Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@H](CNC(=O)C4=CC(O)=C(O)C=C4)C3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=OZODHKMJGWUQMX-GQMBKMIISA-N

Formula

C22H27N3O7S

Mass

477.53

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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 - Catechol - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous thioester - Benzenoid - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Pyrrolidine - Pyrroline - Secondary alcohol - Azetidine - Thioenolether - Carboxamide group - Secondary carboxylic acid amide - Amino acid - Amino acid or derivatives - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Secondary amine - Carboxylic acid - Carboxylic acid derivative - Azacycle - Sulfenyl compound - Organic nitrogen compound - Alcohol - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Amine - 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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