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Matches 451 - 500 out of 864

Document Document Title
JP3356324B2
Compounds of the general formula (I): wherein R1, R2, R3, R4, R5, R6, n and p are as herein defined; exhibit anticonvulsant activity and are thus useful in the treatment of conditions such as epilepsy. Compounds of this class are also us...  
JP2002537264A
The present invention relates to benzaldehyde derivatives which are useful as anticancer agents. Some of the compounds of this invention are novel per se.  
JP2002537263A
The present invention relates to benzaldehyde derivatives which are useful as anticancer agents. Some of the compounds of this invention are novel per se.  
JP2002536328A
Anticonvulsant derivatives useful in treating autism.  
JP2002535270A
Anticonvulsant derivatives useful in treating cluster headaches are disclosed.  
JP2002534529A
The present application relates to a group of novel substituted pentose and hexose monosaccharide derivatives, not previously disclosed, which exhibit potent anti-cell adhesion and anti-inflammatory activities. Methods of preparation, ph...  
JP2002534530A
This invention relates generally to compounds and processes for synthesizing derivatives of 2-3-O-isopropylidene-alpha-L-xylo-2-hexulofuranosonic acid. The compounds of this invention are useful, inter-alia, for the inhibition and preven...  
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
The application relates to the design and synthesis of novel hexasaccharides of general formula (I), wherein: each R is independently selected from hydrogen, an alkyl or substituted alkyl group, an acyl or substituted acyl group, a phosp...  
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
The invention provides a novel method for synthesizing Morphine-6-Glucuronide comprising the step of reacting 3-O-pivaloyloxymorphine and methyl 1alpha,2-ethylorthopivalate-3,4-di-O-pivaloylglucouronate.  
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
Novel granulatimide compounds and pharmaceutical formulations thereof are provided. Compounds of this invention have general formula (I) or (II) wherein are independently R or Z as defined below, or in combination F and F' is Ar1 as defi...  
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
C-nucleosides are synthesized by a method in which a sugar is derivatized in a single step to provide a heterocycle at the C1 position, and then the heterocycle is aromatized in another single step. In one class of preferred embodiments ...  
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...  
JP2001502316A
(57) The compound and method for manufacturing the EPO キシド on a エナンチオマー selection target from an olefin using summary chiral ketone and an oxidizer.  
JP2001501580A
This invention pertains to nucleoside analogs that have antiviral activity and improved metabolic stability, compositions comprising them, and methods of antiviral treatment employing them. More particularly, this invention pertains to i...  
JP2001501643A
The present invention describes a method for treating neuropathic pain comprising administering to a mammal afflicted with such condition a therapeutically effective amount for treating such condition of a compound of formula (I), wherei...  
JP2000514796A
Anticonvulsant derivatives useful in treating psoriasis are disclosed. 00000  
JP2000514425A
A method for treating obesity comprising administering a therapeutically effective amount of a compound of the formula: is disclosed.  
JP2000302740A
To provide a method for producing an organic azide, giving an azide functional group to an organic compound in a high yield, by adding an alkyl carboxylic acid ester having a boiling point above the reaction temperature in a nearly equim...  
JP2000514426A
Disclosed herein is a method of treating amyotrophic lateral sclerosis with topiramate and related compounds.  
JP3080973B2
This invention provides novel cyclic acetals useful as delayed release flavorants and odorants. These compounds possess no detectable flavor or odor themselves at normal temperatures and atmospheric conditions but release an aldehyde fla...  
JP2000509364A
The present invention relates to compositions and methods for inhibiting the aging of amino-containing amino acid, peptides, proteins and biomolecules. Accordingly, a composition is disclosed which comprises an agent or compound capable ...  
JP3046359B2
The present invention relates to D-pentofuranose derivatives represented by the following formulas (1) through (4): (wherein A represents a chlorobenzoyl group; R<1> represents a hydrogen atom, an aliphatic lower acyl group, a substitute...  
JP3044175B2
PURPOSE: To remove an allyl group, etc., in high selectivity and high yield without exercising bad influence on other functional group by reacting a specific compound containing an allyl group, etc., with a sulfinic acid compound in the ...  
JP2000502888A
(57) Summary book invention offers the reagent for using it for トピラ mate immunity analysis and this immunity analysis. Especially a トピラ mate, In order to use it as the sign guided and coupled directly by a トピラ mate's ...  
JP3012924B2  
JPH11511480A
Methods and intermediates for the preparation of oligomers containing diastereomerically enriched phosphorothioate linkages are disclosed.  
JPH11246588A
To obtain the subject new oxazoline derivative useful as a plant elicitor, humectant, etc., by reacting di-N-acetylchitobiose-hexaacetate with acetyl chloride and a base and then, enzymatically deacetylating the resultant product. This n...  
JP2938193B2
The present invention relates to an efficient new route for the preparation of (+)-nojirimycin and (+)-1-deoxynojirimycin which involves the steroselective reductive amination of 1,2-O-isopropylidene-5-oxo- alpha -D-glucuronolactone. The...  
JP2930983B2
A trehalose derivative of the formula: wherein one, two, three or four of R<1>, R<2>, R<3>, R<4>, R<5>, R<6>, R<7> and R<8> are independently selected from the group consisting of C1-40 aliphatic acyl groups and all the rest of them are ...  
JPH11508549A
PCT No. PCT/FR96/00991 Sec. 371 Date Jan. 29, 1999 Sec. 102(e) Date Jan. 29, 1997 PCT Filed Jun. 25, 1996 PCT Pub. No. WO97/01343 PCT Pub. Date Jan. 16, 1997This invention relates to a new use of a sophorolipidic compound, of pharmaceuti...  
JPH11504623A
Esters of hydroxyl-containing indolocarbazoles and acids containing selected solubilizing groups are provided. Compositions including the indolocarbazole esters and methods for the use of the indolocarbazole esters are also provided.  
JP2843592B2
A process of preparing l -biopterin is disclosed which comprises the steps of: Subjecting to selective Grignard reaction D-ribose having the hydroxyl groups in the 2- and 3-positions protected by an acetal group to give 6-deoxy-3,4-O-alk...  
JPH10251263A
To obtain the subject compound in a high yield by an industrially easy method comprising oxidizing trehalose, hydrolyzing the oxidized trehalose and subsequently collecting the material from the hydrolysis product. This method for produc...  
JP2787344B2
5-Amino-5-deoxy-1,2-O-isopropylidene- alpha -D-glucofuranose is conveniently prepared by a hydride reduction of 5-azido-5-deoxy-1,2-O-isopropylidene- alpha -D-glucuronolactone and can readily be converted to nojirimycin, deoxynojirimycin...  
JPH10507782A
A method for vacuum distillation includes separation of a liquid product delivered to a reservoir under vacuum into a vapour-gaseous phase and at least one liquid fraction, withdrawal of the vapour-gaseous phase from the reservoir using ...  
JP2770892B2
PURPOSE: To provide the subject new derivative enabling accurate and efficient determination of α-amylase activity and useful as a reagent for the determination of α-amylase activity. CONSTITUTION: The derivative of formula I (X1 is me...  

Matches 451 - 500 out of 864