786701-13-1 Usage
General Description
GW 876008X, also known as 3-(2-Methyl-1-(2-naphthoyl)-1H-indol-3-yl)-N-phenylacrylamide, is a synthetic drug that acts as a potent and selective agonist for the cannabinoid receptor CB2. It has been shown to have anti-inflammatory and analgesic effects in preclinical studies, making it a potential candidate for the treatment of various conditions such as chronic pain, inflammation, and neurodegenerative diseases. GW 876008X has also been investigated for its potential use in cancer therapy, as it has shown promise in inhibiting the growth of cancer cells in vitro. Further research is needed to better understand the full therapeutic potential of this compound and its possible side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 786701-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,6,7,0 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 786701-13:
(8*7)+(7*8)+(6*6)+(5*7)+(4*0)+(3*1)+(2*1)+(1*3)=191
191 % 10 = 1
So 786701-13-1 is a valid CAS Registry Number.
786701-13-1Relevant articles and documents
Identification of a manufacturing route of novel CRF-1 antagonists containing a 2,3-Dihydro-1 H-pyrrolo[2,3-b]pyridine moiety
Ribecai, Arianna,Bacchi, Sergio,Delpogetto, Monica,Guelfi, Simone,Manzo, Angelo Maria,Perboni, Alcide,Stabile, Paolo,Westerduin, Pieter,Hourdin, Marie,Rossi, Sara,Provera, Stefano,Turco, Lucilla
, p. 895 - 901 (2011/03/20)
A case study on the synthesis of novel CRF-1 antagonists containing the 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine moiety is presented. The development of ever more efficient synthetic routes allowed the progression of three candidates at the same time. A manu
PROCESS FOR PREPARING BICYCLIC COMPOUNDS
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, (2008/06/13)
The present invention relates to a process for preparing compounds of formula (IA), which are potent and specific antagonists of corticotropin-releasing factor (CRF) receptors, from intermediate compounds of formula (I), by a coupling reaction catalysed b