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Structure Information
Structure

Compound Identification

SMILES

C[C@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3C[NH2+][C@H](CNS(N)(=O)=O)C3)=C(N2C1=O)C([O-])=O

InChIKey

InChIKey=AVAACINZEOAHHE-BAMVVWIKSA-N

Formula

C15H24N4O6S2

Mass

420.5

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Lactams

Subclass

Beta lactams

Intermediate Tree Nodes

Carbapenems

Direct Parent

Thienamycins

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Sulfuric acid diamide - Vinylogous thioester - Organic sulfuric acid or derivatives - Pyrrolidine - Pyrroline - Quaternary ammonium salt - Tertiary carboxylic acid amide - Amino acid or derivatives - Tertiary amine - Secondary alcohol - Thioenolether - Azetidine - Carboxamide group - Amino acid - Carboxylic acid salt - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as thienamycins. These are beta-lactam antibiotics that differ from penicillins in having the thiazolidine sulfur atom replaced by carbon, the sulfur then becoming the first atom in the side chain.

External Descriptors

Not available

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