Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)N([C@@H]1[C@H](OC2=CC=CC=C2)C(=O)N1C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=GVRHUEMPEFJHOH-RRPNLBNLSA-N

Formula

C28H24N2O4S

Mass

484.57

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Lactams

Subclass

Beta lactams

Intermediate Tree Nodes

Not available

Direct Parent

Monobactams

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Monobactam - N,n-disubstituted p-toluenesulfonamide - P-toluenesulfonamide - Benzenesulfonamide - 1-phenylazetidine - Sulfanilide - Tosyl compound - Benzenesulfonyl group - Phenoxy compound - Phenol ether - Alkyl aryl ether - Toluene - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid amide - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Sulfonyl - Tertiary carboxylic acid amide - Aminosulfonyl compound - Carboxamide group - Azetidine - Azacycle - Carboxylic acid derivative - Ether - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as monobactams. These are compounds comprising beta-lactam ring is alone and not fused to another ring.

External Descriptors

Not available

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