CO\N=C(\C(=O)N[C@H]1[C@H]2CCC(\C=C\C3=C(C)SC=N3)=C(N2C1=O)C(O)=O)C1=CSC(N)=N1

InChIKey=NZLNZQGQXWKUCK-JFUOAMSESA-N

C20H20N6O5S2

488.54

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Not available

Carbacephems

N-acyl-alpha amino acids and derivatives Tetrahydropyridines 2,4-disubstituted thiazoles 4,5-disubstituted thiazoles 2-amino-1,3-thiazoles Tertiary carboxylic acid amides Heteroaromatic compounds Tertiary amines Secondary carboxylic acid amides Amino acids Azetidines Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Primary amines

Aromatic heteropolycyclic compounds

Carbacephem - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - 2,4-disubstituted 1,3-thiazole - 4,5-disubstituted 1,3-thiazole - Tetrahydropyridine - 1,3-thiazol-2-amine - Azole - Tertiary carboxylic acid amide - Heteroaromatic compound - Thiazole - Tertiary amine - Secondary carboxylic acid amide - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Primary amine - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as carbacephems. These are a new class of beta-lactam antibiotics similar in structure to the cephalosporins. They differ from cephalosporins, however, in the substitution of a sulfur atom in the dihydrothiazine ring with a methylene group to form a tetrahydropyridine ring.

Not available