Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1C(O)[C@H](O[C@@H](CO[C@@H]2[C@H](N(C2=O)C2=CC=CC=C2)C2=C(O)C=C(C=C2)C2=CC(O)=CC=C2)C2=CC=C(F)C=C2)OC([C@@H]1O)C(O)=O

InChIKey

InChIKey=QFBAWKNFBAURFV-UIXFRUJCSA-N

Formula

C35H32FNO11

Mass

661.635

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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 - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Biphenyl - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - 2-phenylazetidine - 1-phenylazetidine - Beta-hydroxy acid - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Fluorobenzene - Halobenzene - Phenol - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Hydroxy acid - Benzenoid - Monosaccharide - Pyran - Oxane - Tertiary carboxylic acid amide - Azetidine - Secondary alcohol - Carboxamide group - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Oxacycle - Azacycle - Acetal - Organooxygen compound - Alcohol - Carbonyl group - Organonitrogen compound - Organofluoride - Organohalogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen 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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