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Class 560/18 - Ester function attached directly to a ring


Subclass of Class 560 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein the esterified carboxylic acid function
No. of patents: 309
Last issue date: 04/02/2013


1                
NumberTitleIssue Date
8410301Methods for the synthesis of organic sulfides by using sulfides and organic sulfur-indium complexes
The present invention relates to a novel synthesis method for the formation of carbon-sulfur bonds by the reaction of an organic sulfur-indium complex with nucleophile in the presence of a palladium catalyst. The present invention provides a synthesis method to prep...
04/02/2013
7393873Arylsulfonamide derivatives
N-aryl arylsulfonamide derivatives are bradykinin B1 antagonists or inverse agonists useful in the treatment or prevention of symptoms such as pain and inflammation associated with the bradykinin B1 pathway. ...
07/01/2008
7285686Process for the preparation of 1,3-substituted indenes
An improved process for the preparation of 1,3 substituted indenes which are useful intermediates in the synthesis of aryl fused azapolycyclic compounds as agents for the treatment of neurological and psychological disorders. ...
10/23/2007
7271196CETP activity inhibitors
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 cha...
09/18/2007
7250159Compositions comprising at least one ester of at least one hydroxylated aliphatic compound
Compositions comprising at least one ester which comprises at least one aromatic group, which is liquid at room temperature and which is derived from esterification with (i) at least one aromatic acid of (ii) at least one hydroxyl group of at least one hydroxylated ...
07/31/2007
7208510Fungicidal combinations of active substances
The present invention relates to fungicidally active compound combinations of a fluorobenzothiazole derivative of the formula (I) and at least one of the compounds listed in the disclosure. ...
04/24/2007
7205428Thioether derivatives, their method for production and use
The present invention is directed to novel thioether dendritic molecules which respond immediately by emission of light when stimulated with light or electric energy. ...
04/17/2007
7186870Process for the preparation of 1,3-substituted indenes and aryl-fused azapolycyclic compounds
The present invention relates to processes for the preparation of any of the intermediate 1,3-substituted indenes of the formulae (Ia), (Ib) and (Ic) or a mixture thereof: wherein R1, R2, R
03/06/2007
7157458Bifunctional energy-reversible acyl-compositions
Energy-reversible acyl conjugates, intermediates, and related compositions are disclosed. In preferred aspects, examples of such compositions include: ...
01/02/2007
7115593Fungicidal combinations of active substances
The present invention relates to active compound combinations of a fluorobenzo-thiazole of the formula (I) and at least one of the compounds listed herein. The active compound combinations of the present inventio...
10/03/2006
7094919Preparation of substituted aromatic carboxylic acid esters
Methods for preparing substituted aromatic carboxylic acid esters are described. In particular, the invention relates a method for preparing a nitro-substituted aromatic carboxylic acid ester: Additionally the inventio...
08/22/2006
7091372Process for the preparation of 1,3-substituted indenes and aryl-fused azapolycyclic compounds
The present invention relates to processes for the preparation of any of the intermediate 1,3-substituted indenes of the formulae (Ia), (Ib) and (Ic) or a mixture thereof: wherein R1, R2, R
08/15/2006
7078540Substituted aromatic-ring compounds, process for producing the same, and use
A compound of the formula: wherein R1 is an aliphatic hydrocarbon group optionally having substituent(s), an aromatic hydrocarbon group optionally having substituent(s), a heterocyclic group optionally...
07/18/2006
6860905Anionic phthalic acid ester compounds and stain resistant compositions
This invention relates to compounds of formula: wherein A is an unsaturated alkylene moiety; B the residue of a polyol wherein one hydroxyl moiety is esterified with one carboxyl moiety of the phthalic acid moiety; D i...
03/01/2005
6846890Norbornene derivative and norbornene polymer obtained therefrom through ring opening polymerization
A novel norbornene derivative represented by a general formula (1m) shown below is provided. By conducting a ring opening polymerization of this norbornene derivative, or by performing a subsequent hydrogenation following the ring opening polymerization, a ring open...
01/25/2005
6777575Process for the preparation of 2-alkylthio benzoic acid derivatives
A process for preparing a compound of the formula comprising reacting a compound of the formula wherein R3 is nitro or halo, or a salt thereof, with a compound of ...
08/17/2004
6649656Anthranilic acid derivatives
The present invention relates to an anthranilic acid derivative expressed by the following formula (1) or the following formula (2), or its pharmacologically permissible salt or solvate. ##STR1##...
11/18/2003
6638977Plasminogen activator inhibitor antagonists
Compounds and pharmaceutical compositions useful as plasminogen activator inhibitor (PAI) antagonists are provided. In particular, methods of antagonizing PAI with substituted and unsubstituted aryl and heteroaryl ethers and thioethers are provided....
10/28/2003
64982653-amino-2-mercaptobenzoic acid derivatives and processes for their preparation
Compounds of the formula I ##STR1## and disulfides thereof and salts thereof are important intermediate products for the preparation of compounds having a microbicidal and plant-immunizing action, of the formula III ##STR2## In the compounds of the f...
12/24/2002
6495710Synthesis and use of dimethyl 1,5-naphthalenedicarboxlyates and intermediates therefrom
The synthesis of dimethyl-1,5-naphthalenedicarboxylate and polymers and articles formed therefrom is disclosed, as well as applications for dimethyl-1,5-naphthalenedicarboxylate, its corresponding acid 1,5-NDA, and various synthesis intermediates....
12/17/2002
6479550଱-sulfenimino acid derivatives
଱-Sulfenimino acid derivatives of formula I ##STR1## including the optical isomers thereof and mixtures of such isomers, wherein A is cycloalkyl, cycloalkenyl, aryl or heteroaryl, each optionally substituted, B is a direct bond or optionally substituted ...
11/12/2002
6369261Compounds having activity as inhibitors of cytochrome P450RAI
Compounds having Formula 2 wherein the symbols have the meaning defined in the specification are inhibitors of the cytochrome P450RAI (retinoic acid inducible) enzyme, and are used for treating diseases responsive to treatment by retinoids. ##STR1##...
04/09/2002
6337418Preparation of C1-C5 alkyl esters of nitro or thioether substituted aromatic carboxylic acids
Methods for preparing substituted aromatic carboxylic acid esters are described. In particular, the invention relates a method for preparing a nitro-substituted aromatic carboxylic acid ester: ##STR1## Additionally the invention relates to a method for pr...
01/08/2002
6337350Inhibitors of formation of advanced glycation endproducts (AGEs)
Derivatives of aryl and heterocyclic ureido and aryl and heterocyclic carboxamido phenoxy isobutyric acids have been found to inhibit the nonenzymatic glycation of proteins which often results in formation of advanced glycation endproducts and crosslinks....
01/08/2002
6262293ω-Cycloalkly-prostaglandin e2 derivatives
ω-Cycloalkyl-prostaglandin E2 derivatives of formula (I) ##STR1## (wherein all symbols are as defined in the description); and non-toxic salts thereof, prodrugs thereof and cyclodextrin clathrates thereof. Compounds of formula (I) strongly bind on ...
07/17/2001
6187812Phenylacetic acid derivatives, preparation thereof and intermediates therefor, and compositions containing them
Phenylacetic acid derivatives of the formula I ##STR1## where the substituents and the index have the following meanings: X is oxygen or sulfur; R is hydrogen or alkyl; R1 is hydrogen or alkyl; R2 is cyano, nitro, trifluoromethyl, halogen, alk...
02/13/2001
6140528Intermediates to herbicidal isoxazole and 2-cyano-1,3-dione compounds
The invention relates to intermediates to herbicidal compounds of formulae (Ia), (Ib) or (Ic): ##STR1##...
10/31/2000
6072072Compounds for preparing modified hemoglobin
The present invention provides a chemically modified form of hemoglobin that is stabilized and can efficiently bind and release oxygen. In addition the chemically modified hemoglobin may be polymerized to increase its molecular weight and increase its sta...
06/06/2000
6054457Benzamide derivatives and their use as vasopressin antagonists
This invention relates to new benzamide derivatives having a vasopressin antagonistic activity, etc, and represented by general formula (I): ##STR1## wherein R1 is aryl optionally substituted with lower alkoxy, etc., R2 is lower...
04/25/2000
6013606Substituted cinnamic oxime and hydroxamide derivatives
Substituted cinnamic oxime derivatives I and cinnamic hydroxamide derivatives II ##STR1## (R1= halogen, NO2, CN, CF3 ; R2 =H, halogen; R3= H, halogen, C1 -C6 -alkyl, C1...
01/11/2000
5981581Phenylacetic acid derivatives, preparation thereof and intermediates therefor, and compositions containing them
Phenylacetic acid derivatives of the formula I ##STR1##...
11/09/1999
5965524Analogs of viscosin and uses thereof
This invention is directed to the analogs of viscosin, pharmaceutical compositions thereof and to methods of using viscosin and analogs thereof as biosurfactants and as antibacterial, antiviral and antitrypanosomal therapeutic compounds. In particular, co...
10/12/1999
5962651Modified hemoglobin and its use as a component of an artificial blood substitute
The present invention provides a chemically modified form of hemoglobin that is stabilized and can efficiently bind and release oxygen. In addition the chemically modified hemoglobin may be polymerized to increase its molecular weight and increase its sta...
10/05/1999
5952386Dihalopropene compounds, insecticides containing them as active ingredients, and intermediates for their production
The present invention provides dihalopropene compounds of the general formula: ##STR1## wherein R1 is C1 -C10 alkyl or the like; L is C(.dbd.O)NH or the like; R2, R3 and R4 are indepen...
09/14/1999
5945548Process for the synthesis of ଱-substituted acrylic acids and their application
Process for the synthesis of ଱-substituted acrylic acids of general formula (I) and their application to the synthesis of N-(mercaptoacyl)aminoacid derivatives of formula (II). ##STR1##...
08/31/1999
5877297Boronic compound complexing reagents and highly stable complexes
Boron compound completing reagents, intermediate reagents of those reagents and methods of synthesizing these reagents. These reagents, including those shown as General Formula CII may be used, after further reactions described herein, to complex with bor...
03/02/1999
5874608Process for the preparation of esters of aromatic carboxylic acid
The present invention relates to a process for the preparation of compounds of the formula (1) R1 R2 R3 R4 R5 ArCOOR (1) in which R1, R2, R3, R4 and R
02/23/1999
5869623Boronic compound complexing reagents and complexes
Boron compound complexing reagents, intermediate reagents of those reagents, and methods of synthesizing these reagents are disclosed. These reagents, including those shown as General Formula II may be used, after further reactions described herein, to co...
02/09/1999
5847192Boronic compound complexing reagents and complexes
Boron compound complexing reagents and methods of synthesizing these reagents are disclosed. These reagents, including those shown as General Formula I and General Formula II may be used, after further reactions described herein, to complex with boronic c...
12/08/1998
5831102Chemiluminescent 3-(substituted adamant-2'-ylidene) 1,2-dioxetanes
Enzymatically cleavable chemiluminescent 1,2-dioxetane compounds capable of producing light energy when decomposed, substantially stable at room temperature before a bond by which an enzymatically cleavable labile substituent thereof is intentionally clea...
11/03/1998
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