Structure Information
Structure

Compound Identification

SMILES

CC(=O)NCCS(=O)C1=C(N2[C@H](C1)[C@H](C2=O)C(C)(C)OC(=O)OCC1=CC=C(C=C1)[N+]([O-])=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=UDYDLLNKLIELJA-QDJXSUPSSA-N

Formula

C29H30N4O12S

Mass

658.64

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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 - Benzyloxycarbonyl - Nitrobenzene - Pyrroline carboxylic acid or derivatives - Nitroaromatic compound - Pyrroline carboxylic acid - Azepine - Monocyclic benzene moiety - Carbonic acid diester - Benzenoid - Acetamide - Tertiary carboxylic acid amide - Pyrroline - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carbonic acid derivative - Secondary carboxylic acid amide - Organic nitro compound - Sulfoxide - Azetidine - Carboxamide group - Carboxylic acid ester - C-nitro compound - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Sulfinyl compound - Organopnictogen compound - Organic oxygen compound - Organic salt - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - 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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