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Patent No. 5273766

Tenderizing Meat

A method to tenderize meat with an explosive shockwave.

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Class 564/150 - Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)


Subclass of Class 564 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein the carboxylic acid residue contains hydroxy
No. of patents: 113
Last issue date: 07/15/2008


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NumberTitleIssue Date
7399788N-deacetylthiocolchicine derivatives, their use and pharmaceutical formulations containing them
Disclosed is a series of N-deacetylthiocolchicine derivatives of formula (I) in which: the linker is a bivalent straight or branched C1-C8 alkyl residue, C3-C8 cycloalkyl, a phenylene or heterocyclic C4-C6 ...
07/15/2008
7317125Diacylglycerol acyltransferase inhibitors
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutica...
01/08/2008
7304161Diaclhydrazine ligands for modulating the expression of exogenous genes in mammalian systems via an ecdysone receptor complex
The present invention relates to non-steroidal ligands for use in nuclear receptor-based inducible gene expression system, and a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding dom...
12/04/2007
7220870Hydrolytic kinetic resolution of cyclic substrates
The present invention relates to a process for stereoselective or regioselective chemical synthesis which generally comprises reacting a nucleophile and a chiral or prochiral cyclic substrate in the presence of a non-racemic, chiral catalyst to produce a stereoisome...
05/22/2007
7189873Propargylether derivatives, a process for their preparation and their use for controlling phytopathogenic microorganisms
The invention relates to 4-propargyloxy-benzyl dervatives of the general formula (I) including the optical isomers thereof and mixtures of such isomers, wherein R1 is hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl or optionally ...
03/13/2007
7173063Topoisomerase poisons for the treatment of proliferative disorders
Methods for the treatment of a proliferative disorder are provided in which a subject in need of such treatment is administered an effective amount of a compound selected from: compounds of formula (I) or a pharmaceutically acceptable salt thereof, wherein X1
02/06/2007
7034015Aminobenzoephenones
The invention relates to a novel class of aminobenzophenones derivatives, to pharmaceutical preparations comprising said compounds, to dosage units of such preparations, to methods of treating patients comprising administering said compounds, and to the use of said ...
04/25/2006
6706765Aminoguanidines and alkoxyguanidines as protease inhibitors
Aminoguanidine and alkoxyguanidine compounds, including compounds of the formula: wherein X is O or NR9 and R1-R4, R6-R9, R11, R12, Ra
03/16/2004
6518310Aminoguanidines and alkoxyguanidines as protease inhibitors
Aminoguanidine and alkoxyguanidine compounds, including compounds of the formula: ##STR1## wherein X is O or NR9 and R1 -R4, R6 -R9, R11, R12, Ra, Rb, R
02/11/2003
6455515Salicylohydrazide derivatives, processes and intermediates for their preparation, compositions comprising them, and their use
Salicylohydrazide derivatives of the formula I ##STR1## in which the index and the substituents have the following meanings: X is halogen, NO2, cyano, alkyl or alkoxy; m is 0, 1, 2 or 3, it being possible for the substituents X to differ from each o...
09/24/2002
6207862Precursors for the production of chiral 1,3-aminoalcohols
The disclosure describes novel precursors for the preparation of chiral 1,3-aminoalcohols. The precursors are chiral 4-hydroxycarboxamides, 4-hydroxyhydroxamic acids, or 4-hydroxyhydrazides produced from chiral gamma-lactones, which in turn are derived fr...
03/27/2001
6172108Hydrazide compounds
Compounds of formula (I): R--NH--A--CO--NH--NH--(W)n --Z (I) wherein: n is 0 or 1, W represents --CO-- or S(O)r wherein r is 0, 1 or 2, Z represents a group selected from aryl, arylalkyl, heteroaryl and heteroarylalkyl, each optionally substi...
01/09/2001
6166257Asymmetric hydrogenation method of a ketonic compound and derivative
The present invention relates to a process for the asymmetric hydrogenation of a ketonic compound and derivative. The invention relates to the use of optically active metal complexes as catalysts for the asymmetric hydrogenation of a ketonic compound and ...
12/26/2000
6124356Fungicides
A fungicidal compound of formula (I): or a stereoisomer thereof, wherein A is CH or N, B is OCH3 or NHCH3, E is --NR1 --C(CH3).dbd.N-- or --N.dbd.C(CH3)--NR1 --, R1 is H, C1...
09/26/2000
6096890Process for substituted hydrazides using carboxylic acids
This invention provides a convenient process for the preparation of monoacylhydrazines from carboxylic acids or their salts and hydrazine or substituted hydrazine in the presence of a 1,3,5-triazine substituted with at least one chloro or fluoro. The resu...
08/01/2000
6046330Complexes of ultraviolet absorbers and quaternary ammonium compounds which are substantially free from unwanted salts
This invention relates to complexes of ultraviolet absorbers with quaternary ammonium compounds which are substantially free from unwanted salts. Such complexes are formed through ionic bonds formed between the two compounds. The inventive complexes are t...
04/04/2000
6043282Azinooximethers, processes and intermediate products for manufacturing same, and the uses thereof in combating harmful fungi and pests
Azinooxime ethers of the formula I ##STR1## (X=NOCH3, CHOCH3, CHCH3 ; Y=O, NZ, where Z=H, alkyl; R1 =H, alkyl; R2 =cyano, nitro, trifluoromethyl, halogen, alkyl, alkoxy; m=0, 1, 2, it being possi...
03/28/2000
6013836Insecticidal N'-substituted-N,N'-disubstitutedhydrazines
This invention relates to N'-substituted-N,N'-disubstitutedhydrazines of formula I ##STR1## wherein X and X' are independently O, S, or NR; A' and B' are independently substituted or unsubstituted aryl or aromatic heterocycle; wherein F is alkyl...
01/11/2000
5942644Precursors for the production of chiral vicinal aminoalcohols
The disclosure describes new compositions of matter useful for the preparation of optically-active vicinal aminoalcohols. The compositions are chiral ଲ-hydroxycarboxamides, ଲ-hydroxyhydraxides, and ଲ-hydroxyhydroxamic acids....
08/24/1999
5767314Selective acylation of monoalkylhydrazines
A process for selectively monoacylating monoalkylhydrazines by reacting such with trichloromethyl aryl ketones....
06/16/1998
5747535Selective thrombin inhibitors
The present invention relates to a novel selective thrombin inhibitor having the following formula (I), which is also effective by oral administration: ##STR1## in which R1 represents acetyl substituted with aryl or aryloxy, or repres...
05/05/1998
5700831Pesticidal hydrazide derivatives
A compound of the formula ##STR1## wherein R is a) phenyl; phenyl(C1 -C4 alkoxy); phenoxy; or benzyl; the phenyl ring of each substituent being optionally substituted with one or more of halogen, nitro, C1 -C8
12/23/1997
5693860Amidrazones and their use as insecticidal and acaricidal agents
There are provided substituted acid amide, arylhydrazone compounds (amaidrazones) of formula I ##STR1## the use thereof for the control of insect and acarid pests and methods and compositions for the protection of crops from the damage and loss cause...
12/02/1997
5675037Selective acylation of hydrazines
This application relates to a process for selectively monoacylating hydrazines by reacting unsubstituted or monoalkylhydrazines with trichloromethyl aryl ketones....
10/07/1997
5672723Process for preparation of 1-acyl-2-substituted hydrazines
The present invention can provide a process for the preparation of an 1-acyl-2-substituted hydrazine compound from a mixture containing the 1-acyl-2-substituted hydrazine and an 1-acyl-1-substituted hydrazine by selective hydrolysis or alcoholysis of the ...
09/30/1997
5543571Preparation of optically active hydrazines and amines
A process for the asymmetric hydrogenation of N-acylhydrazones to optically active N-acylhydrazines in the presence of a chiral phospholane catalyst complex, a process for the reductive N--N bond cleavage of N-acylhydrazine to amines with samarium diiodid...
08/06/1996
5541321Process for the preparation of a substituted diaminoalcohol
A process is disclosed for the preparation of a substituted diaminoalcohol of the formula: ##STR1##...
07/30/1996
5541320Process for the preparation of a substituted diaminoalcohol
A process is disclosed for the preparation of a substituted diaminoalcohol of the formula: ##STR1##...
07/30/1996
5523325Amidrazones and their use as pesticides
This invention relates to amidrazones, insecticidal amidrazone compositions, and methods of using such compositions....
06/04/1996
5480871Peptoid ଱-1 adrenergic receptor ligands
Compounds of the formula: ##STR1## are useful for treating conditions modulated by 댑 -adrenergic receptors....
01/02/1996
5451607Hydrazone derivatives, process for producing same, insecticides and/or acaricides containing same as active ingredient and intermediate compounds thereof
There are disclosed hydrazone derivatives of the general formula [I]: ##STR1## wherein R1 is halogen, etc.; R2 is hydrogen or C1 -C6 alkyl, etc.; R3 is hydrogen or C1 -C6 alkyl, ...
09/19/1995
5447916Peptoid alpha-1 adrenergic receptor ligands
Compounds of the formula: ##STR1## are useful for treating conditions modulated by 댑 -adrenergic receptors....
09/05/1995
5445888Hydrazine compound, process for the preparation of the same, and nonlinear optical organic material
A novel hydrazine compound represented by the formula (I) is disclosed. ##STR1## Also disclosed are a process for preparing the novel hydrazine compound comprising reacting a specific hydrazine compound and a specific acid halide, a nonlinear optical...
08/29/1995
5426223Preparation of optically active hydrazines and amines
A process for the asymmetric hydrogenation of N-acylhydrazones to optically active N-acylhydrazines in the presence of a chiral phospholane catalyst complex, a process for the reductive N--N bond cleavage of N-acylhydrazine to amines with samarium diiodid...
06/20/1995
5399758Diacylhydrazine photo-reactive compounds
Disclosed are a novel azide compound represented, for example, by the formula, ##STR1## wherein Rf represents a fluoroalkyl or fluoroalkylpolyether group, ##STR2## wherein R represents a divalent organic group having an ester bond, an...
03/21/1995
5358965Hydrazone derivatives, processes for production thereof, and uses thereof
The present invention relates to a hydrazone derivative represented by the general formula (I) shown below: ##STR1## wherein the substituents are as defined in the specification, processes for preparing the derivative, and uses of the derivative as a...
10/25/1994
5302744Phenolic-hydrazide compounds and polyolefin compositions stabilized therewith
Disclosed are a class of phenolic-hydrazide compounds of diverse structure which are useful as stabilizers for polyolefins. The phenolic-hydrazide compounds inhibit oxidative degradation of polyolefins which is attributable to heat and/or ultraviolet ligh...
04/12/1994
5300676Herbicidal fluorine-substituted alpha-(5-aryloxynaphthalen-1-yl-oxy)-propionic acid derivatives
Fluorine-substituted ଱-(5-aryloxy-naphthalen-1-yl-oxy)-propionic derivatives of the formula ##STR1## wherein R1, R2, R3, R4 and R5, as defined herein, are useful as herbicides. Processes an...
04/05/1994
5294643Cinnamamide derivative
Novel cinnamamide derivatives and the salts thereof are provided. An antihyperlipidemic composition is also provided. The composition comprises an active ingredient which is at least one selected from the group consisting of the above-mentioned cinnamamid...
03/15/1994
5250731Preparation of optically active hydrazines and amines
A process for the asymmetric hydrogenation of N-acylhydrazones to optically active N-acylhydrazines in the presence of a chiral phospholane catalyst complex, a process for the reductive N--N bond cleavage of N-acylhydrazine to amines with samarium diiodid...
10/05/1993
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