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Class 558/417 - The carbonyl is bonded directly to two non-carbon atoms, or to a non-carbon atom and an additional carbonyl (e.g., carbamates, oxamides, etc.)


Subclass of Class 558 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein two noncarbon atoms, or a noncarbon atom
No. of patents: 173
Last issue date: 09/14/2010


1          
NumberTitleIssue Date
7795465Method for producing semicarbazones
The invention relates to a process for preparing semicarbazone compounds of the formula I, where R1 and R2 are each independently hydrogen, halogen, CN, C1-C4-alkyl, C1-C4-alkoxy, C1-C...
09/14/2010
7371885Cis-trans isomerisation of semicarbazone compounds
The present invention relates to the isomerization of the Z-isomer I-Z of semicarbazone compounds of the general formula (I) into its E-isomer I-E, where the variables in formula (I) have meanings given in claim 1 ...
05/13/2008
7176201Modulation of anxiety through blockade of anandamide hydrolysis
Fatty acid amide hydrolase inhibitors of the Formula: are provided wherein X is NH, CH2, O, or S; Q is O or S; Z is O or N; R is an aromatic moiety selected from the group consisting of substituted or ...
02/13/2007
7087642Inhibitors of IMPDH enzyme
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 suited for inhibiting IMPDH e...
08/08/2006
7026500Halogenated selective androgen receptor modulators and methods of use thereof
This invention provides a class of androgen receptor targeting agents (ARTA). The agents define a new subclass of compounds, which are selective androgen receptor modulators (SARM). Several of the SARM compounds have been found to have an unexpected androgenic and a...
04/11/2006
6998500Selective androgen receptor modulators and methods of use thereof
This invention provides a class of androgen receptor targeting agents (ARTA). The agents define a new subclass of compounds, which are selective androgen receptor modulators (SARM). Several of the SARM compounds have been found to have an unexpected androgenic and a...
02/14/2006
6905762Non-aqueous electrolyte solutions comprising additives and non-aqueous electrolyte cells comprising the same
A non-aqueous electrolyte to be used in a Li-ion battery includes a lithium salt, a cyclic carbonate, a linear carbonate and an isocyanate-based additive, with the following general formula R1—N═C═O wherein R1 represen...
06/14/2005
6528543Urea derivatives
Glucokinase activating compounds of the formula ##STR1## wherein R1 and R2 are independently hydrogen, halo, amino, nitro, cyano, sulfonamido, lower alkyl, perfluoro-lower alkyl, lower alkyl thio, perfluoro-lower alkyl thio, lower al...
03/04/2003
6515023Thrombin receptor antagonists
A thrombin receptor antagonist having the formula ##STR1## useful for inhibiting the aggregation of blood platelets. The compounds can be used in a method of acting upon a thrombin receptor which comprises administering a therapeutically effective but non...
02/04/2003
6498178Inhibitors of IMPDH enzyme
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 suited for inhibit...
12/24/2002
6479543Synergistic insecticidal compositions
The present invention provides a synergistic insecticidal composition comprising as essential active ingredients a neuronal sodium channel antagonist in combination with one or more compounds selected from the group consisting of pyrethroids, pyrethroid-t...
11/12/2002
6294573Reverse hydroxamate inhibitors of matrix metalloproteinases
Compounds having the formula ##STR1## are matrix metalloproteinase inhibitors. Also disclosed are matrix metalloproteinase-inhibiting compositions and methods of inhibiting matrix metalloproteinase in a mammal....
09/25/2001
6262113IL-8 receptor antagonists
The present invention relates to novel compounds and a novel use of phenyl ureas in the treatment of disease states mediated by the chemokine Interleukin-8 (IL-8)....
07/17/2001
6252083Carbamates and crop protection agents containing them
Carbamates of the formula I ##STR1## where the substituents have the following meanings: Z is methoxy, NH2, NHCH3, N(CH3)2, CH3, C2 H5, CF3 or CCl3, X and Y are ...
06/26/2001
6225345Azahexane derivatives as substrate isosters of retroviral asparate proteases
The invention relates to compounds of formula (I): ##STR1## wherein R1 and R10 are each independently of the other lower alkoxycarbonyl; either R2, R3 and R4 are each independently of the other C...
05/01/2001
6194454Cyano containing oxamic acids and derivatives as thyroid receptor ligands
The present invention provides novel compounds of the Formula ##STR1## and prodrugs thereof, geometric and optical isomers thereof, and pharmaceutically acceptable salts of such compounds, prodrugs and isomers, wherein R1 -R8 and X a...
02/27/2001
6080860Methods of making ureas and guanidines including, terazosin, prazosin, doxazosin, tiodazosin, trimazosin, quinazosin and bunazosin (exemplary of 2-substituted quinazoline compounds), and meobentine, and bethanidine and intermediates therefor
Novel methods for the synthesis of substituted ureas and guanidines including Terazosin, Prazosin, Doxazosin, Tiodazosin, Trimazosin, Quinasin and Bunazosin (exemplary of 2-amino substituted Quinazolines), Meobentine and Bethanidine and novel intermediate...
06/27/2000
6075148Carbamates and crop protection agents containing them
Carbamates of the formula I where the substituents have the following meanings: Z is methoxy, NH2, NHCH3, N(CH3)2, CH3, C2 H5, CF3 or CCl3, X and Y are identical...
06/13/2000
6057269Benzylhydroxylamines and intermediates used to prepare them
Benzylhydroxylamines I ##STR1## (X=--N(R7)--O--; Y=O, S; R1 =halogen, CN, NO2, CF3 ; R2 =H, halogen; R3 =H, NH2, CH3 ; R4 =H, halogen, C1 -C...
05/02/2000
5981595Sulfonyl urea and carbamate ACAT inhibitors
A pharmaceutically useful compound which lowers blood cholesterol levels having the formula ##STR1## wherein X is oxygen or --NH--; Ar is phenyl, substituted phenyl, naphthyl or substituted naphthyl; R1 is hydrogen, lower alkyl or benzyl; ...
11/09/1999
5922767Substituted benzylurea derivatives and medicine containing the same
Disclosed herein are substituted benzylurea derivatives represented by the following general formula (1): ##STR1## wherein R1 and R2 are independently H, a halogen atom, or an alkyl or alkoxyl group, R3 is a phenyl or...
07/13/1999
5919824Aminophenol derivatives
Aminophenol derivatives represented by the following formula (1): ##STR1## wherein X is O or S; A is alkylene, R1 is phenyl, etc., R2 and R3 are H or alkyl; R4 is substituted carbamoylalkyl, etc.; R5
07/06/1999
58832823-(3-aryloxyphenyl)-1-(substituted methyl-s-triazine-2,4,6-oxo or thiotrione herbicidal agents
There is provided a 3-(3-aryloxyphenyl)-1-(substituted methyl)-s-triazine-2,4,6-oxo or thiotrione compound having the structural formula I ##STR1## Further provided are a composition and a method comprising that compound for the control of undes...
03/16/1999
5856559Process for preparing substituted aryluracils
The invention relates to a novel process for preparing substituted aryluracils by reacting aminoalkenoic esters with arylurethanes and then with sulfonamides, and additionally to novel 4-(alkoxycarbonylamino)-2,5-difluorobenzonitriles....
01/05/1999
5854283Halogen substituted carbamate compounds from 2-phenyl-1,2-ethanediol
The optically pure forms of monoocarbamates of halogenated 2-phenyl-1,2-ethanediol and dicarbamates of 2-phenly-1,2-ethaniediol have been found to be effective in the treatment of disorders of the central nervous system, especially as anti-convulsive or a...
12/29/1998
5723646Substituted amino acid amide derivatives their preparation and use as fungicides
There are described new amino acid amide derivatives, some of which are known, of the formula (I) ##STR1## in which R1 to R8 have the meaning given in the description, and a process for their preparation. The amino acid amide de...
03/03/1998
5543573Hydrazinecarboxyamide derivatives, a process for production thereof and uses thereof
The present invention relates to a hydrazinecarboxamide derivative of the general formula (I) shown below: ##STR1## wherein the substituents are as defined in the specification, which has a wide insecticidal spectrum at a low dosage, a process for pr...
08/06/1996
5446067Oxime ethers and fungicides containing them
Oxime ethers of the formula ##STR1## wherein m, G, R, R1, X, Y, and Z are as defined herein and fungicides containing these compounds....
08/29/1995
5412079Liquid crystal monomer compound and polymer obtained therefrom
Disclosed is a liquid crystal monomer compound represented by formula (1): ##STR1## wherein n is an integer of from 2 to 18, X is direct bond, --(C.dbd.O)--O--, --(C.dbd.O)--NH-- or --N.dbd.N--, R1 is hydrogen or a lower alkyl group, and R...
05/02/1995
5380941Preparation of aromatic ureas which contain a thioether or sulfonyl group
A process for preparing ureas of the formula ##STR1## where the ring A can be substituted and benzo-fused and n is 0 or 2, R4 and R5 are hydrogen, C1 -C4 -alkyl or phenyl, L is unsubstituted or substituted C2
01/10/1995
53627472-nitroaryl and 2-cyanoaryl compounds as regulators of nitric oxide synthase
2-Nitroaryl or 2-cyanoaryl compounds of the formula ##STR1## pharmaceutical compositions thereof, intermediates useful in the preparation of these compounds, and methods for treating disorders of vascular smooth muscles or diseases of the cartilage, ...
11/08/1994
5326899Process for preparation of iodopropargyl carbamates
A Process for producing N-alkyl iodopropargyl carbamate comprising: A. reacting a dialkyl(C1 -C3) carbonate with propargyl alcohol in the presence of a first catalyst under conditions to produce dipropargyl carbonate; B. reacting said dip...
07/05/1994
5319139Naphthalene derivatives
Compounds of the formula: ##STR1## where R1 is a hydrogen atom or a lower alkyl group; R2 is a lower alkoxy group; R3 is a group ##STR2## Z is represented by the formula: ##STR3## where R2 and R
06/07/1994
52889012-aryl-5-(trifluoromethyl)-2-pyrroline compounds useful in the manufacture of insecticidal, nematocidal and acaricidal arylpyrroles
There are provided important pyrroline and glycine intermediates, methods for the preparation of said intermediates and the use thereof in the manufacture of arylpyrrole insecticidal agents....
02/22/1994
5220022Compositions useful as dot promoting agents
Disclosed are novel compounds of the formula ##STR1## wherein: R is ##STR2## where Ph is phenyl, or ##STR3## X is --NR5 R6 or --OR7 ; R1 and R2 are independently hydrogen, methyl, ...
06/15/1993
51589532-substituted methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-ones (thiones), the preparation and use thereof
The present invention provides a novel series of 2-substituted methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-ones (-thiones) compounds. These compounds are found useful as an active ingredient for the prophylaxis and treatment of hypertension....
10/27/1992
5153223Biurets, aminocarbonyl carbamates, and aminocarbonyl thiocarbamates useful as ACAT inhibitors
Novel compounds useful as ACAT inhibitors having the formula ##STR1## wherein Q is R5 O; R5 S-- or NR3 R4 ; wherein R is hydrogen or alkyl C1 -C20 or --CH2 Ph; wherein R1
10/06/1992
5130454Polytetrahydrofuran derivatives having terminal aromatic groups
Polytetrahydrofuran derivatives of the general formula ##STR1## where n is from 2 to 70, X is the bridge member --NH-- or --O-- and R1 and R4 are each hydrogen or various radicals....
07/14/1992
5078783Substituted alkyl carbamates and their use as herbicides
Substituted 1-alkyl carbamates of the formula ##STR1## in which: R is a member selected from the group consisting of halogen, trifluoromethyl, cyano, NO2 and C1 -C3 haloalkyloxy; R1 is selected from the group co...
01/07/1992
5061796Azamethine compounds
This invention provides azamethine compounds represented by the formula (I): ##STR1## (wherein X represents ##STR2## Y represents C.dbd.O, C.dbd.C(CN)2 or SO2 ; R1 to R4 represent independently a ...
10/29/1991
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