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sulfazecin

Known as: D-Alaninamide, D-gamma-glutamyl-N-(3-methoxy-2-oxo-1-sulfo-3-azetidinyl)-, (R)- 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Monobactams

Narrower (1)

isosulfazecin

Papers overview

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2006
2006
INTERACTIONS OF FORMYLAMINO-AND METHOXY-SUBSTITUTED ( 3-LACTAM ANTIBIOTICS WITH ( 3-LACTAMASES
Cephem and nocardicin-type monocyclic ,8-lactam antibiotics with a formylamino substituent were highly resistant to hydrolysis by… 
2006
2006
SYNTHESIS OF SULFAZECIN-TYPE 2-AZETIDINONES WITH A CARBON SUBSTITUENT AT THE 4-POSITION
Sir: As reported in our previous paper,1) chemical modification of sulfazecin2) at the 3-position significantly enhanced its… 
2006
2006
A NOVEL ( 3-LACTAM ANTIBIOTIC OF BACTERIAL ORIGIN
Sulfazecin, a new water-soluble acidic antibiotic, which is active against Gram-negative bacteria, was isolated as crystals from… 
1988
1988
MM 42842, a new member of the monobactam family produced by Pseudomonas cocovenenans. II. Production, isolation and properties of MM 42842.
A new member of the monobactam family of beta-lactam antibiotics, designated MM 42842, has been detected in a culture of… 
1985
1985
Chemical modification of sulfazecin. Synthesis of 4-(substituted methyl)-2-azetidinone-1-sulfonic acid derivatives.
In expectation of improving the antibacterial activity of sulfazecin by chemical modification at the 3- and 4-positions, a number… 
1985
1985
Interactions of formylamino- and methoxy-substituted beta-lactam antibiotics with beta-lactamases.
Cephem and nocardicin-type monocyclic beta-lactam antibiotics with a formylamino substituent were highly resistant to hydrolysis… 
1984
1984
Chemical modification of sulfazecin. Synthesis of 4-methoxycarbonyl-2-azetidinone-1-sulfonic acid derivatives.
In the course of the chemical modification of sulfazecin, 3-[2-(2-aminothiazol-4-yl)-(Z)-2-(substituted oxyimino) acetamido]-4… 
1983
1983
Synthesis of sulfazecin-type 2-azetidinones with a carbon substituent at the 4-position.
1983
1983
Synthesis and antibacterial activity of 3-acylamino-3-methoxy-2-azetidinone-1-sulfonic acid derivatives.
As a key intermediate for the synthesis of sulfazecin derivatives, 3-amino-3-methoxy-2-azetidinone (24 or 26) was synthesized… 
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