Compounds > 2-chloro-n(6)cyclopentyladenosine
Page last updated: 2024-09-03

2-chloro-n(6)cyclopentyladenosine and 3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine

2-chloro-n(6)cyclopentyladenosine has been researched along with 3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine in 1 studies

Compound Research Comparison

Studies
(2-chloro-n(6)cyclopentyladenosine)		Trials
(2-chloro-n(6)cyclopentyladenosine)		Recent Studies (post-2010)
(2-chloro-n(6)cyclopentyladenosine)		Studies
(3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine)		Trials
(3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine)		Recent Studies (post-2010) (3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine)
252043804

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jacobson, KA; Ji, XD; Kim, HO; Olah, ME; Siddiqi, SM; Stiles, GL1

Other Studies

1 other study(ies) available for 2-chloro-n(6)cyclopentyladenosine and 3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine

ArticleYear
2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.
    Journal of medicinal chemistry, 1994, Oct-14, Volume: 37, Issue:21

    Topics: Adenosine; Adenylyl Cyclase Inhibitors; Animals; Brain; Cell Membrane; CHO Cells; Cricetinae; Molecular Structure; Rats; Receptors, Purinergic P1; Recombinant Proteins; Structure-Activity Relationship

1994