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)N3CC[N+](C)(CC(N)=O)CC3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=DQCNSUXWAHEDCP-DUUYBOGCSA-O

Formula

C22H34N5O6S

Mass

496.6

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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

Aliphatic heteropolycyclic compounds

Substituents

Thienamycin - Alpha-amino acid amide - Alpha-amino acid or derivatives - N-piperazineacetamide - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - N-alkylpiperazine - N-methylpiperazine - 1,4-diazinane - Vinylogous thioester - Piperazine - Tetraalkylammonium salt - Pyrrolidine - Pyrroline - Quaternary ammonium salt - Tertiary carboxylic acid amide - Primary carboxylic acid amide - Thioenolether - Azetidine - Amino acid - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Sulfenyl compound - Monocarboxylic acid or derivatives - Secondary amine - Organic nitrogen compound - Carbonyl group - Alcohol - Organic oxygen compound - Amine - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic cation - 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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