Structure Information
Structure

Compound Identification

SMILES

CN1C(=CN=C1C1=NC(=CS1)C1=C(N2[C@H](CC1)[C@H](NC(=O)C(=NO)C1=CSC(N)=N1)C2=O)C(O)=O)[N+]([O-])=O

InChIKey

InChIKey=ARVNBMZBKRPKEA-MFKMUULPSA-N

Formula

C20H17N9O7S2

Mass

559.53

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