249762-74-1 Usage
Uses
Used in Pharmaceutical Industry:
(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE is used as a research chemical for studying the effects of psychedelic substances on the human brain and their potential therapeutic applications. Its ability to act as a serotonin receptor agonist makes it a valuable tool in understanding the role of serotonin in various neurological and psychiatric disorders.
Used in Research and Development:
(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE is used as a research compound in the development of new drugs and therapies targeting the serotonin system. Its psychoactive properties and structural similarity to serotonin make it a useful starting point for designing new molecules with potential therapeutic benefits.
Used in Forensic Science:
(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE is used as a reference compound in forensic science for the identification and analysis of controlled substances, particularly in cases involving drug abuse and illegal drug trafficking.
Check Digit Verification of cas no
The CAS Registry Mumber 249762-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,9,7,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 249762-74:
(8*2)+(7*4)+(6*9)+(5*7)+(4*6)+(3*2)+(2*7)+(1*4)=181
181 % 10 = 1
So 249762-74-1 is a valid CAS Registry Number.
249762-74-1Relevant academic research and scientific papers
Bis(1H-2-indolyl)methanones as a novel class of inhibitors of the platelet-derived growth factor receptor kinase
Mahboobi, Siavosh,Teller, Steffen,Pongratz, Herwig,Hufsky, Harald,Sellmer, Andreas,Botzki, Alexander,Uecker, Andrea,Beckers, Thomas,Baasner, Silke,Sch?chtele, Christoph,überall, Florian,Kassack, Matthias U.,Dove, Stefan,B?hmer, Frank-D.
, p. 1002 - 1018 (2007/10/03)
The novel lead bis(1H-2-indolyl)methanone inhibits autophosphorylation of platelet-derived growth factor (PDGF) receptor tyrosine kinase in intact cells. Various substituents in the 5- or 6-position of one indole ring increase or preserve potency, whereas
