Structure Information
Structure

Compound Identification

SMILES

C[C@@H](CC[C@@H]1[C@H](N(C1=O)C1=CC=C(F)C=C1)C1=CC=C(C=C1)C1=CC=C(C=C1)S(=O)(=O)C[C@@H]1OC(CO)[C@@H](O[C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)[C@H](O)C1O)C1=CC=C(F)C=C1

InChIKey

InChIKey=GMXDSFQUCNLMNN-AIYHLGAKSA-N

Formula

C44H49F2NO13S

Mass

869.93

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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 - Biphenyl - O-glycosyl compound - Glycosyl compound - Disaccharide - C-glycosyl compound - 1-phenylazetidine - 2-phenylazetidine - Benzenesulfonyl group - Fluorobenzene - Halobenzene - Benzenoid - Oxane - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Sulfonyl - Sulfone - Azetidine - Carboxamide group - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Polyol - Organic nitrogen compound - Organofluoride - Organonitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Primary alcohol - Organopnictogen compound - Organosulfur compound - Organohalogen 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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