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Class 514/210.15 - Chalcogen bonded directly to the ring nitrogen of the four-membered ring


Subclass of Class 514 - Drug, bio-affecting and body treating compositions
Definition: Subject matter wherein a chalcogen (i.e. oxygen, sulfur,
No. of patents: 45
Last issue date: 07/05/2011


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NumberTitleIssue Date
7973029Inhaled aztreonam lysine for the treatment of deficits in health-related quality-of-life in lung diseases
Provided is a method of treating the health-related quality-of-life (HRQOL) symptoms of a lung disease, comprising the administration of an inhalable aerosol of aztreonam lysine. The method is suitable for the short term and sustainable long term treatment of HRQOL ...
07/05/2011
7846920Heterosubstituted N-thiolated beta-lactam compounds and methods of use
The invention relates to heterosubstituted N-thiolated beta-lactams, compositions comprising these compounds, methods for their production, and methods of use as antibiotics to inhibit the growth of bacteria. In one embodiment, the compounds have the structure shown...
12/07/2010
7635693Methods for preventing and treating cancer using -thiolated β-lactam compounds and analogs thereof
The subject invention concerns N-thiolated β-lactam compounds of formula A, wherein R1 is a hydrocarbon group having 1-8 carbon atoms; R3 is an organothio group; and R4 is alkyl, alkenyl, a...
12/22/2009
7439253Heterocyclic compounds, their preparation and their use as medicaments, in particular as antibacterials and beta-lactamase inhibitors
The invention relates to novel heterocyclic compounds of general formula (I), and their salts with a base or an acid: The invention also relates to a method for preparing these compounds, and to their use as medicaments, in p...
10/21/2008
7358093Aztreonam L-lysine and methods for the preparation and analysis thereof
The present invention relates to the L-lysine salt of aztreonam and methods for making the L-lysine salt of aztreonam. ...
04/15/2008
7282221Antiviral product, use and formulation thereof
An antiviral product is comprised of at least three dosages forms, each of which has a different release profile, with the Cmax for the antiviral product being reached in less than about twelve hours. In one embodiment, there is an immediate release dosag...
10/16/2007
7262293Aztreonam L-lysine and methods for the preparation thereof
The present invention relates to the L-lysine salt of aztreonam and methods for making the L-lysine salt of aztreonam. ...
08/28/2007
7214364Inhalable aztreonam lysinate formulation for treatment and prevention of pulmonary bacterial infections
A method and a composition for treatment of pulmonary bacterial infections caused by gram-negative bacteria suitable for treatment of infection caused by Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Pseudomonas aeruginosa, Haemophilus influenzae, ...
05/08/2007
6946458N-thiolated beta-lactams: novel antibacterial agents for methicillin-resistant Staphylococcus aureus
The invention relates generally to novel N-thiolated β-lactams. More specially, the invention relates to the use of these novel antibacterial agents in the treatment or inhibition of methicillin-resistant Staphylococcus aureaus. ...
09/20/2005
69168033-(Heteroaryl acetamido)-2-oxo-azetidine-1-sulfonic acids derivatives as antibacterial agents
The present invention relates to novel Syn isomers of racemates and optical isomers of 3-(heteroaryl acetamido)-2-oxo-azetidine-1-sulfonic acids of the following formula: and their use in treating infections caused by ...
07/12/2005
68219634-Bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors
Phenylamino benzhydroxamic acid derivatives of formula (I) where R1, R2, R3, R4, R5, and R6 are hydrogen or substituent groups such as alkyl, and where R7 is hydrogen or an organic radical,...
11/23/2004
6476015N-thiolated ଲ-lactam antibiotics
Substituted monocyclic ଲ-lactam compounds that are N-1-thiolated monolactams, and which exhibit wide-ranging antibacterial activities, having a single 4-membered azetidinone ring in which: the N-1 nitrogen atom of the azetidinone ring is bonded to s...
11/05/2002
6335324Beta lactam compounds and their use as inhibitors of tryptase
Compounds of the formulas: ##STR1## are disclosed. These compounds inhibit tryptase as well as other enzyme systems or are selective tryptase inhibitors and are useful as antiinflammatory agents particularly in the treatment of chronic asthma....
01/01/2002
60340774-substituted-3-(2-amino-2-cycloalkyl methyl)-acetamido azetidin-2-one derivatives as cysteine proteinase regulators
In accordance with the present invention, there are provided 4-substituted-3-(2-amino-2-cycloalkyl methyl)-acetamido azetidin-2-one derivatives of the formula: ##STR1## wherein n is 1, 2 or 3; in which R1, R2 and R3 a...
03/07/2000
5994340Azetidinone derivatives as ଲ-lactamase inhibitors
New 2-oxo-1-azetidine sulfonic acid derivatives with an aminoalkyl substituted "anti" (E-isomer) oxyimino group in the acylamino substituent at the 3 position of the monobactam ring. These compounds are potent inhibitors of bacterial ଲ-lactamases. T...
11/30/1999
59168874-substituted-3-(2-amino-2-cycloalkyl methyl)-acetamido azetidin-2-one derivatives as cysteine proteinase regulators
In accordance with the present invention, there are provided 4-substituted-3-(2-amino-2-cycloalkyl methyl)-acetamido azetidin-2-one derivatives of the formula: ##STR1## wherein n is 1, 2 or 3; in which R1, R2 and R3 a...
06/29/1999
58889982-oxo-1-azetidine sulfonic acid derivatives as potent ଲ-lactamase inhibitors
A compound of formula (I) ##STR1## wherein R1 is selected from the group consisting of 2-thienyl, 2-furyl, 2-pyrrolyl, 1-methyl-2-pyrrolyl, 2-amino-1-thiazolyl and 5-isothiazolyl; R2 is selected from the group consisting of: ...
03/30/1999
5318963Heterocyclic hydrazide derivatives of monocyclic ଲ-lactam antibiotics
Antibacterial activity has been found in compounds of the formula. Compounds having the formula ##STR1## and pharmaceutically acceptable salts thereof, wherein: A is a bond or alkylene; Q completes a 5- or 6-membered saturated or unsaturated (including ...
06/07/1994
52505254-oxo-azetidine-2-sulfonic acids and their salts, processes for the preparation thereof and their use
The invention relates to novel 4-oxo-azetidine-2-sulfonic acids and their salts or the formula I ##STR1## wherein: R1 =hydrogen, halogen, phenylacetamido; R2 =hydrogen, halogen, phenylacetamido, phenoxyacetamido, phthalimido, 5-...
10/05/1993
5143913[3S(Z)]-3-[[(2-amino-4- thiazolyl)[[2-(hydroxyamino)-2-oxoethoxy]imino]acetyl]amino]-2,2-dimethyl -4-oxo-1-azetidinyl sulfate
The compound [3S(Z)]-3-[[(2-amino-4-thiazolyl)[[2-(hydroxyamino)-2-oxoethoxy]imino]acet yl]amino]-2,2-dimethyl-4-oxo-1-azetidinyl sulfate has gram-positive and gram-negative activity and good oral absorption....
09/01/1992
5120729Beta-lactams as antihypercholesterolemics
This application relates to compounds of formula (I), which are useful as antihypercholesterolemic agents. ##STR1##...
06/09/1992
5110812Azetidin-2-one derivatives as serine protease inhibitors
The present invention relates to new 3-guanidinoalkyl-2-azetidinones of the formula ##STR1## wherein: U and W can be the same or different and are selected from the group consisting of hydrogen and an amino protecting group; n is 1 to 3; X is a membe...
05/05/1992
50575123-amino-2-oxo-azetidine-1-sulfonic acids
Novel syn isomers of reacemates and optical isomers of 3-amino-2-oxo-azetidine-1-sulfonic acids of the formula ##STR1## wherein R is difluoromethyl, R1 is --(CH2)n --X, n is an integer from 1 to 4, X is selected from ...
10/15/1991
5039672Heterocyclic compounds as aldose reductase inhibitors
Certain spirocyclic heterocyclic compounds, and their pharmaceutically-acceptable salts, are inhibitors of the aldose reductase enzyme, and so are useful for the control of diabetic complications. Exemplary compounds include compounds of the formula ...
08/13/1991
4983597Beta-lactams as anticholesterolemic agents
Compounds of formula (I), which are useful as antihypercholesterolemic agents, are disclosed. ##STR1##...
01/08/1991
4946838Crystalline anhydrous aztreonam
The crystalline anhydrous form of [3S-[3଱(Z), 4ଲ]]-3-[[(2-amino-4-thiazolyl) [(1-carboxy-1-methylethoxy)imino]acetyl]amino]-4-methyl-2-oxo-1-azetidines ulfonic acid is prepared....
08/07/1990
4900728Novel 3-amino-2-oxo-azetidine-1-sulfonic acids
Novel syn isomers of racemates and optical isomers of 3-amino-2-oxo-azetidine-1-sulfonic acids of the formula ##STR1## wherein R is selected from the group consisting of hydrogen linear or branched optionally substituted alkyl of 1 to 12 carbon atoms...
02/13/1990
48227881-sulfo-2-oxozetidine derivatives and their product ion
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 wherein R is an organic residue attached to the az...
04/18/1989
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
47941081-carboxymethoxy acetidinones and their production
A 2-azetidinone derivative having a group of the formula ##STR1## wherein R1 and R2 are the same or different and each represents a hydrogen atom, alkyl, aryl or arylalkyl which may have a substituent at the 1-position and an am...
12/27/1988
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
47710452-oxozetidinone derivatives, their production and use
Novel 1-sulfo-2-oxoazetidine derivatives and their production and use. These 1-sulfo-2-oxoazetidine derivatives exhibit excellent antimicrobial activity against gram-positive and gram-negative bacteria, and ଲ-lactamase inhibitory activity, thus being of ...
09/13/1988
4751220Crystalline salts of [3S(Z)]-2[[[1-(2-amino-4-thiazolyl)-2-[[2,2-dimethyl-4-oxo-1-(sulfooxy)- 3-azetidinyl]amino]-2-oxoethylidene]-amino]oxy]acetic acid
In accordance with the present invention an orally active monosulfactam antibiotics having a crystalline structure and thereby improved stability are disclosed. The antibiotics comprise the dierythromycin (M.sym.=erythromycin.H.sup..sym.) salt ...
06/14/1988
4725591ଲ-lactamase inhibitory composition
Compounds having one or two substituents at the 3-position, represented by the general formula ##STR1## wherein R1 is an optionally acylated or protected amino group and X is hydrogen atom or methoxy group, or a pharmaceutically acceptable...
02/16/1988
4680388O-sulfated spiro ଲ-lactam hydroxamic acids
Antibacterial activity is exhibited by compounds having the formula and pharmaceutically acceptable salts thereof....
07/14/1987
4680391Substituted azetidinones as anti-inflammatory and antidegenerative agents
New substituted azetidinones are found to be potent elastase inhibitors and thereby useful anti-inflammatory/antidegenerative agents....
07/14/1987
46650671-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 wherein R is an organic residue attached to the az...
05/12/1987
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
45728014-Carbamoyloxymethyl-1-sulfo-2-oxoazetidine derivatives and their production
Disclosed are compounds of the general formula: ##STR1## wherein R1 is a hydrogen atom or a lower alkyl group and R2 is a hydrogen atom or an ester residue, said derivative having the (3S,4S)-configuration; and pharmaceutically ...
02/25/1986
45512762-Oxoazetidin-1-yloxymethyl sulfonic acid and analogs
Antibiotic activity is exhibited by ଲ-lactams having an ##STR1## substituent in the 1-position and an acylamino substituent in the 3-position....
11/05/1985
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