914458-26-7 Usage
Uses
Used in Research Applications:
[5-(2-Fluorophenyl)-1-pentyl-1H-pyrrol-3-yl]-1-naphthalenyl-Methanone is used as a research chemical for studying the effects and mechanisms of action of cannabinoids on the human body. It helps scientists understand the interactions between synthetic cannabinoids and the endocannabinoid system, which can contribute to the development of new therapeutic agents and treatments for various conditions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, [5-(2-Fluorophenyl)-1-pentyl-1H-pyrrol-3-yl]-1-naphthalenyl-Methanone may be used as a starting point for the development of new drugs with potential therapeutic applications. Its agonistic effects on cannabinoid receptors could be harnessed to create medications for pain management, anxiety relief, and other conditions where modulation of the endocannabinoid system may be beneficial.
However, it is important to note that due to the potential for abuse and the associated health risks, the use of this chemical in any application must be carefully regulated and monitored to ensure safety and prevent misuse.
Check Digit Verification of cas no
The CAS Registry Mumber 914458-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,4,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 914458-26:
(8*9)+(7*1)+(6*4)+(5*4)+(4*5)+(3*8)+(2*2)+(1*6)=177
177 % 10 = 7
So 914458-26-7 is a valid CAS Registry Number.
914458-26-7Relevant articles and documents
1-Alkyl-2-aryl-4-(1-naphthoyl)pyrroles: New high affinity ligands for the cannabinoid CB1 and CB2 receptors
Huffman, John W.,Padgett, Lea W.,Isherwood, Matthew L.,Wiley, Jenny L.,Martin, Billy R.
, p. 5432 - 5435 (2007/10/03)
Two series of 1-alkyl-2-aryl-4-(1-naphthoyl)pyrroles were synthesized and their affinities for the cannabinoid CB1 and CB2 receptors were determined. In the 2-phenyl series (5) the N-alkyl group was varied from n-propyl to n-heptyl. A second series of 23 1-pentyl-2-aryl-4-(1-naphthoyl)-pyrroles (6) was also prepared. Several compounds in both series have CB1 receptor affinities in the 6-30 nM range. The high affinities of these pyrrole derivatives relative to JWH-030 (1, R = C5H11) support the hypothesis that these pyrroles interact with the CB1 receptor primarily by aromatic stacking.