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](C3)C(=O)NC3=NC(CC(O)=O)=C4NC=NC4=N3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=BOZZFQLOIVSDRO-ZZGPRRSLSA-N

Formula

C22H25N7O7S

Mass

531.54

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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 - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Imidazopyrimidine - Purine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - N-arylamide - Azepine - Dicarboxylic acid or derivatives - Pyrimidine - Vinylogous thioester - Heteroaromatic compound - Tertiary carboxylic acid amide - Imidazole - Azole - Pyrroline - Pyrrolidine - Thioenolether - Tertiary amine - Carboxamide group - Secondary carboxylic acid amide - Azetidine - Amino acid - Amino acid or derivatives - Secondary alcohol - Secondary amine - Secondary aliphatic amine - Carboxylic acid derivative - Sulfenyl compound - Carboxylic acid - Azacycle - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Amine - 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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