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JP3371139B2 |
Fungicidal compounds having the formula (I): wherein W is CH3O.CH=CCO2CH3, CH3ON=CCONR<3>R<4> or CH3ON=CCO2CH3 and stereoisomers thereof; n is O or 1; X is oxygen or sulphur; Z is oxygen, sulphur or NR<1>; R<1> is hydrogen or alkyl optio...
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JP2002540767A |
Biologically stable inhibitors of soluble epoxide hydrolases are provided. The inhibitors can be used, for example, to selectively inhibit epoxide hydrolase in therapeutic applications such as treating inflammation, for use in affinity s...
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JP3351497B2 |
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JP2002537234A |
The present invention provides methods for producing pharmaceutical-grade particulate dithiocarbamates from secondary amines by vigorously contacting at least one secondary amine and a pharmaceutically acceptable diluent that is a solven...
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JP2002537377A |
The invention relates to a process for preparing a thiuram disulfide comprising reacting a secondary amine with carbon disulfide in the presence of oxygen and a metal catalyst in the absence of a solvent using a secondary amine of which ...
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JP2002534499A |
[Task] A compound that acts as both a surfactant and a radical polymerization initiator. Useful for emulsion polymerization of block copolymers and graft copolymers. New compound represented by the chemical formula [Chemical formula 1]: ...
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JP2002265687A |
To provide a rubber composition allowing for imparting the CR parts therefrom in contact with water with antimicrobial property and ensuring the water to be sterilized, thus affording clean and healthy living environment.This CR-based ru...
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JP3313248B2 |
PURPOSE: To produce a carbamate-substituted salicylic acid derivative having high purity in a high yield and shortened time by reacting a specific aminosalicylic acid derivative with a specific haloformate compound in the presence of a t...
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JP2002523397A |
The invention relates to novel methoximinophenylacetamides, to a process for their preparation and to their use as fungicides.
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JP3309104B2 |
Sulfonic acid stilbenes are disclosed which block the infection of cells by HSV, HIV and CMV.
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JP3306876B2 |
PURPOSE: To obtain a new carbamic acid derivative exhibiting excellent juvenile hormone-like activity to insect, exhibiting high control effect on various kinds of noxious insects, including noxious insects developed with resistance to e...
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JP2002519408A5 |
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JP2002512997A |
The present invention relates to compounds which inhibit IMPDH. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well ...
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JP2002512997A5 |
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JP3279963B2 |
To obtain a concentrated aqueous solution of ethylenebisdithiocarbamate intended to suppress crystal precipitation even at a low temperature of ≤10°C. This aqueous solution comprises 15-25 pts.wt. of calcium ethylenebisdithiocarbamate...
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JP2002512174A |
(57) [Summary] The present invention relates to a method for preparing an amino group-supporting aromatic thiol from an amino group-supporting hydroxylated compound. The present invention is also related to starting reagents, intermediat...
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JP2002511858A |
In accordance with the present invention, there are provided conjugates of nitric oxide scavengers (e.g., dithiocarbamates, or "DC") and pharmacologically active agents (e.g., NSAIDs). Invention conjugates provide a new class of pharmaco...
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JP2002511837A |
In accordance with the present invention, there is provided a new class of drugs for therapeutic treatment of such indications as cerebral stroke and other ischemia/reperfusion injury. Thus, in accordance with the present invention, dith...
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JP2002114751A |
To provide a fungicidal new derivative of phenyl(thio)urea or phenyl(thio)carbamate, to provide a method for producing the derivative, and to provide fungicidal compositions each containing such a derivative.This fungicidal new derivativ...
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JP2002088056A |
To provide an oxidation method by which a vulcanization accelerator for rubbers can be obtained in high purity and in high yield, while controlling the production of a copper salt which is a by-product.This oxidation method comprising ca...
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JP2002508409A5 |
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JP3254486B2 |
Dithiocarboxylates, and in particular, dithiocarbamates, block the induced expression of the endothelial cell surface adhesion molecule VCAM-1, and are therefor useful in the treatment of cardiovascular disease, including atherosclerosis...
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JP2001348372A |
To obtain zinc dithiocarbamate particles capable of especially readily filtering having a larger particle size and uniform size distribution.Method for producing a zinc dithiocarbamate represented by the formula [wherein R1 and R2 are de...
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JP2001526195A |
Compositions for controlling growth of plant species, and methods for using the compositions, are disclosed. The compositions contain a single-isomer enantiomeric S-benzyl thiocarbamate and are particularly useful in controlling annual w...
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JP2001328976A |
To provide a new isothiocyanatoformate derivative which is suitable as a reacting agent for the production of pyrrolotriazinone compounds, and to provide a method for producing the isothiocyanatoformate derivative in a high purity and in...
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JP3228347B2 |
PURPOSE: To provide a new cyclopropenone derivative exhibiting strong inhibiting activity to thiol protease, having excellent oral absorptivity, tissue transferability and cell permeability and expected to be useful in various uses as ph...
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JP2001302419A |
To provide an inhibitor for adhesion of a harmful underwater organism such as shellfish or the like. This inhibitor for adhesion of an organism comprises phenylthiocarbamates expressed by general formula (1) [X, Y and Z are each a 1-5C a...
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JP3222050B2 |
To obtain a peptide strongly antagonizing against endogenous GnRH, inhibiting the internal secretion of LH and FSH and the release of steroids from the gonad of mammalian and having sufficient solubility at a pH of about 5-6.5. An artifi...
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JP2001517657A5 |
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JP3199295B2 |
PURPOSE: To provide a production method for obtaining a 5-acyl-2- amidohydroquinone, forming a small amount of by-products, excellent handleability and capable of readily isolating the reaction product. CONSTITUTION: Friedel-Crafts acyla...
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JP2001192365A |
To provide an image-recording material that comprises a phenol represented by formula (I), wherein R1-R4 are each H or a substituent; L is a divalent bridge group bearing at least one methylene; X is a divalent bridge group; n represents...
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JP3189279B2 |
The invention aims at providing a device comprising lipids that act like the so-called cationic liposome and are reduced in toxicity and the lipids as the constituent of the device. The invention compounds are exemplified by 3-0-(4- dime...
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JP3180192B2 |
Salts of dithiocarbamic acid which can be converted into isothiocyanates, which are suitable intermediates for producing thiazabicyclononane derivatives and monothiourazole derivatives, in a remarkably high yield; a process for producing...
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JP2001139927A |
To obtain a new heavy metal fixing agent for fly ash comprising a thiocarbamoyl sulfide compound without eluting a toxic substance such as a heavy metal in the fly ash produced in an incineration furnace in a landfill site, and the like,...
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JP2001114737A |
To obtain a compound having excellent activities for controlling plant disease, and insecticidal and acaricidal activities. This oxime derivative is represented by the general formula [R1 is a (substituted) 1-10C alkyl; one of U and V is...
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JP3142638B2 |
PURPOSE: To obtain a material, comprising an electron donative coloring compound and an electron accepting compound containing a specific phenolic compound, capable of rapidly developing the color at low temperatures, excellent in high-s...
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JP2001500470A |
Hydroximic acid derivatives, useful as pesticides, have the formula in which G is G3 or G4 having the formula: in which R5 is lower alkyl; R6 and R7 are, independently, hydrogen or lower alkyl; W is O, S, SO or SO2; X1, X2 and X3 are, in...
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JP3120091B2 |
A method for the treatment of cardiovascular diseases and noncardiovascular inflammatory diseases that are mediated by VCAM-1 is provided that includes the removal, decrease in the concentration of, or prevention of the formation of oxid...
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JP3117780B2 |
The process according to the invention for the preparation of compounds of the formula (I) or salts thereof in which X = -O-, -O-NR<2>- or -SO2-NR<2>-, Y is N or CH, R<1> is a (substituted) alkyl, (substituted) alkenyl or (substituted) a...
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JP3118596B2 |
PURPOSE: To provide the new compound useful as an intermediate for advantageously obtaining 2-mercaptobenzaldehyde. CONSTITUTION: A compound of formula I (R is 1-4C alkyl). For example, O-o- formylphenyldimethylthiocarbamate. The compoun...
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JP2000327594A |
To separate the objective enantiomer useful in the pharmaceutical industry, chemical industry and the like, under flexible and economical conditions by reacting a specific enantiomer-contg. mixture with a specific reagent in a basic medi...
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JP2000309573A |
To obtain the subject novel 2-mercaptocarboxylic acid derivative that exhibits excellent hypoglycemic effect, hypolipidemic action and the like and is useful as a hypoglycemic agent and as a hypolipemic agent. This novel compound is repr...
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JP2000302750A |
To obtain the subject new compound usable in the immunoassay of the heterologous system of a thiocarbamate-based compound. This new compound is a compound of formula I (X is non- substituted or a halogen; R1 is a 1-5C alkyl; and (n) is 1...
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JP3086893B2 |
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JP2000511163A |
Novel N-acylsulfonamides, novel mixtures of herbicides and antidotes, and their use Safeners against phytotoxic side effects of pesticides in crop plants are compounds of the formula (I) and salts thereofwhereR1 is hydrogen, a hydrocarbo...
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JP2000510833A |
The present invention provides compounds which inhibit an envelope virus by inhibiting the fusion of the virus with the host cell. The virus may be inhibited in an infected cell, a cell susceptible of infection or a mammal in need thereof.
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JP2000510820A |
The current invention discloses hydroxyamidino derivatives useful as nitric oxide synthase inhibitors.
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JP2000510464A |
The present invention provides compounds which inhibit an envelope virus by inhibiting the fusion of the virus with the host cell. The virus may be inhibited in an infected cell, a cell susceptible of infection or a mammal in need thereof.
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JP3072127B2 |
Novel ethylene glycol compounds bearing various functional groups are used to prepare oligomeric structures. The ethylene glycol monomers can be joined via standard phosphate linkages including phosphodiester and phosphorothioate linkage...
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JP3060013B1 |
[wrap up] [Task] A selenium ion separating agent capable of effectively separating and removing a trace amount of selenium ions contained in an aqueous solution, and a method for efficiently separating and removing the selenium ions from...
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