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)NCCS(=O)(=O)N(C)CCO)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=UQPQGZFSLUJGFB-PEZGRIKUSA-N

Formula

C20H32N4O8S2

Mass

520.62

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