2134-82-9 Usage
Chemical classification
Belongs to the vobasane group, a type of indole alkaloid.
Source
Derived from the Tabernaemontana divaricata plant.
Medicinal properties
Possesses potential medicinal properties.
Anti-inflammatory activity
Has shown anti-inflammatory properties in various studies.
Antimalarial activity
Exhibits antimalarial properties.
Cytotoxic activity
Demonstrates cytotoxic activities.
Neurological disorders
Investigated for its potential in treating neurological disorders such as Alzheimer's disease.
Structural features
The structural features of 17-Hydroxyvobasan-3-one contribute to its biological activities.
Research interest
An interesting target for further research in the field of drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 2134-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2134-82:
(6*2)+(5*1)+(4*3)+(3*4)+(2*8)+(1*2)=59
59 % 10 = 9
So 2134-82-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H24N2O2/c1-3-12-10-22(2)18-8-15-13-6-4-5-7-17(13)21-20(15)19(24)9-14(12)16(18)11-23/h3-7,14,16,18,21,23H,8-11H2,1-2H3/b12-3-/t14-,16?,18-/m1/s1
2134-82-9Relevant articles and documents
The first enantiospecific total synthesis of the 3-oxygenated sarpagine indole alkaloids affinine and 16-epiaffinine, as well as vobasinediol and 16-epivobasinediol
Yang, Jie,Rallapalli, Sundari K.,Cook, James M.
scheme or table, p. 815 - 817 (2010/03/26)
The first enantiospecific total synthesis of the 3-oxygenated sarpagine indole alkaloids affinine (1) and 16-epiaffinine (2) as well as the synthesis of vobasinediol (3) and 16-epivobasinediol (4) was accomplished from d-(+)-tryptophan methyl ester.
