77373-72-9 Usage
Description
CHEMBRDG-BB 9071172 is a chemical compound with the molecular formula C23H27NO2, belonging to the indole derivative class and functioning as an inhibitor of the enzyme monoamine oxidase. CHEMBRDG-BB 9071172 holds promise for therapeutic applications, particularly in the treatment of neurological and psychiatric disorders such as depression and anxiety, as well as potential use in cancer research due to its observed anti-cancer properties.
Uses
Used in Pharmaceutical Industry:
CHEMBRDG-BB 9071172 is used as a therapeutic agent for the treatment of neurological and psychiatric disorders, specifically targeting depression and anxiety. Its mechanism of action involves inhibiting the enzyme monoamine oxidase, which plays a crucial role in the regulation of neurotransmitters and mood.
Used in Cancer Research:
In the field of cancer research, CHEMBRDG-BB 9071172 is used for its potential anti-cancer properties. Further studies are required to explore its efficacy and the mechanisms through which it may contribute to cancer treatment or prevention.
Check Digit Verification of cas no
The CAS Registry Mumber 77373-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77373-72:
(7*7)+(6*7)+(5*3)+(4*7)+(3*3)+(2*7)+(1*2)=159
159 % 10 = 9
So 77373-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNO/c1-6-8-4-7(11)2-3-9(8)12-10(6)5-13/h2-4,12-13H,5H2,1H3
77373-72-9Relevant articles and documents
Synthesis & Reaction of Indole-1,2-dicarboxaldehydes with Hydrazine & Hydroxylamine
Hiremath, Shivayogi P.,Thakar, Shreeram B.,Purohit, Muralidhar G.
, p. 770 - 774 (2007/10/02)
Indole-1,2-dicarboxaldehydes (2a-g) have been prepared by formylation of 3-methylindole-2-carboxaldehydes (1a-g) with DMF-POCl3 at 140 deg C. 2a-e react with N2H4.H2O to give hydrazones (3a-e and 3g) of 1-formylindole-2-carboxaldehydes instead of the tria
