Structure Information
Structure

Compound Identification

SMILES

OC1=C(C=C(C=C1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O.COC1=C(OC)C=C2C(=C1)N1CCC3OCCC4CN5CCC22C5CC4C3C12

InChIKey

InChIKey=FCKNYTHTWLUCIC-UHFFFAOYSA-N

Formula

C29H33N5O10

Mass

611.608

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Strychnos alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Strychnos alkaloids

Alternative Parents

Molecular Framework

Not available

Substituents

Strychnan skeleton - Akuammicine-skeleton - Stemmadenine-skeleton - Carbazole - Quinolidine - Nitrophenol - Nitrobenzene - Indolizidine - Indole or derivatives - Nitroaromatic compound - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Anisole - Aralkylamine - Phenol - Oxepane - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Piperidine - Monocyclic benzene moiety - Pyrrolidine - Organic nitro compound - Tertiary aliphatic amine - Tertiary amine - C-nitro compound - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

External Descriptors

Not available

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