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Class 987/368 - Four-membered ring (9/65A4; 9/65A4E; 9/65A4V)


Subclass of Class 987 - Organic compounds containing a bi, sb, as, or p atom or containing a metal atom of the 6th to 8th group of the periodic system
Definition: Subject matter wherein the compound contains a four-membered
No. of patents: 163
Last issue date: 09/18/1990


1          
NumberTitleIssue Date
49579127 acylamidocarbacephem antibacterial agents
Novel antibiotics of the formula: ##STR1## and its salts, esters and amides wherein R is acyl; B is H, OMe, Me or SR wherein R is lower alkyl or aryl; A1 is hydrogen, hydroxy, or an organic group; and, X is a divalent radical selected from --O--, --...
09/18/1990
49526906-substituted thia-aza compounds
The invention relates to azetidin-2-ones of the formula ##STR1## wherein Ra represents hydroxy-lower alkyl, R1 represents hydrogen, an organic radical bonded by a carbon atom to the ring carbon atom or an etherified mercapto gro...
08/28/1990
4912224Carboxyalkenamidocephalosporins
An antibacterial 7beta-(carboxyalkenoyl)amino-3-cephem-4-carboxylic acid represented by the following formula: ##STR1## (wherein R is aryl or a heterocyclic group; R1 is hydrogen or halogen; R2 is a single bond, alkylene, or thiaalky...
03/27/1990
4853468Process for the preparation of cephem derivatives
This invention provides azetidinone derivatives represented by the formula ##STR1## and processes for preparing the same. The azetidinone derivatives are used as the intermediates for producing cephalosporin compounds useful as antibiotic agents....
08/01/1989
48227901-Sulfo-2-oxoazetidine derivatives and their production
Disclosed are compounds of the general formula: ##STR1## wherein R1 is amino, an acylated amino or a protected amino group, X is hydrogen or methoxy, and R' is hydrogen, R or R4 where R is an organic residue attached to the azet...
04/18/1989
4820815Azetidinone N-phosphonomethyl esters
The invention provides azetidinones of the formula ##STR1## where R4 is hydrogen, amino or protected amino; R0 is H when R4 is amino or protected amino, or C1 -C4 alkyl when R4 is H; R...
04/11/1989
4798828Heterocyclic-methylene-penems
Compounds of the general formula I: ##STR1## and their pharmaceutically acceptable salts and in vivo hydrolyzable esters, in which one of R1 and R2 denotes hydrogen, the other of R1 and R2 denotes an unsubstitut...
01/17/1989
47941096-hydroxy-lower alkylpenem compounds, pharmaceutical preparations that contain these compounds, and the use of the latter
2-Heterocyclyl-lower alkyl-6-hydroxy-lower alkyl-2-penem compounds of the formula ##STR1## in which R1 represents lower alkyl substituted by hydroxy or protected hydroxy, R2 represents carboxy or functionally modified carbo...
12/27/1988
4784734Azetidinone derivatives and process for the preparation of the same
This invention provides azetidinone derivatives represented by the formula ##STR1## and processes for preparing the same. The azetidinone derivatives are used as the intermediates for producing cephalosporin compounds useful as antibiotic agents....
11/15/1988
47756702-oxo-1-azetidinesulfonic acid salts
Antibacterial activity is exhibited by ଲ-lactams having a sulfonic acid salt substituent in the 1-position and an amino or acylamino substituent in the 3-position....
10/04/1988
47756691-carba-2-penem-3-carboxylic acid
Disclosed are 1-carba-2-penem-3-carboxylic acids of the following structure: ##STR1## wherein R1, R2 and R3 are, inter alia, independently selected from the group consisting of hydrogen, alkyl, aryl, and aralkyl. ...
10/04/1988
4761408Crystalline aminomethyl compound
The invention relates to (5R,6S)-2-aminomethyl-6-[(1R)-1-hydroxyethyl]-2-penem-3-carboxylic acid in crystalline form and a process for the manufacture thereof. The substance is suitable for treating infectious diseases....
08/02/1988
4748170Carboxyalkenamidocephalosporins
An antibacterial 7beta-(carboxyalkenoyl)amino-3-cephem-4-carboxylic acid represented by the following formula: ##STR1## (wherein R is aryl or a heterocyclic group; R1 is hydrogen or halogen; R2 is a single bond, alkylene, or thi...
05/31/1988
4743598Antibacterial 2-(azacycloalkyl) penems
Disclosed are 6-(1'hydroxyethyl)-2-(azacycloalkyl)penem-3-carboxylic acids and salts or metabolizable esters thereof having an absolute stereochemistry of 5R,6S,8R. The compounds are useful and potent antibacterial agents and can be formulated into a vari...
05/10/1988
4742052Antibacterial ଲ-lactam compounds
Novel ଲ-lactam compounds classified into penem compounds, a process for preparing the same and use of such ଲ-lactam compounds are disclosed. These ଲ-lactam compounds exhibit excellent antimicrobial activities useful as pharmaceuticals or...
05/03/1988
4740507Carbapenem compounds and use
Compounds of formula (I): ##STR1## (wherein R1 is carboxy, --CONR4 R5, cyano or hydroxymethyl, and R2 and R3 are hydrogen, alkyl or substituted alkyl, R4 and R5 being hydrog...
04/26/1988
4729993Carbapenems and 1-methylcarbapenems having an externally alkylated mono- or bicyclic 2-quaternary heteroarylalkyl substituent
Carbapenems having the formula: ##STR1## wherein ##STR2## is mono- or bicyclic quaternary heteroaryl, their preparation and antibiotic use are disclosed....
03/08/1988
47230021-(substituted phosphorous)-azetidinone antibacterials
Antibacterial activity is exhibited by 2-azetidinones having an acylamino substituent in the 3-position and having an activating group in the 1-position of the formula ##STR1##...
02/02/1988
4716155Phosphorus containing compounds and hypotensive use thereof
Phosphorus containing compounds of the formula ##STR1## wherein X is a substituted or unsubstituted imino or amino acid and A is ##STR2## These compounds possess angiotensin converting enzyme activity and are thus useful as hypertensive agents....
12/29/1987
47043853-formamido azetidinone antibacterial agents, their preparation and use
A monocyclic ଲ-lactam antibiotic having a formamido substituent at the 3S-position, including compounds of the formula (I): ##STR1## and salts thereof wherein R is --SO3 H; --PO(OH)Y wherein Y is C1-6 alkoxy, hydroxy, aryl...
11/03/1987
46924426-substituted penem compounds
The invention relates to 2-penem-3-carboxylic acid compounds of the formula ##STR1## in which Ra represents an organic radical bonded by a carbon atom to the ring carbon atom, a free, etherified or esterified hydroxy or mercapto group or a...
09/08/1987
46894114-thio azetidinone intermediates and process for the preparation of the same
This invention provides azetidinone derivatives represented by the formula ##STR1## and processes for preparing the same. The azetidinone derivatives are used as the intermediates for producing cephalosporin compounds useful as antibiotic agents....
08/25/1987
4686298Intermediates for alpha-acyloxy phosphonate angiotensin converting enzyme inhibitors
Compounds of the formula ##STR1## are useful in the preparation of ଱-acyloxy phosphonate compounds. The final products are useful as anti-hypertensive agents due to their angiotensin converting enzyme inhibition activity....
08/11/1987
46832266-hydroxyalkyl-2-(substituted-thio)penem-3-carboxylic acids
6-substituted-hydrocarbon-2-(substituted-thio)penem-3-carboxylic acids and cogeners having useful antibacterial activity are disclosed. The compounds are prepared in a reaction sequence starting with a 4-acyloxy-2-azetidinone....
07/28/1987
46819373-acylamino-2-oxo-1-azetidinyl esters of phosphonic acids, phosphoric acid and phosphoric acid esters
Antimicrobial activity is exhibited by ଲ-lactams having a ##STR1## substituent in the 1-position and an acylamino substituent in the 3-position, or a pharmaceutically acceptable salt thereof; wherein Y is oxygen or sulfur and R5 is h...
07/21/1987
46787823S-formamido azetidinone antibacterial agents, their preparation and use
A monocyclic ଲ-lactam antibiotic having a formamido substitutent at the 3S-position, including compounds of the formula (I): ##STR1## and salts thereof wherein R is --SO3 H; --PO(OH)Y wherein Y is C1-6 alkoxy, hydroxy, ary...
07/07/1987
4670554((3-Acylamino-2-oxo-1-azetidinyl)oxy)methyl)phosphinic acids
Antibacterial activity is exhibited by ଲ-lactams having a 3-acylamino substituent and in the 1-position a substituent having the formula ##STR1## wherein R5 and R6 are the same or different and each is hydrogen, alkyl, alk...
06/02/1987
4670422଱-acyloxy phosphonate angiotensin converting enzyme inhibitors
Compounds of the formula ##STR1## wherein X is various amino or imino acids and esters are disclosed. These compounds are useful as anti-hypertensive agents due to their angiotensin converting enzyme inhibition activity and depending upon the definit...
06/02/1987
4663450Optically active cephalosporin analogs
Optically active cephalosporin analogs of the formula ##STR1## wherein R2 represents a hydrogen or a group represented by the formula ##STR2## wherein R3 is a straight or branched lower alkyl group having 1 to 6 carbon...
05/05/1987
4659814Salts of amino-beta-lactamic acids and process for the preparation thereof
Amino-beta-lactamic acid salts, having the formula: ##STR1## wherein: (X-Y) may form a system having from 1 to 3 carbon atoms, with or without double bond, (a) closed, in which: X is an atom selected from among carbon, oxygen, nitrogen and sulphur; Y...
04/21/1987
4656165Aminomethyl penem compounds
Compounds of the formula ##STR1## in which R1 is lower alkyl substituted by hydroxy or by protected hydroxy, R2 represents carboxy or functionally modified carboxy, and R3 represents amino, lower alkyl-substituted amino, s...
04/07/1987
4647558Antibacterial agents, their preparation and use
A monocyclic ଲ-lactam antibiotic having a formamido substituent at the 3S-position, including compounds of the formula (I): ##STR1## and salts thereof wherein R is --SO3 H; --PO(OH)Y wherein Y is C1-6 alkoxy, hydroxy, aryl...
03/03/1987
4634697Carboxyalkenamidocephalosporins
An antibacterial 7beta-(carboxyalkenoyl)amino-3-cephem-4-carboxylic acid represented by the following formula: ##STR1## (wherein R is aryl or a heterocyclic group; R1 is hydrogen or halogen; R2 is a single bond, alkylene, or thiaalky...
01/06/1987
4629726Penem carboxylic acids
A 2-substituted or unsubstituted-6-(2-oxo-1, 3-dioxolan-4-yl)-2-penem-3-carboxylic acid derivative represented by the following formula (Ia) and: ##STR1## wherein R is hydrogen, a light metal or a carboxy-protecting group, R1 is an al...
12/16/1986
4625022Process for preparing (s)-3-amino-2-oxo-1-azetidinesulfonic acid salts
The process of this invention provides for the conversion of amino acid amides having the formula ##STR1## to 3-amino-2-oxo-1-azetidinesulfonic acid salts having the formula ##STR2## wherein one of R2 and R3 is hydrogen and...
11/25/1986
46173002(N-heterocyclyl) penems
There are disclosed 2(N-heterocyclyl) penems and their pharmaceutically acceptable salts and esters and their use as anti-bacterials....
10/14/1986
4616007Heterocyclthio compounds, process for their manufacture, pharmaceutical preparations that contain these compounds, and the the use of the latter
2-heterocyclythio-lower alkyl-2-penem compounds of the formula ##STR1## in which R1 represents hydrogen or methyl, R2 represents an optionally protected hydroxy group, R3 represents carboxy or protected carboxy R...
10/07/1986
46007131-, 6- and 2-substituted-1-carba-2-penem-3-carboxylic acids
Disclosed are 1-, 6- and 2-substituted-1-carba-2-penem-3-carboxylic acids of the following structure: ##STR1## wherein R1, R2, R3, R4 and R5 are, inter alia, independently selected from the group...
07/15/1986
4592865Azetidinone intermediates for cephalosporin analogs
Intermediates of the following formula are useful for the synthesis of 1-oxacephalosporins. Their preparation from penicillins and the transformation process to make 1-oxacephalosporins are disclosed. The compounds are of the formula: ##STR1## w...
06/03/1986
45841321-(N-phosphinylcarbamoyl) ଲ-lactam antibacterial agents
A novel family of ଲ-lactam antibacterials, synthetic methods and intermediates useful in the production of such antibacterials, and the use of such compounds as antibacterials are disclosed. The novel compounds have the formula ##STR1## wh...
04/22/1986
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