine containing nitrile rather than a chlorine containing nitrile) for the nitrite in each of the above reactions.

Example 12 - Kevetrin Efficacy Studies Chemicals. Cells and Media

Kevetrin was synthesized as described in Example 1 Cisplatin, Vincristine, 5-FU and Taxol were purchased from Sigma Scientific. H460 and H522 lung carcinoma cells; HT-29, SW-620, and Colo 205, and HCT-15 colon carcinoma cells, OvCar-3, and SKOv-3 ovarian carcinoma cells; DU-145 and PC-3 prostate carcinoma cells, as well as SNB-19 and U-251 glioma cells, HT-1080 fibrosarcoma and SW-480 colon carcinoma cells were purchased from American Type Culture Collection (ATCC) (Rockville, MD) A2780 ovarian carcinoma cells and their cisplatin-resistant variants A2780/CP1 and A2780/CP2 were generated and characterized in-house Colon HCT-116 colon carcinoma cells and their p53 -/- and p21 - /- sub-lines were generously provided by Dr Gangadharan of Central Research Institute, Salem, Ohio whereas HCT-116 supplemented with chromosome 3 was obtained from The Rajiv Gandhi Center for Cancer Research (Rohmi, Delhi, India) Except as otherwise indicated, medium and other reagents were purchased from Becton Dickinson Basal culture medium (RPM 1-1640) manufactured by Bio Whittaker was sterilized through a 0 22 μm Millex-GV filter unit (Millipore) The prepared medium was stored in small ahquots at 5°C in the dark The basal culture medium was supplemented with 10% fetal calf serum (FCS-heat inactivated at 560 C for 30 minutes) for its use as culture medium and mitogen, i e , Lipopolysaccharide (LPS, 10-50 μg/ mL), was added to proliferate the cells

Growth Inhibition Assays

The cytotoxicity was determined by the Maximum Tolerated Titer (MTT) assay Briefly, cells were seeded in 24-well tissue culture plates at 10,000-15,000 cells/well and incubated overnight The exponentially growing cells were then exposed to different drug concentrations for three to four generation times Cellular viability was determined by exposing cells to the MTT tetrazolium salt for 4 hours at 37 ⁰ C, and the formation of Formazan was measured at 560 nm by a microplate reader The concentration inhibiting cell growth by 50% compared with untreated controls was determined from the curves plotting survival as a function of dose All values are the average of at least three independent experiments each done in duplicates

Cell Proliferation Assay MTT solution (10 μL) was added to all wells of 48 hour cultured lymphocytes and incubated for 4 hours at 37°C Two sets of cultures were prepared, LPS was added to one set only During this period, Formazan crystals formed at the bottom of each well Spent media along with suspension of cultured cells was removed by pipetting Then acidified isopropanol (100 μL of 0 1 N HCI in anhydrous isopropanol ) was added to all wells and mixed thoroughly to dissolve the dark blue crystals After a few minutes at room temperature, plates were read using a plate analyzer with a dual wavelength measuring system test wavelength of 540 nm, reference wavelength of 630 nm Plates were read within 1 hour of adding the acidified isopropanol Cell proliferation was calculated as a stimulation index

A540 nm with LPS

Stimulation index = A540 nm without LPS

Where A 540 = Absorbance at 540 nm Immunolocalization of p53

To determine the localization of p53, a protein that causes proliferation of cells, immunocytochemistry was carried out Briefly, HCT 116 cells (ATCC) were attached to glass slides overnight and exposed to isotoxic concentrations of Kevetrin (300 ng/ml), or cisplatin (11 μg/ml) for 6 hours After drug exposure cells were fixed with 3 7% formaldehyde, permeabilized with 0 25% Triton X-100, and blocked with 1% BSA (Bovine Serum Albumin) Cells were then incubated for 1 hour with antι-p53 polyclonal antibodies (Sc-6243, Santa Cruz Biotechnology California) followed by secondary anti-rabbit FITC-conjugated antibodies (Amersham Life Sciences, U K ) Covershps were mounted in Vectashield (Vector Laboratories Vector, LJ K ) and analyzed with an epifluorescence microscope Axiovert 100M equipped with appropriate filters and laser confocal scanning system LSM 510 by using a plan Apochromat x63 objective (Zeiss)

Western Blot Analysis

Western blot analysis was performed Whole cell lysates were prepared from cells treated with isotoxic concentrations of Kevitren (300 ng/ml), or cisplatin (11 μg/ml) for 6 hours Proteins (50 μg/lane) were separated on a 4-12% polyacrylamide SDS gel and transferred to PolyScreen membranes (Milhpore Bedford, MA) The presence of p53 p21 , and β-actm was revealed by antι-p53 antibodies (Sc-6243, Santa Cruz Biotechnology), antι-p21 antibodies (Sc-3976, Santa Cruz Biotechnology), and anti-actin antibodies (Sc-1616, Santa Cruz Biotechnology), respectively, followed by incubation with peroxidase- conjugated secondary antibodies (Jackson ImmunoResearch, West Grove, PA) and detection by enhanced chemiluminescence (New England Nuclear, Hebron, CT)

Influence of Kevetrin on the Viability of Human Tumor Cell Lines

The influence of Kevetrin on the viability of 10 different types of human tumor cells, including carcinomas of the lung, colon, breast, ovary, prostate, sarcomas, gliomas and leukemias was determined using the Cell Proliferation Assay described above Cellular viability was measured after continuous exposure to Kevetrin for three doubling times The indicated concentrations of Kevetrin correspond to the average IC ₅₀ S The results are set forth below Generally, Kevetrin has potent activity toward human tumor cells of epithelial origin The cytotoxic effect of Kevetrin was most pronounced toward non-small cell lung, colon and ovarian carcinomas with IC ₅₀ S ranging from 11 to 68 ng/ml Interestingly, Kevetrin also showed potent activity toward malignant glioma cells (IC _so s ~30 ng/ml)

C totoxicit of Kevetrin of 10 different human tumor cell lines

Time Dependence of Kevetrin Cytotoxicity

To determine the influence of exposure time on the cytotoxic effects of Kevetrin, DU-145, HCT-116, or HT-29 carcinoma cells were exposed to different concentrations of Kevetrin for 5, 10, 20, 30, or 45 minutes or 1 , 2, 6, 24, or 120 hours Clear time-dependent cytotoxic effects of Kevetrin were observed for all three cell lines with longer exposure times being associated with increased cytotoxicity The results are shown in Figure 1 The time dependence was particularly dramatic for exposure times ≤30-45 minutes In contrast, extending the drug exposure time beyond 24 hours had no influence on the cytotoxicity Activity Spectra for Kevetrin and Cisplatin

The influence of Kevetrin and cisplatin on the viability of the indicated tumor cell lines was measured using the MTT assay after continuous exposure to Kevetrin for three doubling times and the results are shown in Figure 2 The indicated values are calculated as follows log (IC ₅₀ individual cell line - IC ₅₀ average) Negative values indicate that the cell line is more sensitive than the average, whereas positive values indicate that the cell line is more resistant than the average The average IC ₅₀ S for all cell lines tested were 49 x 10 ⁷ M for Kevetrin, and 2 1 x 10 ^"6 M for cisplatin Considering the MTT assay results, comparison of the activity spectra of cisplatin and Kevetrin toward 10 different types of human tumor cells in Figure 2 shows clear differences between the two drugs The activity of Kevetrin was more marked than that of cisplatin toward lung, head and neck, breast, ovary, and colon cell lines Interestingly Kevetrin showed activity toward all head and neck, non-small cell lung, ovary, colon and glioma cell lines tested in contrast to cisplatin, which generally exhibited a more heterogeneous response within a given tumor cell type The difference between Kevetrin and the cisplatin was particularly striking for the three head and neck cancer cell lines, where Kevetrin showed activity toward all of the cell lines, whereas cisplatin was active toward one of the three cell lines Surprisingly, Kevetrin had comparatively limited activity toward leukemias, which are sensitive to alkylating agents different from what was observed for cisplatin

In vivo efficacy studies of Kevetrin in nude mice bearing human tumor xenografts Animals and Animal Care

The mice were kept on a 12 hour lιght/12 hour dark cycle with the room temperature being 18-26 ⁰ C and a relative humidity of 30-70% The food and water of the animals was given ad libitum During this acclimation period, each animal was observed at least once daily for any abnormalities or for the development of infectious disease Only animals that were determined to be suitable for use were assigned to this study Any animals considered unacceptable for use in this study were replaced with animals of similar age and weight from the same vendor When the tumor mass reached on average, around 100mm ³ , the mice were randomized and grouped according to tumor size

Human tumor cell lines MDA-MB-231 human breast carcinoma (HTB-26), HT-29 colon carcinoma (HTB-38) PC-3 prostate carcinoma (CRL-1435), HCT-15 P-glycoprotein resistant colon carcinoma were purchased from American Type Culture Collection (Rockville, MD)

The MDA-MB-231 cell line was originally isolated from the pleural effusion a 51 year old Caucasian female with breast adenocarcinoma These cells appear to be morphologically epithelial in nature The HT-29 cell line was originally isolated in 1964 from a 44 year old Caucasian female with colorectal adenocarcinoma These cells appear to be morphologically epithelial in nature

The PC-3 cell line was originally isolated from bone metastasis from a 62 year old Caucasian male with grade IV metastatic prostate adenocarcinoma These cells exhibit low acid phosphatase and testosterone-5-alpha reductase activities and appear to be morphologically epithelial in nature The HCT-15 parental cell line was originally isolated from a male with Dukes' type C colorectal adenocarcinoma These cells appear to be morphologically epithelial in nature

The A549 and NCI-H1975 multi-drug resistant human lung carcinoma lines were a gift from the Dana Farber Cancer Institute, Boston, MA

Test System The cells were cultured in 10%FBS RPMI medium The cells were obtained at passage 5 for further expansion for this efficacy study Nude mice (Nu/Nu), both male (20 to 24 g) and female (19 to 22 g), were purchased at 6 to 8 weeks old from Charles River Laboratories These mice were naive at the beginning of the study and were identified by ear punching The mice were left for five days to become acclimated to their new environment Mice were implanted with human tumor cells in a 50 50 mix of RPMI Matπgel subcutaneously in the right flank of each mouse Dosing began when tumors reached an average volume of 100mm ³

In Life Observations and Measurements The mice were observed daily for any adverse affects Mice body weights were taken prior to treatment and every other day during and post treatment If an animal became unwell, any treatment of that animal was suspended If there was no recovery, the animal was sacrificed Any animal demonstrating more than 15% weight loss was considered unwell Any animal that demonstrated a weight loss greater than 20% was sacrificed Any animals exhibiting sustained ulceration of the skin over the tumor site were sacrificed Mice tumor size measurements were taken prior to treatment and every other day during and post treatment The same scientist was responsible for taking the tumor measurements throughout the study.

Terminal Procedures

Once tumors from the vehicle group reached 1000mm ³ all animals from all the groups were sacrificed by CO ₂ asphyxiation Upon sacrifice, tumors were removed and weighed

Study Schedule

Nude mice were implanted with 5x10 ^e tumor cells in a 50 50 mix of RPMI Matπgel subcutaneously in the right flank of each mouse Dosing began when tumors reached an average volume of 100mm ³ , usually reached by day 14 post implant, and was carried out for 8 days A necropsy was performed 41 days after treatment ended

Kevetrin was prepared as described in Example 1 It was stored at ambient temperature (or <-20°C) and protected from light For administration to test animals, Kevetrin was suspended in Phosphate Buffered Saline (PBS) (sterile, at pH=74). Prior to use, the PBS was stored at ambient temperature After each suspension was prepared, it was stored at <-20°C and protected from light

Dosing

The dosing procedure began the day the mice were randomized and grouped The dose was administered, as discussed in the following paragraph, on days 7, 9 and 11 following tumor implantation Each dose was administered via the tail vein Weight loss due to Kevetrin

When Kevetrin was administered intravenously (IV) to animals bearing tumors, the weight loss due to the administration of the compound was within acceptable limits 100 mg/kg administered intravenously on days 7, 9, and 11 resulted in a weight loss of 6 8% of the body weight and 200mg/kg on the same schedule resulted in a weight loss of 9.3%. Both these concentrations may be used to establish the efficacy of Kevetrin. These results are depicted in Figure 3.

Efficacy of 200 mg/kg Kevetrin IV days 7.9,& 11 compared to 22 mq/kq Taxol IV Days 7. 9. 11 & 13 in MDA-MB-231 human breast carcinoma The animals were implanted subcutaneously with human breast carcinoma MDA-MB-231 , and the compounds were injected IV as per the schedule. Kevetrin administered animals showed greater efficacy than the Taxol treated animals. The tumor growth was delayed 12 days more than the Taxol treated animals and 32 days more than the untreated control. The results are depicted in Figure 4.

Efficacy of 200 mq/kq Kevetrin IV days 7, 9. & 11 compared to 5-FU Days 7 to 12 in HT-29 colon carcinoma.

The animals were implanted subcutaneously with human colon carcinoma HT-29, and the compounds were injected IV as per the schedule. Kevetrin administered animals showed greater efficacy than the 5- FU treated animals. The tumor growth was delayed 10 days more than the 5-FU treated animals and 33 days more than the untreated control. The results are depicted in Figure 5. Efficacy of 200 mq/kq Kevetrin IV days 7. 9, & 11 against 10 mq/kq cisplatin at on day 7 in PC-3 human prostate cancer

The animals were implanted subcutaneously with human prostate carcinoma PC-3. Kevetrin was injected IV and Cisplatin intraperitoneally (IP) as per the schedule. Kevetrin administered animals showed greater efficacy than the Cisplatin treated animals. The tumor growth was delayed 8 days more than the Cisplatin treated animals and 34 days more than the untreated control. The results are depicted in Figure 6.

Efficacy of Kevetrin 200 mq/kq days 7.9. &11 against Taxol at 22 mq/kq on days 7,9,11 & 13 in HCT-15 Human Colon Carcinoma with P-glycoprotein mediated resistance.

The animals were implanted subcutaneously with human colon carcinoma HCT-15, a P-glycoprotein resistant cell model and the compounds were injected IV as per the schedule. Taxol had little effect on such cancer, whereas Kevetrin administered animals showed efficacy in the animals. The tumor growth was delayed 15 days more than the Taxol treated and the untreated control. The results are depicted in Figure 7.

Efficacy of Kevetrin 200 mg/kq days 7,9, &11 against Taxol at 22 mg/kq on days 7,9,11 & 13 in A549 multi-drug resistant Human Lung Carcinoma. The animals were implanted subcutaneously with multi-drug resistant human lung carcinoma and the compounds were injected IV as per the schedule. Taxol had no effect on such cancer, whereas Kevetrin administered animals showed potent efficacy in the animals. The tumor growth was delayed about 26 days more than the untreated controls. The results are depicted in Figure 8. Efficacy of Kevetπn 200 mq/kq days 7.9.&11 against Taxol at 22 mq/kq on days 7,9,11 & 13 in NCI- HI 975 multi-drug resistant Human Lung Carcinoma.

The animals were implanted subcutaneously with another multi-drug resistant human lung carcinoma and the compounds were injected IV as per the schedule. Taxol had a limited effect on such cancer, whereas Kevetrin administered animals showed potent efficacy in the animals. The tumor growth was delayed about 9 days for Taxol treated animals and about 24 days more than the untreated controls The results are depicted in Figure 9.

All publications, including but not limited to books and journal articles, cited in this application are each herein incorporated by reference in their entirety. Although the invention has been described above with reference to the disclosed embodiments, those skilled in the art will readily appreciate that the specific experiments detailed are only illustrative of the invention. It should be understood that various modifications can be made without departing from the spirit of the invention. Accordingly, the invention is limited only by the following claims.