865187-17-3 Usage
Description
16-epi-Nb-Methylvoacarpine is a chemical compound belonging to the Iboga alkaloid family, derived from the leaves of the Voacanga africana plant. It exhibits psychoactive properties and has garnered attention for its potential therapeutic applications in various neurological disorders, addiction treatment, and pain management.
Used in Pharmaceutical Industry:
16-epi-Nb-Methylvoacarpine is used as a potential treatment for neurological disorders such as Parkinson's disease and Alzheimer's disease, due to its psychoactive properties and potential neuroprotective effects.
Used in Addiction Treatment:
16-epi-Nb-Methylvoacarpine is used as a potential therapeutic agent for addiction and substance abuse treatment, leveraging its psychoactive properties to aid in recovery and rehabilitation processes.
Used in Pain Management:
16-epi-Nb-Methylvoacarpine is used as an anti-inflammatory and analgesic agent, with its potential to alleviate pain and reduce inflammation being of interest to researchers and pharmaceutical companies.
Used in Research:
16-epi-Nb-Methylvoacarpine is used as a subject of study for its unique structure and potential therapeutic applications, with researchers and pharmaceutical companies exploring its mechanisms of action and efficacy in various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 865187-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,1,8 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 865187-17:
(8*8)+(7*6)+(6*5)+(5*1)+(4*8)+(3*7)+(2*1)+(1*7)=203
203 % 10 = 3
So 865187-17-3 is a valid CAS Registry Number.
865187-17-3Relevant articles and documents
Six new indole alkaloids from Gelsemium sempervirens Ait. f.
Kogure, Noriyuki,Nishiya, Chika,Kitajima, Mariko,Takayama, Hiromitsu
, p. 5857 - 5861 (2007/10/03)
One new yohimbane and five new sarpagine-type indole alkaloids were isolated from the radix of Gelsemium sempervirens Ait. f., and their structures were determined by spectroscopic analysis, chemical conversion or total synthesis. It was found that 2-acyl sarpagine-type alkaloids possessing an Nb-methyl group take a keto-amino structure or a transannular form in solution depending on the solvent.
