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Matches 401 - 450 out of 854

Document Document Title
JP2005526852A
[化 1] The present invention aims at the pharmaceutical composite containing the manufacturing process of the new compound of formula (I) which is as X, R, R, R, R, R, and R having written in the specification, and this derivative, and ...  
JP3662954B2
PURPOSE: To obtain the subject compound, useful for a raw material, etc., for liquid crystals, medicines, agrochemicals, etc., by optically resolving a recemic 1-benzyloxy-6,6,6-trifluoro-4-hexyn-3-ol, then carrying out the reduction of ...  
JPWO2003072587A1
本出願には、システイン若しくは/およびシ ステイニルグリシンまたはシスチンと還元糖 とを水性溶媒中に加熱下に保持することを特 徴とする不揮発性チアゾリジン化合物の...  
JP2005514352A
The present invention relates to the cure for the autoimmune disease characterized by X, R, R, R, R, and R including the remedially effective thing to do for quantity medication for the compound of: which is as giving a definition in thi...  
JP2005509615A
The compound of a new carbohydrate base with an attached ring system which has antibacterial properties or cell-growth control activity. Humans and an animal are medicated with this compound for bacteria, a fungus, a virus, protozoan inf...  
JP3621097B2  
JP2005503358A
The present invention includes the cure for HIV and HBV including medication of the compound of beta* halo nucleoside, a composite and the above-mentioned compound, or a composite, or abnormal cell multiplication.  
JP2004537533A
The present invention relates to the method for the protection of an optic nerve cell using the optic nerve cytoprotective agent and this スルファ mate derivative which are characterized by containing the スルファ mate derivative...  
JP3602050B2  
JP2004262911A
To provide a method for producing effectively an optically active α-aminoketone.A method for producing an optically active α-aminoketone shown by general formula (2) comprises allowing a new chiral alkoxide originating from glucose, wh...  
JPWO2002096921A1
本発明はアポトーシスを誘導する新規なグル コース誘導体およびその医薬としての使用に 関する。本発明のグルコース誘導体は、次一 般式(I)[式中、X、Y、Zは同一ま...  
JP2004526984A
(a) As the compound hardened in an action of acid or the compound; which the solubility increases in an action of acid, and a (b) photosensitivity acid donor, R among (Ia), (Ib), (Ic), (IIa), (IIb), or (IIc) [type, For example, C*C ア...  
JP2004222682A
To provide tea leaves with reduced caffeine content, capable of being taken by a large amount for a long time as an antiallergic beverage or food.A method for producing tea leaves is provided by immersing any of raw leaves of "Benifuuki"...  
JP2004523478A
the indri ロピロロ carbazole compound of the present invention is new -- it is related with a medicine tablet useful although the トポイソメラーゼ *I activity of N12, an N13* bridged sugar derivative, and this derivative is s...  
JP2004182664A
To provide a method for efficiently and safely carrying out fluorination of saccharide in high selectivity.The specific part of saccharide can selectively and simply be fluorinated without having influence on the protective groups by rea...  
JP2004518803A
The present invention relates to use of the above-mentioned compound in manufacture of a red-throated loon Lamaism イシン derivative, genetic engineering, its production method that used biosynthesis, the medicine containing the above...  
JP2004175792A
To provide a method for simply producing a 2,2'-anhydro-1-(β-D-arabinofuranosyl)uracil compound at a low cost.This method for producing the 2,2'-anhydro-1-(β-D-arabinofuranosyl)uracil compound comprises heating a 3',5'-O-sulfinylxylour...  
JP2004517932A
The present invention relates to the tablet of a medicine compound. The present invention provides details with the manufacture methods of the composite which is prepared from a boronic acid compound and which it is stable and can be per...  
JP2004517931A
The present invention offers the stable compound prepared from the boronic acid of a formula (1) and (Z and Z being portions of sugar origin among a formula), and its freeze-drying compound. The present invention offers the manufacture m...  
JP2004123605A
To provide a method for highly selectively, efficiently and safely advancing the fluorination reaction of a desired substrate.This fluorination method comprises reacting a specific fluorine compound such as N, N-diethyl-α, α-difluoro-(...  
JP2004510700A
Although development of symptoms of II type diabetes and X syndrome is prevented, the useful 鎮痙 agent derivative is indicated.  
JP3516959B2  
JP2004505004A
The inside of the formula (I) : [化 1] type for dropping the blood pressure in [grow / too much / fat / especially] an individual, X is CH or oxygen, ; R is hydrogen or アルキル, and; and R, R, R, and R are hydrogen or アルキル ...  
JP2003530300A
(57) -- A summary formula I: (the inside of a formula and X are CH or oxygen, and;R is hydrogen or アルキル --; and R --) for maintaining a weight fallR, R, and R are hydrogen or アルキル independently, and when X is CH, R and R ...  
JP2003527324A
(57) -- summary type (I) -- the heterocyclic aromatic amide (HAA) according to 化 1 this specification defines X*X, M, Z, and A among a formula]. The present invention includes the water ghost, the salt, and the complex of that again. T...  
JP2003212892A
To provide a lactosamine derivative also useful as an intermediate for synthesis of various kinds of oligosaccharides, and to provide a method for efficiently producing the lactosamine derivative.This new lactosamine derivative is repres...  
JP3430318B2
PURPOSE: To provide halistatin 1 which is useful as a material for anticancer drugs. CONSTITUTION: Halistatin 1 is shown by the formula. This compound is obtained from the sponge Phkellia-carteri gathered in the west Indian Ocean by extr...  
JP3430317B2
PURPOSE: To provide halistatin 2 which exerts, as an anti-tumor agent, a particularly excellent activity against leukemia, small cell carcinoma of lung, large bowel cancer, CNS cancer and melanoma. CONSTITUTION: The halistatin 2 is shown...  
JP2003176250A
To provide a method of synthesizing phosphine oxide being a synthon for ring A used for preparing 19-nor-vitamin D compound and provide a new synthetic intermediate that is formed on the way of the synthetic route.In this new synthetic p...  
JP3411280B2  
JP3403218B2
PURPOSE: To provide a new compound useful as an antiliphemic and for treating liver disorders with cholestasis with no side-effects, which has activity to decrease the cholesterol level in the serum and has high affinity for transport sy...  
JP2003055394A
To provide a synthetic compound which is useful for obtaining an oligo saccharide specifically bound to a target nucleic acid in the specific sequence of a gene, and to enable the enhancement in the effect of an anti-gene method. This di...  
JP2003505465A
(57) the anti-convulsiveness compound of 、 which is as having defined X, R, R, R, R, R, and R in this specification among the summary general formula (I) : 化 1 type, It is useful to dealing with neurodegenerative which happens betwee...  
JP2003502325A
(57) summary book invention, It is related with the abstraction method of a Sis *8* Ben Jill *7, 9* オキソ*2, and 8* アザビ cyclo 4.3. 0 nonane (or it is also called below Sis *6* Ben Jill *5 and 7* オキソオクタヒドロピ...  
JP2003012683A
To provide a simple method for the production of a sugar oxazoline derivative.The sugar oxazoline derivative expressed by general formula (2) (R1 is H or (CH2)n-CH3 ((n) is 0-5); R2, R3, R4, R5 and R6 are each independently H, N3, protec...  
JP2002544135A
(-- 57) summary -- the convenient large-scale manufacture synthetic method of D* elytrous fin ゴシン of high isomeric purity and セラミド is explained. 化 1  
JP2002543214A
(57) Summary subject book invention offers the oligonucleotides containing new LNA nucleoside analogs (L* リボ *LNA (s)) and an L* リボ *LNA nucleoside analog. A solution means -- the oligomer containing at least one nucleoside analo...  
JP3356324B2  
JP2002537264A
(57) Summary book invention relates to a benzaldehyde derivative useful as an antineoplastic drug. The thing with the compound of the present invention is new in itself.  
JP2002537263A
(57) Summary book invention relates to a benzaldehyde derivative useful as a medicine which can be used in order to prevent or treat the disease and/or autoimmune disease which are produced by the antineoplastic drug, the antivirotic, an...  
JP2002536328A
(57) Anticonvulsant derivative useful to the disposal of summary autism.  
JP2002535270A
(57) A useful anti-convulsiveness derivative is indicated in the disposal of a summary cluster headache.  
JP2002534529A
(57) Summary book invention relates to a series of new substitution pentose and hexose monosaccharide derivatives. This shows a leading cell adhesion prevention action and an antiinflammatory effect. The production method, the medical tr...  
JP2002534530A
(57) -- summary book invention -- general -- 2* -- it is related with the compound and process of the formula I for compounding the derivative of 3** iso pro ピリデン * alpha*L * キシロ *2* ヘキスウロフラノソン acid. The...  
JP2002293792A
To provide a low-cost, safe and industrially excellent method for producing a nucleoside or sugar derivative in which a secondary hydroxy group is substituted with fluorine, in which the fluorination can be carried out by one process.A n...  
JP2002533468A
(57) Summary book invention is general formula I: 化 1 (R each among a formula). Become independent and Hydrogen, the alkyl group アルキル (ed) or replaced, the acyl group アシル (ed) or replaced, Are chosen from a phosphate grou...  
JP2002241390A
To provide a new efficient synthesis method for industrially producing an L-type nucleic acid derivative as a medicine.A method by which the L-type nucleic acid derivative can industrially be produced from L-arabinose, one of few industr...  
JP2002235096A
To provide a method for using a cyclic sugar ketone as a catalyst for a peroxo compound.A method for using a cyclic sugar ketone of formula (1) (wherein, R1 and R2 are each H, a 1-22C alkyl, a 2-22C alkenyl or phenyl; R3 is a 1-4C alkoxy...  
JP2002201372A
To provide a new pigment of a rose flower.This new pigment compound is represented by the general formula I such as formula 20, and a rose plant enhanced in the pigment is provided.  
JP2002517504A
(57) Summary book invention offers the new method for compounding M6G, and the intermediate field for it. In order to compound M6G, since the conventional method generates alpha* anomer, the essential problem which should be conquered is...  

Matches 401 - 450 out of 854