26585-13-7 Usage
Uses
Used in Pharmaceutical Research:
1-Vinyl-4-methoxy-β-carboline is utilized as a research compound for exploring its interactions with the serotonergic system, which is crucial for understanding its potential role in the treatment of neurological and psychiatric disorders.
Used in Cancer Chemoprevention Research:
1-Vinyl-4-methoxy-β-carboline serves as an object of study in cancer chemoprevention, given its potential to impact the development and progression of cancerous cells, making it a candidate for further investigation into its preventive capabilities.
Used in Neurological and Psychiatric Treatment Development:
1-Vinyl-4-methoxy-β-carboline is employed as a potential therapeutic agent in the development of treatments for neurological and psychiatric conditions, leveraging its psychoactive properties and its influence on the serotonergic system.
In the context of different industries, the applications may vary, but based on the provided materials, the primary focus is on the pharmaceutical and medical research sectors for its potential therapeutic and preventive uses.
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 academic research and scientific papers
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.
π-Delocalized β-carbolinium cations as potential antimalarials
Takasu, Kiyosei,Shimogama, Tsubasa,Saiin, Chalerm,Kim, Hye-Sook,Wataya, Yusuke,Ihara, Masataka
, p. 1689 - 1692 (2007/10/03)
Several β-carboline compounds including natural products and their corresponding salts were synthesized and evaluated for antimalarial activity and cytotoxicity levels. Quaternary carbolinium cations showed much higher potencies than neutral β-carbolines
