Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@@H](CC4CN[C@@H](C4)C(=O)NC(=O)OCC=C)N(C3)C(=O)OCC=C)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=JMPYCBIHIPTEAB-DPFKMHKNSA-N

Formula

C28H38N4O9S

Mass

606.69

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