Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@H](CNC(=O)C4=CC(=O)C(O)=CN4O)C3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=CREQWXYYMFVKTM-GDGCIOESSA-N

Formula

C21H26N4O8S

Mass

494.52

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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 - Alpha-amino acid or derivatives - Pyridine carboxylic acid or derivatives - 2-heteroaryl carboxamide - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Azepine - Dihydropyridine - Hydroxypyridine - Hydropyridine - Pyridine - Vinylogous thioester - Tertiary carboxylic acid amide - Heteroaromatic compound - Pyrrolidine - Vinylogous amide - Pyrroline - Amino acid or derivatives - Azetidine - Carboxamide group - Amino acid - Cyclic ketone - Thioenolether - Secondary carboxylic acid amide - Secondary alcohol - Secondary amine - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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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