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8-(dicyclopropylmethyl)-1,3-dipropylxanthine and n(6)-cyclopentyladenosine

8-(dicyclopropylmethyl)-1,3-dipropylxanthine has been researched along with n(6)-cyclopentyladenosine in 2 studies

Compound Research Comparison

Studies
(8-(dicyclopropylmethyl)-1,3-dipropylxanthine)
Trials
(8-(dicyclopropylmethyl)-1,3-dipropylxanthine)
Recent Studies (post-2010)
(8-(dicyclopropylmethyl)-1,3-dipropylxanthine)
Studies
(n(6)-cyclopentyladenosine)
Trials
(n(6)-cyclopentyladenosine)
Recent Studies (post-2010) (n(6)-cyclopentyladenosine)
1400605062

Protein Interaction Comparison

ProteinTaxonomy8-(dicyclopropylmethyl)-1,3-dipropylxanthine (IC50)n(6)-cyclopentyladenosine (IC50)
Adenosine receptor A1Rattus norvegicus (Norway rat)0.2256
Adenosine receptor A2bRattus norvegicus (Norway rat)1.16
Adenosine receptor A1Homo sapiens (human)0.0027
Adenosine receptor A2aRattus norvegicus (Norway rat)1.16

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ishii, A; Nonaka, H; Shimada, J; Suzuki, F1
Jacobson, KA; van Galen, PJ; Williams, M1

Reviews

1 review(s) available for 8-(dicyclopropylmethyl)-1,3-dipropylxanthine and n(6)-cyclopentyladenosine

ArticleYear
Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential.
    Journal of medicinal chemistry, 1992, Feb-07, Volume: 35, Issue:3

    Topics: Adenosine; Animals; Humans; Models, Chemical; Receptors, Purinergic; Second Messenger Systems; Structure-Activity Relationship

1992

Other Studies

1 other study(ies) available for 8-(dicyclopropylmethyl)-1,3-dipropylxanthine and n(6)-cyclopentyladenosine

ArticleYear
8-Polycycloalkyl-1,3-dipropylxanthines as potent and selective antagonists for A1-adenosine receptors.
    Journal of medicinal chemistry, 1992, Mar-06, Volume: 35, Issue:5

    Topics: Adenosine; Adenosine-5'-(N-ethylcarboxamide); Animals; Binding, Competitive; Cell Membrane; Corpus Striatum; Guinea Pigs; Humans; Molecular Conformation; Molecular Structure; Prosencephalon; Purinergic Antagonists; Rats; Receptors, Purinergic; Stereoisomerism; Structure-Activity Relationship; Xanthines

1992