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Matches 601 - 650 out of 1,055

Document Document Title
JP2005514405A
A fluoroionophore for the fluorescent detection of potassium ions.  
JP2005511740A
Disclosed are substituted phenylalkynes of formula (I), wherein R1, R2, R3, R4, R5 and n are as defined, compositions containing them, and methods of making and using them to treat histamine-mediated conditions.  
JP2005511788A
A process for the preparation of [1,4,5]-oxadiazepine derivatives by reaction of N,N'-diacyl-hydrazines with 2,2'-disubstituted diethyl ethers to form 4,5-diacyl-[1,4,5]-oxadiazepines and reaction of the latter compounds with a hydrohali...  
JP3626233B2
Control of endoparasites in human beings and animals comprises admin. of cyclic depsipeptide of formula (I); R<1>,R<4> = H or opt. substd. alkyl, cycloalkyl, aralkyl, aryl, heteroaryl or heteroarylalkyl; R<2>,R<3>,R<5>,R<6> = H; 1-8C alk...  
JP2005505506A
The present invention is macrocycles of the formula (X): for treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme for the treatment of Alzheimer's disease and other dise...  
JP2005035964A
To provide a new agrochemical, especially insecticide or acaricide.The invention provides a substituted benzanilide compound expressed by general formula (1) [G is a ring such as G-7, G-13 or G-17; W1 and W2 are each independently oxygen...  
JP2004359546A
To provide a hydroxamic acid derivative useful as a prophylactic and/or a therapeutic agent for solid cancer such as cerebral tumor, esophageal cancer, stomach cancer or colon cancer.The hydroxamic acid derivative is represented by gener...  
JP3600287B2
Novel cyclic depsipeptides having 18 ring atoms, of the formula (I) in which R is hydrogen, straight-chain or branched or cyclic alkyl having up to 8 carbon atoms, and their optical isomers and racemates, and their use in controlling end...  
JP3600300B2
Prodn. of lactic-acid-contg, optically active, cyclic depsipeptides with 18 ring atoms with the aid of a Fusarium fungus or an enzyme prepn. isolated from such a fungus is new. Also claimed is the prodn. of lactic-acid-contg. optically a...  
JP2004536808A
The present invention relates to novel substituted imidates of the formula (I) in which Z, n, X, R<1 >and R<2 >have the meanings given in the disclosure, and to processes for their preparation, and to their use as pesticides.  
JP3595831B2  
JP2004534759A
Catalytic oligomerization of isocyanates comprises using a catalyst consisting of a salt in which the anion is derived from a 5-membered heterocyclic compound having at least one NH group in the ring.  
JP2004534064A
The present invention are macrocycles of the formula (IX): for treating Alzheimer's disease and other similar diseases. These compounds include inhibitors of the beta-secretase enzyme that are useful in the treatment of Alzheimer's disea...  
JP2004525111A
The invention relates to the use of crystal form (I) of the cyclic depsipeptide of the formula (I) for preparing medicaments, in particular for controlling endoparasites.  
JP3541951B2
This invention relates to dichelants, in particular compounds having two macrocyclic chelant groups linked by a bridge containing an ester or amide bond, especially compounds of formula (V) (wherein each X which may be the same or differ...  
JP2004517085A
The present invention relates to compounds of the formula Iwherein R1, R2, R3, X, Y and the dashed line are as defined in the specification, to intermediates for their preparation, to pharmaceutical compositions containing them and to th...  
JP3535217B2
PURPOSE: To provide a new compound useful as a endoparasiticide for human beings and animals, etc. CONSTITUTION: A compound of formula I [R1 and R12 are each 2-9C alkyl, 1-8C halogenoalkyl, 3-6C cycloalkyl, aryl or the like; R3-R10 are e...  
JP2004509954A
Compounds having the general formula wherein R1a, R1b, R1c, X1, X2, R2, R3, R4, R5, R6, n, Y and Z are as defined in the specification, methods of using such compounds for the treatment of diseases and pharmaceutical composition comprisi...  
JP3512412B2
PCT No. PCT/EP94/01079 Sec. 371 Date Oct. 20, 1995 Sec. 102(e) Date Oct. 20, 1995 PCT Filed Apr. 7, 1994 PCT Pub. No. WO94/25424 PCT Pub. Date Nov. 10, 1994Fullerene derivatives, methods of preparing the same and methods of using the sam...  
JP2004508377A
The present invention relates to a process for preparing fused tetrahydro-[1H]-triazoles of the formula I where the variables R, Z, Z<1>, X, W, n and Q are as defined in claim 1, by cyclization of compounds of the formula II where R is C...  
JP3506758B2
PURPOSE: To obtain a new heterocyclic compound by reacting a (2-alkyl)acryloyl isocyanate with an azomethine-based compound and facilitate treatment of the (2-alkyl)acryloyl isocyanate by dissolving the new heterocyclic compound in a sol...  
JP3505483B2
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...  
JP2004505956A
Cyclic oxyguanidine compounds, including compounds of Formulae I and II: wherein R1, R3-R6, R21-R26, L, Y, Z, and A are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhi...  
JP3499569B2
The present invention relates to novel N-substituted amino alcohols, amino acids and acid derivatives thereof in which a substituted alkyl chain forms part of the N-substituent or salts thereof, to methods for their preparation, to compo...  
JP2004503538A
Compounds of formula (I) where R5, R6a, each X, L, Cy and Lp are as defined in the specification, are tryptase inhibitors useful as antiinflammatory agents.  
JP2004502682A
The present invention is directed to hydrazino compounds that function as inhibitors of copper-containing amine oxidases commonly known as semicarbazide-sensitive amine oxidases (SSAO), including the human SSAO known as Vascular Adhesion...  
JP2004502765A
2-Alkyl-3-aryl- or -heteroaryloxaziridines are prepared in a particularly advantageous manner by oxidizing corresponding N-alkyl-aryl- or -heteroarylaldimines with an aromatic percarboxylic acid or a salt thereof in the presence of water...  
JP2004501962A
The present invention is directed to hydrazino compounds that function as inhibitors of copper-containing amine oxidases commonly known as semicarbazide-sensitive amine oxidases (SSAO), including the human SSAO known as Vascular Adhesion...  
JP3487614B2
PURPOSE: To obtain an oxadiazine deriv. which is effective in repelling harmful organisms for plants, especially breeding material of plants (such as fruits, seeds and cuttage). CONSTITUTION: This compd. is expressed by formula I or its ...  
JP3472800B2
To obtain a new alkadiyne carboxylate enabling the detection of a metallic ion through difference in color change based on solid phase polymerization reaction, and to provide a method for producing the alkadiyne carboxylate. This method ...  
JP2003313169A
To obtain a new substance useful as an insecticidal miticide for agricultural and horticultural use having high safety to mammals, and an insecticidal miticide for agricultural and horticultural use containing the new substance as an act...  
JP3462234B2
PURPOSE: To obtain a new heterocyclic compound, having excellent choline esterase inhibiting activity and antidepressant action and useful as a therapeutic or a preventing agent for senile dementia. CONSTITUTION: The compound of formula ...  
JP2003530388A
A compound having the general formula (I) and methods of using such compounds for the treatment of diseases and pharmaceutical composition comprising such compounds.  
JP2003286270A
To provide a radically polymerizable monomer forming a polymerizable product having good mechanical properties and especially suitable for the preparation of dental materials.The invention provides a specific iminooxadiazine dione deriva...  
JP2003528848A
Compounds of Formula (I), and their N-oxides and agriculturally suitable salts, are disclosed which are useful as arthropodicides wherein A is H; E is H or C1-C3 alkyl; or A and E can be taken together to form -CH2-, -CH2CH2-, -O-, -S-, ...  
JP2003528073A
The invention refers to novel propenecarboxylic acid amidoxime derivatives furthermore N-oxides and/or geometrical isomers and/or optical isomers and/or pharmaceutically suitable acid addition salts and/or quaternary derivatives thereof....  
JP3446052B2  
JP2003261410A
To use a dental material which has nonsensibility to water, consequently makes a filler content accurately correspond to demand.This dental material comprises an iminooxadiazindione derivative containing at least two free isocyanate grou...  
JP2003526635A
The invention relates to novel pyrazolyl benzyl ethers, to a process for their preparation and to their use for controlling harmful organisms.  
JP2003525213A
A method for the treatment of cancer and pain in an animal subject is disclosed, comprising administering to said animal in need of such treatment an effective amount of a compound of formula (I), wherein R<1>-R<6> are defined herein. Ph...  
JP2003524597A
A non-aqueous, particle-forming, fused pyrrolocarbazole-containing composition is disclosed. Upon contact with an aqueous medium, the particle-forming composition spontaneously disperses into suspended particles, thereby forming a stable...  
JP3419009B2
PURPOSE: To obtain a new compound having PGI2 receptor antagonistic action and useful for the prevention and treatment of thrombosis, arteriosclerosis, ischemic heart diseases, gastric ulcer, hypertension, etc. CONSTITUTION: A compound o...  
JP3408790B2
To obtain a related compound as a new fungicide. This related compound as the new fungicide is expressed by the formula. The compound and a composition comprising the compound can be used for controlling agricultural and mammalian fungal...  
JP3408791B2
To obtain a compound corresponding to a new germicidal agent. This compound corresponding to the new germicidal agent has a structure of the formula. The compound and a composition containing the compound can be used for controlling fung...  
JP3404404B2
The present invention is a fluorine-containing compound having i) a perfluoropolyoxyalkyl or -alkylene chain having an average molecular weight of 800 or more and ii) a cyclic or non-cyclic polyether atomic group. Its use as a low-scatte...  
JP3378237B2
Insecticidal dihydro-oxadiazine compounds having formula (I): wherein X is O, N or S; R is a substituted or unsubstituted phenyl or C4-C5 heterocyclic group; R<2>, R<3>, R<4>, and R<5> are one of the following: a) R<2>, R<3>, and R<4> ar...  
JP2003503397A
N-substituted perhydro-2,3-diazines of the formula Iin which the variables Z, R, m and Rare as defined in claim 1, a process for their preparation and the use of the compounds of the formula I as starting materials for preparing herbicid...  
JP2003503398A
The invention relates to substituted ureas of general formula (Ia) and (Ib), wherein variables X, Z, m, R and R have the meaning cited in claim 1 and Q represents one of radicals Q1 to Q6: (Q-1), (Q-2), (Q-3), (Q-4), (Q-5), (Q-6), wherei...  
JP2003502318A
The invention relates to cyclo-imino depsipeptides of formula (I), especially 24-membered cyclo-imino depsipeptides. The invention also relates to methods for their preparation and to their utilization in controlling endoparasites.  
JP3364205B2
To provide a new pyridazinone compound useful as a bactericide. The new pyridazinone compound expressed by formula (1) (A is -CHR-O-Z-, -CHR-S-Z-, -O-CHR-Z- or -CR=N-Z-; D is CR; Q is a heterocyclic ring-containing aromatic residue; and ...  

Matches 601 - 650 out of 1,055