Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2CC(SCCN=CN)=C(N2C1=O)C(O)=O.OC(=O)C1=C(CS[C@@H]2[C@H](NC(=O)CSC3=CC=CC=C3)C(=O)N12)\C=C1/CCN(CC2=CC=[N+](CC(=O)NC3=CC(F)=C(O)C=C3)C=C2)C1=O

InChIKey

InChIKey=ULRWIFOAKUKSGV-HDKATYIYSA-O

Formula

C46H48FN8O11S3

Mass

1004.11

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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

Not available

Substituents

Thienamycin - Cephalosporin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Cephem - Anilide - 2-halophenol - Aryl thioether - 2-fluorophenol - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Thiophenol ether - N-arylamide - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Fluorobenzene - Halobenzene - Azepine - Alkylarylthioether - Vinylogous thioester - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - N-alkylpyrrolidine - Meta-thiazine - Pyridine - Pyridinium - Pyrrolidone - 2-pyrrolidone - Benzenoid - Heteroaromatic compound - Tertiary carboxylic acid amide - Pyrrolidine - Pyrroline - Secondary carboxylic acid amide - Secondary alcohol - Thioenolether - Azetidine - Carboxamide group - Azacycle - Sulfenyl compound - Carboximidamide - Dialkylthioether - Hemithioaminal - Thioether - Carboxylic acid amidine - Carboxylic acid derivative - Carboxylic acid - Formamidine - Amidine - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Imine - Alcohol - Organic nitrogen compound - Organohalogen compound - Organofluoride - 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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