26585-13-7 Usage
General Description
1-Vinyl-4-methoxy-β-carboline is a chemical compound with a molecular formula C14H12N2O. It is a derivative of the naturally occurring alkaloid β-carboline, and is known for its psychoactive properties. 1-Vinyl-4-methoxy-β-carboline has been studied for its potential pharmacological effects, including its interactions with the serotonergic system and its potential use in the treatment of neurological and psychiatric disorders. It has also been investigated for its potential as a cancer chemopreventive agent. 1-Vinyl-4-methoxy-β-carboline has been synthesized in laboratory settings for research purposes, and its structure and properties have been characterized using various spectroscopic techniques. Its synthesis and potential applications continue to be the subject of ongoing scientific research.
Check Digit Verification of cas no
The CAS Registry Mumber 26585-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,8 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26585-13:
(7*2)+(6*6)+(5*5)+(4*8)+(3*5)+(2*1)+(1*3)=127
127 % 10 = 7
So 26585-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O/c1-3-10-14-13(12(17-2)8-15-10)9-6-4-5-7-11(9)16-14/h3-8,16H,1H2,2H3
26585-13-7Relevant articles and documents
Synthesis and evaluation of β-carbolinium cations as new antimalarial agents based on π-delocalized lipophilic cation (DLC) hypothesis
Takasu, Kiyosei,Shimogama, Tsubasa,Saiin, Chalerm,Kim, Hye-Sook,Wataya, Yusuke,Brun, Reto,Ihara, Masataka
, p. 653 - 661 (2007/10/03)
Several β-carbolines including naturally occurring substances and their corresponding cationic derivatives were synthesized and evaluated for antimalarial (antiplasmodial) activity in vitro and in vivo. A tetracyclic carbolinium salt was elucidated for antileishmanial and antitrypanosomal activities in vitro as well as antiplasmodial activity. Quarternary carbolinium cations showed much higher potencies in vitro than electronically neutral β-carbolines and a good correlation was observed between π-delocalized lipophilic cationic (DLC) structure and antimalarial efficacy. β-Carbolinium compounds exhibit medium suppressive activity in vivo against rodent malaria.
