Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@H](N(C3)C(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)C(=O)N3CC[S+](C)CC3)=C(N2C1=O)C(=O)OC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=KHIDGTHYHXIZNS-CCCPLFPKSA-N

Formula

C34H38N5O11S2

Mass

756.82

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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 amide - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Phenol ester - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrrolidine-2-carboxamide - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Azepine - Vinylogous thioester - Monocyclic benzene moiety - 1,4-thiazinane - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Pyrrolidine - Carbamic acid ester - Pyrroline - Tertiary carboxylic acid amide - Thioenolether - Azetidine - Secondary alcohol - Carboxamide group - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Organic oxoazanium - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic salt - Hydrocarbon derivative - Alcohol - Organic oxide - 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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