Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN(C3)C3=NC(=CO3)C(=O)N3CCOCC3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=CYRDJVOZSKRNAT-YIKOMLBNSA-N

Formula

C21H26N4O7S

Mass

478.52

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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 - Morpholine-4-carboxylic acid or derivatives - 2-heteroaryl carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Dialkylarylamine - 2,4-disubstituted 1,3-oxazole - Azepine - Morpholine - Oxazinane - Vinylogous thioester - Azole - Oxazole - Heteroaromatic compound - Pyrroline - Tertiary carboxylic acid amide - Thioenolether - Secondary alcohol - Azetidine - Carboxamide group - Azacycle - Sulfenyl compound - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organic oxide - Organooxygen compound - Amine - 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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