Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CN2[C@H](CC(=O)S[C@H]3CCN(C3)C(\C)=N\C(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)[C@@H]([C@@H](C)OC(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)C2=O)C=C1

InChIKey

InChIKey=YTBAWGZCLFTOJJ-PIOZAUNISA-N

Formula

C37H39N5O12S

Mass

777.8

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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 - Benzyloxycarbonyl - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Carbonic acid diester - Pyrrolidine - Tertiary carboxylic acid amide - Organic nitro compound - C-nitro compound - Carbonic acid derivative - Azetidine - Carboxamide group - Thiocarboxylic acid ester - Carbothioic s-ester - Amidine - Azacycle - Carboxylic acid amidine - Organic 1,3-dipolar compound - Carboxylic acid derivative - Ether - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Sulfenyl compound - Organic oxoazanium - Carboximidamide - Thiocarboxylic acid or derivatives - Hydrocarbon derivative - Organic nitrogen compound - Organic salt - Organic zwitterion - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - 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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