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](C3)C(=O)NC3=CC=C(CC(O)=O)N3C)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=SMMSCKDIARCUGF-GQMBKMIISA-N

Formula

C22H28N4O7S

Mass

492.55

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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 - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - N-arylamide - Pyrroline carboxylic acid or derivatives - Azepine - N-methylpyrrole - Vinylogous thioester - Dicarboxylic acid or derivatives - Substituted pyrrole - Pyrrole - Heteroaromatic compound - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Azetidine - Secondary alcohol - Thioenolether - Secondary carboxylic acid amide - Amino acid - Tertiary amine - Azacycle - Sulfenyl compound - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Secondary amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Amine - Organic oxide - Organosulfur compound - Organonitrogen compound - Organooxygen compound - 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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