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Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@H]1[C@@H]2[C@H](C)C(S[C@@H]3C[NH2+][C@@H](C3)C(=O)N(C)C)=C(N2C1=O)C([O-])=O

InChIKey

InChIKey=DMJNNHOOLUXYBV-XFVKVHEMSA-N

Formula

C17H25N3O5S

Mass

383.46

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