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Matches 401 - 450 out of 829

Document Document Title
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...  
JP2002511456A
(57) The method of using asymmetric epoxidation and dividing the mixture of the stereoisomeric form of a summary compound kinetically is offered. A compound has an olefin portion, one stereoisomeric form is a speed quicker than another s...  
JP2002506868A
(-- 57) summary -- a new granular チミド compound and its pharmacological tablet are offered. The compound of the present invention. Whether F and F' is R or Z defined below individually and Or are Ar which F and F' is put together an...  
JP3259191B2
PURPOSE: To obtain a compound simply and in high yield useful as an antiviral agent by reacting a specific arabinoaminooxazoline with an α- bromomethylacrylic ester and subjecting the reaction product to ring closure reaction with potas...  
JP2002504548A
(57) -OR is fragrance materials alcohol and a portion preferably guided from the third class alcohol in that case about the new ring type pro spice with which summary book invention has general formula (I). Preferably, when are used by s...  
JP2002501546A
(57) c* nucleoside is compounded by the method by which sugar is derivative-ized by a single step so that at least the summary C may be provided with heterocycle, and then heterocycle is aromatized by the further single step. In the desi...  
JP3217059B2  
JP3209796B2
PURPOSE: To provide an efficient process for continuous production of a sucrose 6-ester without requiring the addition or removal of an acid. CONSTITUTION: A soln. of sucrose and trimethyl orthoacetate in dimethylformamide is passed thro...  
JP2001192395A
To obtain an oligonucleotide having largely excessive diastereomers and containing an optically isomerically pure phosphorothioate bond, a phosphorus-bonded oligonucleotide containing substantially whole Rp bonds or whole Sp bonds, a res...  
JP2001158788A
To obtain a chiral compound suitable for producing a chloesteric liquid crystal composition.This composition uses a compound expressed by general formula I. The cholesteric liquid crystal composition is usable as cosmetics for protecting...  
JP3174410B2
PURPOSE: To obtain a sulfamate showing antispasmodic activity and useful for the treatment for symptoms such as epilepsy from an easily available source material under safe conditions. CONSTITUTION: A compd. expressed by RCH2OH (R is for...  
JP3170280B2  
JP2001139578A
To provide a medicine capable of being used as an antitumor agent owing to having excellent in vivo cytotoxicity and effect on cell periods. The subject compound is expressed by formula (I) [R1 and R2 are each a group expressed by the fo...  
JP3160105B2
PURPOSE: To provide the subject compound useful as a key production intermediate for hydantocidin known as an excellent herbicidal substance. CONSTITUTION: The compound of formula I (R1 to R4 are H or hydroxyl- protecting group; X is hyd...  

Matches 401 - 450 out of 829