Structure Information
Structure

Compound Identification

SMILES

CC(O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@]3(CNC(=O)C3)C(=O)N3CCN(CC(=O)OCC4=CC=C(C=C4)[N+]([O-])=O)CC3)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=APUUSVHMBMNCHG-YZDNTSIVSA-N

Formula

C28H33N5O10S

Mass

631.66

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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 ester - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Pyrroline carboxylic acid - Nitroaromatic compound - Pyrrolidine-3-carboxamide - Pyrrolidine carboxylic acid or derivatives - Pyrroline carboxylic acid or derivatives - Azepine - N-alkylpiperazine - Piperazine - Benzenoid - Monocyclic benzene moiety - Pyrrolidone - 2-pyrrolidone - Dicarboxylic acid or derivatives - Vinylogous thioester - 1,4-diazinane - Tertiary carboxylic acid amide - Pyrrolidine - Pyrroline - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Tertiary aliphatic amine - Thioenolether - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Azacycle - Sulfenyl compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Organic oxoazanium - Amine - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Carbonyl group - Organic salt - Organic oxide - Organic zwitterion - Hydrocarbon derivative - 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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