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)NC3=CC=CC(=C3)C(O)=O)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=ZXNAQFZBWUNWJM-HRXMHBOMSA-N

Formula

C22H25N3NaO7S

Mass

498.51

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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

Aromatic heteropolycyclic compounds

Substituents

Thienamycin - Acylaminobenzoic acid or derivatives - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Benzoic acid or derivatives - Benzoic acid - Anilide - Benzoyl - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - N-arylamide - Azepine - Monocyclic benzene moiety - Vinylogous thioester - Benzenoid - Pyrroline - Tertiary carboxylic acid amide - Pyrrolidine - Secondary carboxylic acid amide - Thioenolether - Secondary alcohol - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Sulfenyl compound - Secondary amine - Organic alkali metal salt - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Alcohol - Carbonyl group - Organosulfur compound - Organic oxygen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic cation - Aromatic 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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