Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=UBQRNADYCUXRBD-WJEFCNIMSA-M

Formula

C17H24N3NaO5S

Mass

405.44

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