Structure Information
Structure

Compound Identification

SMILES

CO\N=C(\C(=O)N[C@H]1[C@H]2CCC(C3=CSC(=N3)C3=NC=C(S3)[N+]([O-])=O)=C(N2C1=O)C(O)=O)C1=CSC(N)=N1

InChIKey

InChIKey=ZQHRMOJEKQFKEP-DTXIJPRKSA-N

Formula

C20H16N8O7S3

Mass

576.58

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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 - Nitroaromatic compound - Nitrothiazole - 2,4-disubstituted 1,3-thiazole - 2,5-disubstituted 1,3-thiazole - Tetrahydropyridine - 1,3-thiazol-2-amine - Azole - Heteroaromatic compound - Tertiary carboxylic acid amide - Thiazole - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic 1,3-dipolar compound - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Organooxygen compound - Organic nitrogen compound - Amine - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary amine - Organic oxygen compound - Organic salt - Organonitrogen compound - Organic zwitterion - 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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