Structure Information
Structure

Compound Identification

SMILES

CC(C)OC(=O)OC(C)OC(=O)C1=C(SC2CNC(=O)C2)[C@H](C)C2C([C@@H](C)OC(=O)CN)C(=O)N12

InChIKey

InChIKey=LZGNIMBRUJUWAX-BJSXLXPESA-N

Formula

C22H31N3O9S

Mass

513.56

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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 ester - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Carbonic acid diester - Dicarboxylic acid or derivatives - Vinylogous thioester - Pyrrolidone - 2-pyrrolidone - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tertiary carboxylic acid amide - Pyrroline - Amino acid or derivatives - Azetidine - Carboxamide group - Carboxylic acid ester - Carbonic acid derivative - Thioenolether - Secondary carboxylic acid amide - Acetal - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organosulfur compound - Primary amine - Primary aliphatic amine - Amine - Organonitrogen 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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