Structure Information
Structure

Compound Identification

SMILES

[Na+].CON=C(C(=O)N[C@@H]1[C@@H](N(C1=O)S([O-])(=O)=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O)C1=CSC(N)=N1

InChIKey

InChIKey=JWVJUMWQPOMYHE-OJERSXHUSA-M

Formula

C17H15N6NaO10S2

Mass

550.45

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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 - Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - 2,4-disubstituted 1,3-thiazole - Azetidinecarboxylic acid - Monocyclic benzene moiety - 1,3-thiazol-2-amine - Benzenoid - Organic sulfuric acid or derivatives - Heteroaromatic compound - Thiazole - Azole - C-nitro compound - Azetidine - Secondary carboxylic acid amide - Organic nitro compound - Carboxylic acid ester - Carboxamide group - Amino acid or derivatives - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Organic alkali metal salt - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Primary amine - Organic zwitterion - Organic salt - Organic sodium salt - Hydrocarbon derivative - Amine - Organic oxide - 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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