Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](\C=C\C2=CC=CC=C2)N(\C(=C\SCCCSSCCCS\C=C(/C=N/NC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)\N2[C@H](\C=C\C3=CC=CC=C3)[C@H](OC)C2=O)\C=N\NC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)C1=O

InChIKey

InChIKey=VZQXTARFPBADSG-RMJYUACZSA-N

Formula

C48H48N10O12S4

Mass

1085.21

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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 - Nitrobenzene - Nitroaromatic compound - Phenylhydrazine - Styrene - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - C-nitro compound - Organic nitro compound - Dialkyldisulfide - Carboxamide group - Organic disulfide - Azetidine - Thioenolether - Sulfenyl compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Dialkyl ether - Ether - Hydrazone - Organic oxoazanium - Organic 1,3-dipolar compound - Azacycle - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic zwitterion - Organic salt - Carbonyl group - Hydrocarbon derivative - 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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