CCN1CCC(N(C=O)C(C(=O)N[C@H]2[C@H]3CCC(Cl)=C(N3C2=O)C(O)=O)C2=CC=C(O)C=C2)C(=O)C1=O

InChIKey=MOUPGIRSIXDSAH-ZLZJIPBDSA-N

C24H25ClN4O8

532.93

Organic compounds

Organoheterocyclic compounds

Lactams

Beta lactams

Not available

Carbacephems

N-acyl-alpha amino acids and derivatives Phenylacetamides Piperidinediones 1-hydroxy-2-unsubstituted benzenoids Tetrahydropyridines Delta lactams Vinylogous halides Tertiary carboxylic acid amides Azetidines Cyclic ketones Secondary carboxylic acid amides Monocarboxylic acids and derivatives Vinyl chlorides Azacyclic compounds Chloroalkenes Carboxylic acids Hydrocarbon derivatives Organonitrogen compounds Organic oxides Organochlorides

Aromatic heteropolycyclic compounds

Carbacephem - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Phenylacetamide - Piperidinedione - 1-hydroxy-2-unsubstituted benzenoid - Delta-lactam - Phenol - Piperidinone - Tetrahydropyridine - Monocyclic benzene moiety - Piperidine - Benzenoid - Vinylogous halide - Tertiary carboxylic acid amide - Cyclic ketone - Secondary carboxylic acid amide - Azetidine - Carboxamide group - Ketone - Vinyl chloride - Haloalkene - Vinyl halide - Carboxylic acid derivative - Carboxylic acid - Chloroalkene - Monocarboxylic acid or derivatives - Azacycle - Organic oxide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - 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