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)(CCO)CC3)=C(N2C1=O)C([O-])=O

InChIKey

InChIKey=DREMBXJYWSYRSE-KOWPAETKSA-N

Formula

C22H34N4O6S

Mass

482.6

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