Login| Sign Up| Help| Contact|

Patent Searching and Data


Matches 851 - 900 out of 1,362

Document Document Title
JP3153260B2  
JP2001072678A
To obtain a new oxadiazine derivative useful for controlling insects. A compound of formula I (A is an aromatic or heterocyclic group; R is H, a 1 to 6C alkyl or the like; X is N-NO2 or N-CN), for example, 3-methyl-4-nitroiminoperhydro-1...  
JP2001502677A
(57) A shows アルカジイル and summary book invention shows アリール or the ヘテロア reel by which Ar can be replaced by the case, respectively, Alkane ジイル for which G can be interrupted by double 素原子 by the sing...  
JP2001048869A
To readily and environmentally-friendly produce an oxaziridine compound useful as a raw material for various organic synthesis at a low cost by reacting a cycloalkanone with ammonia, and oxidizing the product. A cycloalkanone (e.g. cyclo...  
JP2001502297A
(57) Summary book invention offers the new crypto フィシン compound which can be used as an anti-new organism medicine for the medical treatment of the cancer as an antifungal agent, in order to collapse a microtubule system. Further...  
JP2001048868A
To provide a method for readily and environmentally-friendly producing 3,3-alkyleneoxaziridine in high yield. A cycloalkanone is reacted with ammonia and hydrogen peroxide, and the product is reacted with a carboxylic acid and/or a carbo...  
JP2001502298A
(57) Summary book invention offers the intermediate field and the method of a crypto フィシン compound group useful to manufacture.  
JP3135659B2
PURPOSE: To simply obtain perfluoro-oxyaziridines in high yield which are useful in the preparation of perfluoroaminoether polymers, nitrones, etc., by reacting a specific perfluoroimine with an aromatic peroxyacid in an aprotic solvent ...  
JP3135660B2
PURPOSE: To obtain the compound useful as raw materials for polymers with excellent chemical inactivity and thermal stability by specific perfluoroimine and perfluoroalkyl-fluoroformyl peroxides to react with each other. CONSTITUTION: Pe...  
JP2001501916A
(57) the オキサジ azine of summary type (I) (the inside of a formula and R are F, Cl, or full オルアルコキシ, and R is アルキル), It is manufactured by making it react to ジアルコキシ methane under existence of a pro...  
JP3132167B2
PURPOSE: To obtain a depsipeptide derivative having anthelmintic action at a low cost in high yield by carrying out the polycondensation of a condensation product of an amino acid and an α-chloropropionic acid ester and subjecting the p...  
JP2001500853A
(57) Summary book invention offers the new crypto フィシン compound which can be used as an anti-new organism medicine for the medical treatment of cancer, in order to collapse a microtubule system. The present invention offers the t...  
JP2001500496A
(57) Summary book invention offers the production method of a crypto フィシン compound pure in diastereomer.  
JP2001500484A
(57) Summary book invention provides the manufacturing process and manufacturing process of a crypto フィシン compound with useful new intermediate field.  
JP2001500128A
(57) Summary book invention offers the method of manufacturing a new crypto フィシン compound and a crypto フィシン compound.  
JP3121355B2  
JP2000352806A
To provide a processing solution for a silver halide photographic sensitive material having rapid desilvering performance, not causing the stain of an edge part and excellent in liquid preservation stability and environmental suitability...  
JP2000516596A
(57) Summary book invention relates to a useful new compound to prevention and prevention of the pathology of cell adhesion and cell adhesion mediation nature. The present invention relates to the method of using these compounds again to...  
JP2000319249A
To obtain a new compound useful as a medicine for treating or preventing virus infection, especially cytomegalovirus infection. A compound of formula I [R1 is H, a (substituted) 6 to 10C aryl, (five to ten-membered aromatic heterogeneous...  
JP2000302770A
To provide a novel compound that has the antagonism to 2-amino-3- hydroxy-5-methyl-4-isoxazolepropionic acid receptor and is useful for prevention, treatment and amelioration of neurodegenerative diseases, for example, cerebral ischemia,...  
JP2000302676A
To obtain a medicinal composition capable of protecting and preventing a mitochondoria genome and/or mitochondoria from being damaged by including a specific hydroximic acid derivative as an active ingredient. This medicinal composition ...  
JP3104142B2
PURPOSE: To obtain a new benzamide derivative useful as a therapeutic agent for digestive system diseases, having accentuating action on function of digestive tubes and anti-vomiting action. CONSTITUTION: A compound of formula I (R1 is H...  
JP2000290268A
To selectively obtain a polyisocyanate having excellent reactivity and high compatibility with polyols and solvents, etc., by reacting a polycyclic aliphatic polyisocyanate with carbon dioxide gas using a specific t-phosphine. A polyisoc...  
JP2000290269A
To selectively obtain a polyisocyanate having excellent reactivity and high compatibility with polyols and solvents, etc., by reacting a polycyclic aliphatic polyisocyanate with carbon dioxide gas using a specific pyridine compound. A po...  
JP2000248043A
To obtain a polyisocyanate composition excellent in reactivity at low temperature, also good in preservation stability and useful as a raw material for various kinds of polyurethanes by including a specific diisocyanate and a specified p...  
JP2000511895A
(57) [Abstract] The present invention is known as an initial output for manufacturing the compound which has sterilization and the Killing mold characteristic (the [ international publication ] No. 95/04728 specification), It is related ...  
JP2000248045A
To obtain a polyisocyanate composition excellent in reactivity at low temperature, also good in preservation stability, and useful as a raw material for various polyurethanes by including a specific diisocyanate and a specified polyisocy...  
JP2000510820A
(57) Summary book invention indicates a water oxidization アミジノ derivative useful as nitric oxide sinter zein ヒビター.  
JP2000508630A
(57) Summary book invention about new (1, 3, 4) * オキサ diazine derivative of formula (I), Inside of a formula: R and R become independent mutually and Hydrogen or アルキル which can be replaced with halogen by the case, respecti...  
JP3061863B2  
JP2000507805A
(57) The production method of the crypto フィシン compound by summary bacteria fermentation is indicated with the new composite manufactured by it.  
JP2000505473A
(57) Summary book invention offers the new crypto フィシン compound which is useful to the destruction of a microtubule system for dealing with the cancer as antineoplastic agents, and possible in it. The present invention offers the...  
JP2000504321A
(57) Among summary type (I) and a formula, A expresses alkane ジイル which may be replaced by the case if needed, and;R Cycloalkyl, Express アリール or ベンゾ condensation hetero シクリル, ;E by which each of this basis may...  
JP2000086640A5  
JP2000086640A
To provide a method for producing a product having imino- oxadiazinedione group, whose content is improved in a trimer mixture, without need of handling hydrofluoric acid in the production of a catalyst. This method comprises subjecting ...  
JP2000503679A
(57) R among the compound type of summary type (I) The formula G, G, and G, G, It is a basis of G, G, or G, and;Y is the hetero (C*C) アルキル bridge which may be replaced, This is those use in the intermediate field for manufacturin...  
JP2000502351A
(57) Summary book invention offers the new crypto フィシン compound for the disposal of the cancer as antineoplastic agents which it is useful and is obtained, in order to destroy a microtubule system. The present invention offers th...  
JP3014146B2  
JP2000502050A
(57) Summary book invention relates to the macro amphiphilic molecule which checks production of the metalaw proteinase and the tumor necrosis factor (TNF) which include アグレカナーゼ. Especially these compounds are inhibitor of ...  
JP2000053663A
To provide a novel compound that has antimycotic activity against Candida albicans or the like and is useful as an effective and safe antimycotic agent. The objective compound is represented by the formula. The compound of the formula is...  
JP3011955B2  
JP2000500984A
(57). Summary book invention is based on the enzyme tablet isolated from the fungus stock of eye a non-spore imperfect bacillus (Agonomycetales), or them. It is related with the new production method of the substitution アリール lact...  
JP2000034284A
To provide a production process for a trimerized polyisocyanate in the presence of a quaternary phosphonium polyfluoride trimerization catalyst where the trimetized polyisocyanate product bears iminoxazinedione groups in an amount of at ...  
JP2000501067A
(57) Summary book invention offers the new crypto フィシン compound which has that it is useful for the reason of the medical treatment of cancer as an antifungal as an anti-new organism agent for collapse of a microtubule system. Th...  
JP2000034284A5  
JP3003940B2  
JP2000500131A
(57) The "acid * amide" calyx arene of formula (I) below a summary is indicated. L is *CH* or *O*CH*O*, and here and L, Between each aryl group, it may be the same, or may differ and R, Even when it is H, halogen or a fatty series hydroc...  
JPH11322728A
To obtain a heterocyclic compound useful for physiologically active substances such as agrochemicals and drugs under mild conditions with ease in a high yield, by applying an amide compound as a starting substance. An amide compound of f...  
JPH11322593A
To obtain an anticancer agent having an inhibitory activity of the propagation of cancer cells and an inhibitory activity of tubuline by including a specific acetamide derivative. This anticancer agent and tubuline inhibitor contain usua...  
JPH11255757A
To obtain the subject new compound having crown ether structure, high in ion transfer ability, capable of solid phase polymerization, and useful as a raw material for functional materials such as electroconductive materials, electrode ma...  

Matches 851 - 900 out of 1,362