Structure Information
Structure

Compound Identification

SMILES

CC[C@@H]1[C@@H](O)N2[C@H]3CC45C(OC(=O)C6=CC(OC)=C(OC)C(OC)=C6)C3C1C[C@H]2[C@@H]4N(C)C1=CC=CC=C51

InChIKey

InChIKey=JCRQPLRRHXVYJF-DBROWAFRSA-N

Formula

C30H36N2O6

Mass

520.626

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Ajmaline-sarpagine alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Ajmaline-sarpagine alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Sarpagine-skeleton - Pyridoindole - Beta-carboline - Gallic acid or derivatives - M-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Quinolizidine - Benzoate ester - Indole or derivatives - Benzoic acid or derivatives - Benzoyl - Methoxybenzene - Tertiary aliphatic/aromatic amine - Quinuclidine - Phenoxy compound - Anisole - Phenol ether - Dialkylarylamine - Azepane - Alkyl aryl ether - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Piperidine - Hemiaminal - Amino acid or derivatives - Tertiary amine - Carboxylic acid ester - Alkanolamine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as ajmaline-sarpagine alkaloids. These are organic compounds containing either of the ajmalan, sarpagan skeleton, or derivative thereof. The Sarpagine (Akuammidine) group, based on the sarpagan nucleus, arises from bond formation between C-16 and C-5 of the corynantheine precursor. Ajmaline alkaloids are based on a 17,19-secoyohimban skeleton (oxayohimban) which is invariably present as an ether.

External Descriptors

Not available

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