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JP2000128893A |
To obtain a new compound useful as a spin trapping agent for scavenging nitrogen monoxide in vivo. This (S)- or (R)-hydroxyproline derivative dithiocarbamate is shown by formula I (R is H, an alkyl or the like; A is a cation) and its iro...
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JP2000103773A |
To obtain the subject new compound useful as a bactericidal agent for agriculture and horticulture.This compound is expressed by formula I [R1 is A1-CA2 or the like; A1 and A2 are each a (substituted) alkyl or the like R2 is fluoromthyl ...
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JP2000502071A |
A therapeutic system comprising: (a) a compound comprising a target cell-specific portion and a portion capable of converting a substance into another substance; and (b) a molecule capable of substantially inhibiting the conversion of sa...
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JP2000500117A |
PCT No. PCT/EP96/03639 Sec. 371 Date Feb. 18, 1998 Sec. 102(e) Date Feb. 18, 1998 PCT Filed Aug. 19, 1996 PCT Pub. No. WO97/08140 PCT Pub. Date Mar. 6, 1997N-sulfonyliminodithio compounds have the formula (I), in which R1 and R2 stand fo...
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JPH11315060A |
To provide a new electron-acceptable compound that loses its electron acceptance competence with thermal energy and is useful in the thermally sensitive recording materials. This is an electron-accepting compound that irreversibly loses ...
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JP2979022B2 |
The present invention relates to a transparent resin which has a high surface hardness and which is excellent in scratch resistance, heat resistance and chemical resistance, a glazing material, a protective cover for display devices, an ...
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JPH11511142A |
The present invention relates to the use of didepsipeptides of the general formula (I) and their salts in which the radicals have the meaning given in the description, and to new didepsipeptides and processes for their preparation.
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JPH11246581A |
To obtain a new compound imparting a marked friction-reducing effect on adding to a lubricating oil, reducing the friction coefficient even under a high temperature condition, also improving the stability of the friction coefficient and ...
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JPH11509849A |
Phenyl acetic acid derivatives of formula (I) in which: X is NOCH3, CHOCH3 and CHCH3; Y is NMR and O; R, R<1> are hydrogen and C1-4 alkyl; R<2> is hydrogen, C1-C6 alkyl, C1-C4 alkyl halide and C3-C6 cycloalkyl; R<3> is C4-C6 alkyl, subst...
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JP2901509B2 |
Acetic acid derivatives of the formula in which L, M, Q and T have the meaning stated in the description, can be used for the treatment or prophylaxis of diseases caused by the binding of adhesive proteins to blood platelets, and by aggr...
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JP2898431B2 |
A method is provided for stabilizing alkylenebisdithiocarbamates, such as 1,2-ethylenebisdithiocarbamates, (EBDC) by mixing the EBDC with formaldehyde or formaldehyde releasing agents (donor) and a co-polymerization agent which forces th...
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JP2900597B2 |
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JP2894445B2 |
The present invention provides a CETP activity inhibitor comprising as an active ingredient a compound represented by the formula (I): wherein R represents a straight chain or branched alkyl group; a straight chain or branched alkenyl gr...
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JP2891883B2 |
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JPH11503446A |
There is disclosed 3-N-substituted thiocarbamoyl-2-phenyl-1,3-propanediol carbamate, represented by the following structural formula I, that is very effective for prophylaxis and treatment of central nervous system disorders including ne...
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JP2872448B2 |
A method is provided for stabilizing alkylenebisdithiocarbamates, such as 1,2-ethylenebisdithiocarbamates (EBDC), by mixing the EBDC in the presence of water with a hydroxymethane sulfinate (HMS) which degrades to formaldehyde to reduce ...
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JP2870978B2 |
Process for the preparation of 2-mercapto-4-methyl-1,3-thiazol-5- ylacetic acid or its alkyl esters of the formula I
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JPH1160553A |
To obtain the subject compound of the E-configuration that has higher plant disease-controlling activity than the other isomer by allowing a specific chlorine-containing compound to act on the Z-isomer of a specific compound in a specifi...
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JP2858756B2 |
Fungicidal compounds of the formula (I) : and stereoisomers thereof, wherein K is oxygen or sulphur; Z is optionally substituted aryl or optionally substituted heteroaryl; X is O, S(O)n, NR<4>, CR<1>R<2>, CHR<5>, CO, CR<1>(OR<2>), C=CR<1...
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JP2845973B2 |
A polyester having dithiocarbamate group at its termini represented by the formula: wherein, in preferred embodiments, R<1> and R<2> are ethyl, The dithiocarbamate groups in the polymer can easily be dissociated upon irradiation with UV ...
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JP2846911B2 |
Compounds of formula I wherein X is oxygen or sulphur, W is CH or N, m is 0 or 1, and either a) n is 1 and Q is a non-aromatic heterocyclic ring of 3 to 10 ring atoms, containing one to three hetero atoms selected from oxygen, sulphur an...
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JPH10330725A |
To obtain an acid generator which can generate a sulfonic acid at a temperature as low as room temperature or below when stimulated by moisture by selecting a compound having a specified chemical structure. This generator has a chemical ...
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JPH10513150A |
PCT No. PCT/EP95/04522 Sec. 371 Date May 7, 1997 Sec. 102(e) Date May 7, 1997 PCT Filed Nov. 17, 1995 PCT Pub. No. WO95/29465 PCT Pub. Date Nov. 2, 1995The present invention relates to a method of synthesizing a 2-substituted nitrogen co...
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JP2836945B2 |
Dianthraquinonyl compounds of the formula where X is a radical R1, R2, R3 or R4, of which R1 is alkyl or alkenyl of at least 8 carbon atoms, R2 is -OR1 or -SR1, R3 is -NHR1 or -N(R1)2, and R4 is a group of the formula where R5 is -NHR1, ...
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JPH10512574A |
PCT No. PCT/EP96/00071 Sec. 371 Date Jul. 16, 1997 Sec. 102(e) Date Jul. 16, 1997 PCT Filed Jan. 10, 1996 PCT Pub. No. WO96/22970 PCT Pub. Date Aug. 1, 1996The invention relates to novel substituted amino acid amides, to a process for th...
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JP2829707B2 |
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JP2827938B2 |
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JPH10310570A |
To provide an aqueous solution of calcium ethylenebis(dithiocarbamate) that contains 30-50 wt.% of calcium ethylenebis(dithiocarbamate) and is stable, causing no precipitation even at a low temperature ≤0°C without complication in ope...
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JPH10310571A |
To provide an aqueous solution containing calcium ethylenebis(dithiocarbamate) and its sodium salt in a concentration of 30-50 wt.% and is stable, causing no precipitation even at a low temperature ≤10°C without complication in operat...
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JP2824049B2 |
To obtain the subject new compound useful for preparing a new antibody or its fragment. This hapten compound is a compound expressed by formula I [X is no substituent or a halogen; R1 is a 1-5C alkyl; (n) is 1-10]. e.g., 4-[N-(4- chlorob...
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JP2822625B2 |
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JPH10511676A |
There are disclosed 3-thiocarbamoyl-2-phenyl-1,3-propandiol carbamate racemate, represented by the following structural formula I: [I] and its (R)- and (S)- optical isomers and intermediates thereof, which are very effective for prophyla...
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JPH10510813A |
Novel cationic amphiphiles are provided that facilitate transport of biologically active (therapeutic) molecules into cells. The amphiphiles contain lipophilic groups derived from steroids, from mono or dialkylamines, or from alkyl or ac...
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JP2811210B2 |
The present invention relates to the use of bis(3,5-di-tertiary-butyl-4-hydroxyphenylthio)methane in treating atherosclerosis and/or hypercholesterolemia in patients suffering therefrom.
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JPH10251224A |
To obtain the subject new compound useful as an agent for alleviating hypercholesterolemia or an agent for hyperlipemia. This compound is shown by formula I [R is trifluoromethyl, phenyl, etc.; R1 is H or a lower alkyl; (1) is 0 or 1; X ...
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JPH10509185A |
Combinatorial libraries are constructed to include aminodiol monomer subunits connected by phosphodiester, phosphorothioate, or phosphoramidate linking moieties. Combinatorial libraries of the invention feature a plurality of functional ...
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JPH10235200A |
To obtain an excellent catalyst for thiourethane forming reaction providing high thiourethane forming reaction speed, being hard to generate foaming by decomposition of an isocyanate group, and to obtain a cured component excellent in cu...
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JPH10508592A |
(57) [Summary] Fluorobutenyl esters have the formula (I) and are R in the formula.1Represents hydrogen or halogen, and R2Represents one of the groups (a), (b) or (c), where V, Y, Z, R3And R5Has the meaning shown in the specification. Met...
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JPH10168055A |
To provide a method for producing a high-purity polyamine derivative by reacting a polyamine with carbon disulfide, capable of solving various problems resulting from possible formation of large quantities of by-products (e.g. hydrogen s...
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JP2767241B2 |
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JPH10130228A |
To provide an aqueous solution of potassium ethylenebis(dithiocarbamate) and its sodium salt of 30-60wt.% concentration having the stability resisting to crystallization precipitation even at a lowered temperature of 0°C to -20°C. Sodi...
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JPH10130227A |
To provide an aqueous solution of potassium ethylenebis(dithiocarbamate) of 30-60wt.% concentration which has the stability resisting to crystallization precipitation even at a lowered temperature of 0°C to -20°C. When sodium ethyleneb...
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JPH10130226A |
To provide an aqueous solution of potassium ethylenebis(dithiocarbamate) of 30-60wt.% concentration which has the stability resisting to crystallization precipitation even at a lowered temperature of 0°C to -20°C. When sodium ethyleneb...
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JPH10504799A |
Compounds of formula (I) in which X is (a) or (b), n is 0, 1, 2, 3, 4 or 5, where if n is greater than 1, the radicals R2 are identical or different; o is 0, 1, 2, 3 or 4, where if o is greater than 1, the radicals R3 are identical or di...
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JP2737717B2 |
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JP2730713B2 |
To obtain a new compound having an insecticidal activity and also controlling the shape of a noxious organism in agricultural, horticultural and forestall field. This N'-substituted N,N'-diacylhydrazine-based compound is a compound of fo...
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JPH1077261A |
To provide an aqueous dithiocarbamate solution ≥50wt.% in concentration. If this aqueous solution is an aqueous potassium dithiocarbamate solution, 50-80wt.% or higher in concentration can be accomplished. It is more preferable that th...
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JPH1076240A |
To provide a heavy metal fixing agent composed of a dialkyl dithiocarbamate aq. soln. having high chelating capacity capable of insolubilizing heavy metals by a smaller amt. as compared with a conventional product. In a heavy metal fixin...
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JPH1067732A |
To obtain a new hydrazone derivative exhibiting an exremely strong inspecticidal activity against various kinds of insect pests causing agricultural problems, relatively weak in acute toxicity to mammals, and useful as a insecticide. A h...
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JPH1067743A |
To obtain a novel compound which is useful as a synthetic intermediate for a dihydropyridine derivative used in treatment of circulatory disorder and cardiovascular functional disorder. This compound is represented by formula I [R4 is a ...
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