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=CC4=C(N)C=C(CC(O)=O)C=C4S3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=CWMTWJCLUXIFQW-GXISVTECSA-N

Formula

C25H28N4O7S2

Mass

560.64

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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 - Benzothiophene - 1-benzothiophene - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - N-arylamide - 2,3,5-trisubstituted thiophene - Azepine - Dicarboxylic acid or derivatives - Benzenoid - Vinylogous thioester - Thiophene - Tertiary carboxylic acid amide - Pyrrolidine - Heteroaromatic compound - Pyrroline - Amino acid or derivatives - Carboxamide group - Azetidine - Amino acid - Thioenolether - Tertiary amine - Secondary alcohol - Secondary carboxylic acid amide - Secondary aliphatic amine - Carboxylic acid - Azacycle - Sulfenyl compound - Secondary amine - Carboxylic acid derivative - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - Organosulfur compound - Primary amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - 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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