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Structure Information
Structure

Compound Identification

SMILES

Cl.CC[C@@H]1[C@@H](O)N2[C@H]3C[C@]45C(OC(=O)CCl)C3[C@H]1C[C@H]2[C@@H]4N(C)C1=CC=CC=C51

InChIKey

InChIKey=HNUSYDFQYYRIHJ-XQQGKESMSA-N

Formula

C22H28Cl2N2O3

Mass

439.38

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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 - Beta-carboline - Pyridoindole - Quinolizidine - Indole or derivatives - Dialkylarylamine - Quinuclidine - Tertiary aliphatic/aromatic amine - Azepane - Aralkylamine - Piperidine - Benzenoid - Alpha-halocarboxylic acid derivative - Alpha-halocarboxylic acid or derivatives - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Hemiaminal - Organoheterocyclic compound - Azacycle - Alkanolamine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrochloride - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organochloride - Amine - Organonitrogen compound - Organooxygen compound - Alkyl halide - Alkyl chloride - Organic nitrogen 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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