| Document |
Document Title |
|
JP2007106682A |
To provide a hydrazine derivative composition having cold curability and storage stability, giving a film having excellent hardness, stain resistance, etc., and containing ≤100 ppm of monohydrazine compound, and provide a coating compo...
|
|
JP3910654B2 |
To obtain an alkoxytriazolinone useful as an intermediate for producing agrochemically active compounds such as herbicidally active compounds in a high yield. An alkoxytriazolinone of formula I (R1 is H, an alkyl or the like; R2 is an al...
|
|
JP3910652B2 |
To obtain the subject compound useful as an intermediate for producing herbicides, etc., from an inexpensive raw material in industrial scale, good yield and high purity by a new method using iminocarbonic diesters with carbazinic esters...
|
|
JP3910655B2 |
To obtain the subject compound useful as an intermediate for producing a herbicidal active compound through a reaction between a specific iminocarbonic diester and a carbazinic ester in a high yield on an industrial scale. An iminocarbon...
|
|
JP3907207B2 |
Provided is a compound of the formula: I This compound is an intermediate to and is used for preparing the arthropodicidal oxidiazine Compound II described in the specification.
|
|
JP3901945B2 |
The present invention provides non-steroidal compounds of formula I which are selective modulators (i.e., agonist and antagonists) of a steroid receptor, specifically, the glucocorticoid receptor. The present invention also provides phar...
|
|
JP2007506435A |
The invention described below relates to the discovery of the neuropeptide FF receptor subtype that mediates acute nociception and chronic neuropathic pain, compounds that selectively interact with this receptor subtype and methods for t...
|
|
JP3882195B2 |
A method for making a compound of Formula I which is racemic or enantiomerically enriched at chiral center* comprising hydrogenating a compound of Formula V in the presence of a compound of Formula VII wherein: R 1 is F, Cl, or C 1 -C 3 ...
|
|
JP3878852B2 |
A method for synthesizing hydrazodicarbonamide (HDCA) by a reaction of monohalobiuret metal salt having the formula 1 or 2, which is derived from biuret, and ammonia, wherein M is a metal and X is a halogen. The monohalobiuret metal salt...
|
|
JP2007008891A |
To provide a new hydrazinecarboxylic acid derivative capable of becoming an active ingredient for germicide for agriculture and horticulture having sufficient control effect and not giving phytotoxicity and contamination to plant bodies ...
|
|
JP2006528974A |
Novel acyl urea, thiourea, carbamate, thiocarbamate and related compounds are provided which are effective in inhibiting the cytokine-mediated inflammatory response in cultured cells, in ameliorating bone destruction in an animal model o...
|
|
JP3854865B2 |
The invention concerns a method for making aminoguanidine bicarbonate from an aqueous solution of cyanamide and an aqueous solution of hydrazine in the presence of CO2. The invention is characterised in that it consists in proceeding wit...
|
|
JP2006321770A |
To provide a new compound reactive with protons, efficiently preventing a dark reaction under relatively mild conditions such as during storage of a resist material without inhibiting a reaction of the protons with a polymer for photores...
|
|
JP3845869B2 |
This invention relates to new benzamide derivatives having a vasopressin antagonistic activity, etc. and represented by the general formula (I):wherein R1 is aryl optionally substituted with lower alkyl, etc.,R2 is lower alkyl, etc.,R3 i...
|
|
JP2006524646A |
The invention relates to ammonium salts of alpha-liponic acid of general formula (I): (Lp) (A), formed from alpha-liponic acid (Lp) and amino compounds (A)=of general formula (II) or general formula (III). The invention also relates to a...
|
|
JP3833245B2 |
This invention concerns new methods and compositions that are useful in preventing and ameliorating cachexia, the clinical syndrome of poor nutritional status and bodily wasting associated with cancer and other chronic diseases. More par...
|
|
JP2006520321A |
Provided are peptides comprising at least one azaamino acid and having beta-sheet breaking ability, useful in the treatment and prevention of diseases such as alzheimer's disease, Dementia Pugilistica (including head trauma), Hereditary ...
|
|
JP3816543B2 |
PURPOSE: To obtain an N-arylhydrazine deriv. controlling insects and mite as harmful organisms and effective in protection from damage and loss caused by the harmful organisms. CONSTITUTION: A compd. represented by formula I {A is CR4 or...
|
|
JP3801653B2 |
Hydrazine derivatives of the formulawherein Y is CO or SO2; R1 is lower alkyl, lower alkenyl, lower cycloalkyl, lower cycloalkyl-lower alkyl, aryl or aryl-lower alkyl; R2 is lower alkyl, halo-lower alkyl, aryl-lower alkyl, aryl-lower alk...
|
|
JP3779616B2 |
Compounds having the formula: wherein R is hydrogen or CO2CH(CH3)2, useful as intermediates in the preparation of the miticide bifenazate, methods for their preparation, and methods for the preparation of bifenazate.
|
|
JP2006131518A |
To obtain a new azine derivative exhibiting a high controlling effect stably at a low concentration on a wide spectrum of plant damages due to blights.The azine derivative is expressed by formula (I) [wherein, R1 is H or an alkyl; R2 is ...
|
|
JP3776153B2 |
To obtain a new 1,5-disubstituted 7a-methylperhydroinden-3a-ol having excellent affinity for Na+, K+-APase, useful for treating cardiovascular disorders. This compound is shown by formula I {a broken line is a single bond or a double bon...
|
|
JP3760431B2 |
To provide a reversible thermal recording medium having small density change at the time of repeated use without notch of the medium even in the case of repeated use with satisfactory color developability and color erasability and to pro...
|
|
JP2006503070A |
Small organic molecules capable of effecting a "pharmacological trabeculocanalotomy" in an eye by means of reducing juxtacanalicular meshwork as a barrier to outflow of aqueous. The small organic molecules increase Gelatinase A activity ...
|
|
JP2006502212A |
Use of S-adenosyl methionine decarboxylase (SAMDC) inhibitor (I) in the manufacture of a medicament for preventing or treating herpes simplex virus (HSV) infection, is new. ACTIVITY : Virucide. The antiviral activity of MGBG was detected...
|
|
JP2005537331A |
Formation of heteroatom-carbon bonds comprises reacting an aliphatic or aromatic halide with lithium, using the resulting organolithium compound to deprotonate a heteroatom, and reacting the resulting lithium salt with a carbon electroph...
|
|
JP2005307188A |
To provide a foaming preparation capable of being produced without causing agglomeration, nor with the aid of a binder, having such size distribution that primary particles are distributed in a narrow range, scarcely requiring energy for...
|
|
JP3711581B2 |
PURPOSE: To obtain a new semicarbazone derivative, having excellent insecticidal and acaricidal activities against agricultural insect pests and tetranychids in a small dose, hardly exerting adverse influences upon mammals, fishes and be...
|
|
JP3712619B2 |
The present invention provides novel cathecol hydrazone derivatives of formula (I) or pharmaceutically acceptable salts thereof, wherein R1 is C1-7 alkyl or C3-7 cycloalkyl; R2 is hydrogen, hydroxy, C1-5 alkyl or -CH2CH2C(=O)NH2; R3 and ...
|
|
JP2005263809A |
To provide a method for protecting important agronomic crops from harmful and damaging action caused by noxious organisms of insects and ticks.The N-aryl hydrazine derivative is represented by formula I [for example, 2,2-dimethyl propion...
|
|
JP3696096B2 |
To provide a compound that is suitable to use as the oxidation base and gives the strong color tone in the wide range color and also to provide a compound that has a good durability to various treatments of keratin fiber. A compound of f...
|
|
JP2005520846A |
The present invention pertains, at least in part, to novel substituted tetracycline compounds. These tetracycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms...
|
|
JP2005519114A |
Novel compounds of the formula I, in which R, R1, R2 and R3 are as defined in patent claim 1, are inhibitors of coagulation factor Xa and can be employed for the prophylaxis and/or therapy of thromboembolic diseases and for the treatment...
|
|
JP2005519113A |
The invention relates to novel aryl ketones of the formula (I) in which Z represents the groups and A1, A2, A3, R1, R2, R3, R4, R5, R6, R7, X, Y, and m are as defined in the disclosure, to their use as pesticides, in particular herbicide...
|
|
JP2005518374A |
Compounds of formula (I) or (II) wherein R1, R2, R3, R4, W, Q, G, X and Y are as defined in the specification, as well as salts, enantiomers thereof and pharmaceutical compositions including the compounds are prepared. They are useful in...
|
|
JP2005029515A |
To provide a semicarbazide curing agent capable of obtaining coating film of high alkali yellowing resistance.The semicarbazide curing agent is characterized by that 1.0 g of an aqueous solution of the curing agent with semicarbazide gro...
|
|
JP2005501121A |
Compounds of general formula (I), wherein: n represents an integer from 1 to 10; R1 and R6, independently of each other, represent a hydrogen atom, a group useful for protecting nitrogen atoms in peptide synthesis or a group of formula C...
|
|
JP3604761B2 |
PURPOSE: To obtain the diazo type recording material superior in image sharpness and storage stability by incorporating a specified 2-hydroxynaphthoic acid derivative. CONSTITUTION: The 2-hydroxynaphthoic acid derivative to be added is r...
|
|
JP3596032B2 |
|
|
JP2004339208A |
To obtain a bactericidal agent containing a new phenylhydrazine derivative as an active ingredient.This bactericidal agent contains the phenylhydrazine derivative expressed by formula [I] [wherein, X is a halogen, cyano, OH, an alkyl, an...
|
|
JP2004534779A |
The present invention is directed in part towards methods of modulating the function of protein kinases with phenol- and hydroxynaphthalene-based compounds. The methods incorporate cells that express a protein kinase. In addition, the in...
|
|
JP2004531494A |
Novel compounds of the formula I in which X, Y, Z, R, R1, R2 and R3 are as defined in Patent Claim 1 , are inhibitors of coagulation factor Xa and can be employed for the prophylaxis and/or therapy of tromboembolic diseases and for the t...
|
|
JP2004531516A |
A data processing system nested interrupt controller 24 responsive to priority level values 28, 30 associated with respective interrupt handling programs to control the execution of those interrupt handling programs. The priority level v...
|
|
JP2004531510A |
A data processing system nested interrupt controller 24 responsive to priority level values 28, 30 associated with respective interrupt handling programs to control the execution of those interrupt handling programs. The priority level v...
|
|
JP3555021B2 |
To obtain a semicarbazide derivative that shows high compatibility to polycarbonyl compound and is useful as a curing agent for polycarbonyl compound by allowing a specific polyisocyanate to react with hydrazine or the like. A urethane t...
|
|
JP2004224771A |
To provide a method for synthesizing 1,1,5,5-tetraalkylcarbohydrazides in a simple method by using an inexpensive material having a low toxicity.This method for synthesizing the 1,1,5,5-tetraalkylcarbohydrazides is provided by performing...
|
|
JP2004523490A |
The present invention relates to novel, non-peptidic small organic compounds having an affinity for cyclophilin (CyP)-type immunophilin proteins. In the compounds of this invention, at least two carbo- or heterocyclic groups are attached...
|
|
JP2004161670A |
To provide a compound and an insecticide comprising the same as the active ingredient exhibiting high insecticidal effect and a broad insecticidal spectrum on agricultural/horticultural insect pests but no harm to useful crops at all.The...
|
|
JP2004161692A |
To provide a method for easily and efficiently producing a hydrazodicarbonamide at a low cost.The method for producing the hydrazodicarbonamide involves reacting a halo-biuret compound represented by general formula (1) [wherein, X is a ...
|
|
JP2004149413A |
To provide a novel hydrazone derivative useful for controlling pests or its salt or an intermediate therefor and to provide a method for producing the hydrazone derivative or its salt.The hydrazone derivative is represented by formula [I...
|
