Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=CSC(C[C@@H]2C[C@@H](CN2C(=O)OCC2=CC=C(C=C2)[N+]([O-])=O)SC2=C(N3C(C([C@@H](C)O)C3=O)[C@H]2C)C(=O)OCC2=CC=C(C=C2)[N+]([O-])=O)=N1

InChIKey

InChIKey=DLGBAUDRNUYUII-AFPRICBLSA-N

Formula

C36H37N5O12S2

Mass

795.84

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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 - Nitroaromatic compound - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Thiazolecarboxylic acid or derivatives - 2,4-disubstituted 1,3-thiazole - Azepine - Monocyclic benzene moiety - Vinylogous thioester - Benzenoid - Azole - Heteroaromatic compound - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Thiazole - Carbamic acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Secondary alcohol - Thioenolether - Azetidine - Carboxamide group - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic oxoazanium - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organic salt - Organic zwitterion - Alcohol - 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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