Structure Information
Structure

Compound Identification

SMILES

CNCCC(O)C1CC(CN1)SC1=C(N2C(C(C(C)O)C2=O)C1C)C(O)=O

InChIKey

InChIKey=PZLOCBSBEUDCPF-UHFFFAOYSA-N

Formula

C18H29N3O5S

Mass

399.51

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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 or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - 1,3-aminoalcohol - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - 1,2-aminoalcohol - Amino acid or derivatives - Azetidine - Carboxamide group - Amino acid - Secondary alcohol - Thioenolether - Secondary amine - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Carbonyl group - Alcohol - Organic oxide - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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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