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

InChIKey=BTBWJWNOSNFGSG-ARDYCFFISA-N

C29H25N7O5S2

615.68

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Not available

Carbacephems

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

Aromatic heteropolycyclic compounds

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