Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)C1C2[C@@H](C)C(SC3CN(C3)C3=NC(CNC(=O)C4=CC=CC=C4)=CS3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=PCZWNCMGCFKSRC-LGBHXNNWSA-N

Formula

C24H26N4O5S2

Mass

514.62

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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

Aromatic heteropolycyclic compounds

Substituents

Thienamycin - Alpha-amino acid or derivatives - Benzamide - Benzoic acid or derivatives - Benzoyl - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Dialkylarylamine - Azepine - 2,4-disubstituted 1,3-thiazole - Benzenoid - 1,3-thiazol-2-amine - Vinylogous thioester - Monocyclic benzene moiety - Heteroaromatic compound - Thiazole - Tertiary carboxylic acid amide - Pyrroline - Azole - Thioenolether - Secondary carboxylic acid amide - Secondary alcohol - Azetidine - Carboxamide group - Azacycle - Sulfenyl compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Organic oxide - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Alcohol - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Amine - Hydrocarbon derivative - Aromatic 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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