Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=WTDVGWSROFPHDP-RIRUNEHBSA-N

Formula

C23H19N7O7S2

Mass

569.57

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Lactams

Subclass

Beta lactams

Intermediate Tree Nodes

Not available

Direct Parent

Carbacephems

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Carbacephem - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Nitrobenzene - Nitroaromatic compound - 2,4-disubstituted 1,3-thiazole - Tetrahydropyridine - 1,3-thiazol-2-amine - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Tertiary carboxylic acid amide - Azole - Thiazole - Amino acid or derivatives - C-nitro compound - Amino acid - Carboxamide group - Azetidine - Secondary carboxylic acid amide - Organic nitro compound - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxoazanium - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Primary amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

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.

External Descriptors

Not available

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