205171-06-8 Usage
General Description
N-Cyclopentyl-2'-C-methyl-adenosine is a chemical compound that is a modified form of adenosine, a naturally occurring nucleoside. N-Cyclopentyl-2'-C-methyl-adenosine contains a cyclopentyl group and a 2'-C-methyl substitution on the adenosine molecule. It has been studied for its potential medicinal properties, particularly as a potential therapeutic agent for the treatment of various diseases and conditions. N-Cyclopentyl-2'-C-methyl-adenosine has been investigated for its potential effects on the cardiovascular system, as well as its potential as an anti-inflammatory and immunosuppressive agent. Research has also explored its potential as a modulator of adenosine receptor activity, which could have implications for the treatment of certain neurological disorders. Overall, N-Cyclopentyl-2'-C-methyl-adenosine is a compound of interest in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 205171-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,1,7 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 205171-06:
(8*2)+(7*0)+(6*5)+(5*1)+(4*7)+(3*1)+(2*0)+(1*6)=88
88 % 10 = 8
So 205171-06-8 is a valid CAS Registry Number.
205171-06-8Relevant articles and documents
N6-cycloalkyl- And n6-bicycloalkyl-c5'(c 2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice
Franchetti, Palmarisa,Cappellacci, Loredana,Vita, Patrizia,Petrelli, Riccardo,Lavecchia, Antonio,Kachler, Sonja,Klotz,Marabese, Ida,Luongo, Livio,Maione, Sabatino,Grifantini, Mario
scheme or table, p. 2393 - 2406 (2010/04/30)
To further investigate new potent and selective human A1 adenosine receptor agonists, we have synthesized a series of 5'-chloro-5'-deoxy- and 5'-(2-fluorophenylthio)-5'-deoxy-N6-cycloalkyl(bicycloalkyl)- substituted adenosine and 2'-C-methylade
2'-C-Methyl analogues of selective adenosine receptor agonists: Synthesis and binding studies
Franchetti, Palmarisa,Cappellacci, Loredana,Marchetti, Stefano,Trincavelli, Letizia,Martini, Claudia,Mazzoni, Maria R.,Lucacchini, Antonio,Grifantini, Mario
, p. 1708 - 1715 (2007/10/03)
2'-C-Methyl analogues of selective adenosine receptor agonists such as (R)-PIA, CPA, CCPA, NECA, and IB-MECA were synthesized in order to further investigate the subdomain that binds the ribose moiety. Binding affinities of these new compounds at A1
