Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@H](N(C)C3)C(=O)N3CC[C@H](N)C3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=VQPULULJDGLWBN-UBRSESRLSA-N

Formula

C20H30N4O5S

Mass

438.54

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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 - Alpha-amino acid amide - Alpha-amino acid or derivatives - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - N-alkylpyrrolidine - Vinylogous thioester - Pyrrolidine - Tertiary carboxylic acid amide - Pyrroline - Carboxamide group - Azetidine - Amino acid or derivatives - Amino acid - Tertiary aliphatic amine - Secondary alcohol - Tertiary amine - Thioenolether - Carboxylic acid - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxide - Primary aliphatic amine - Alcohol - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Primary amine - Organic nitrogen compound - Organic oxygen compound - Amine - 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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