Structure Information
Structure

Compound Identification

SMILES

CCSC([C@@H]1C[C@@H](CN1)SC1=C(N2[C@@H]([C@@H]([C@@H](C)O)C2=O)[C@H]1C)C(O)=O)C(=O)N(N)CC

InChIKey

InChIKey=ATTAVIYNHMJHPS-KDBYIVBFSA-N

Formula

C20H32N4O5S2

Mass

472.62

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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 - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Carboxylic acid hydrazide - Carboxamide group - Azetidine - Amino acid or derivatives - Secondary alcohol - Tertiary amine - Amino acid - Thioenolether - Dialkylthioether - Monocarboxylic acid or derivatives - Sulfenyl compound - Carboxylic acid derivative - Secondary amine - Carboxylic acid - Secondary aliphatic amine - Azacycle - Thioether - Organic oxide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organosulfur compound - Alcohol - Amine - Organic nitrogen compound - Hydrocarbon derivative - 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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