Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN(C3)C3=NCCN3CC3=CC=C(CN)C=C3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=KVPTWVBTRXTIQF-TWKYDXJASA-N

Formula

C24H31N5O4S

Mass

485.6

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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 - Benzylamine - Phenylmethylamine - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Aralkylamine - Monocyclic benzene moiety - Vinylogous thioester - Benzenoid - 2-imidazoline - Pyrroline - Tertiary carboxylic acid amide - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Guanidine - Secondary alcohol - Thioenolether - Azacycle - Carboximidamide - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Carboxylic acid derivative - Carboxylic acid - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Amine - Organic oxide - Primary amine - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organosulfur 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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