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n-cyclopropyl adenosine-5'-carboxamide and n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine

n-cyclopropyl adenosine-5'-carboxamide has been researched along with n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine in 2 studies

Compound Research Comparison

Studies
(n-cyclopropyl adenosine-5'-carboxamide)
Trials
(n-cyclopropyl adenosine-5'-carboxamide)
Recent Studies (post-2010)
(n-cyclopropyl adenosine-5'-carboxamide)
Studies
(n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine)
Trials
(n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine)
Recent Studies (post-2010) (n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine)
1405214558

Protein Interaction Comparison

ProteinTaxonomyn-cyclopropyl adenosine-5'-carboxamide (IC50)n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine (IC50)
high affinity choline transporter 1 isoform aHomo sapiens (human)2.1002
Adenosine receptor A3Homo sapiens (human)0.0017

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
Fischer, B; Gallo-Rodriguez, C; Ji, XD; Melman, N; Olah, ME; Orlina, J; Pu, Q; Sanders, LH; Siegman, BD; van Galen, PJ1
de Zwart, M; IJzerman, AP; Kooijman, H; Kourounakis, A; Link, R; Spek, AL; von Frijtag Drabbe Künzel, JK1

Other Studies

2 other study(ies) available for n-cyclopropyl adenosine-5'-carboxamide and n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine

ArticleYear
Structure-activity relationships of N6-benzyladenosine-5'-uronamides as A3-selective adenosine agonists.
    Journal of medicinal chemistry, 1994, Mar-04, Volume: 37, Issue:5

    Topics: Adenosine; Adenosine-5'-(N-ethylcarboxamide); Animals; Brain; Cell Membrane; Cerebral Cortex; CHO Cells; Cricetinae; Molecular Structure; Rats; Receptors, Purinergic P1; Structure-Activity Relationship

1994
5'-N-substituted carboxamidoadenosines as agonists for adenosine receptors.
    Journal of medicinal chemistry, 1999, Apr-22, Volume: 42, Issue:8

    Topics: Adenosine; Animals; Cell Line; Cerebral Cortex; CHO Cells; Corpus Striatum; Cricetinae; Crystallography, X-Ray; Cyclic AMP; Humans; In Vitro Techniques; Molecular Conformation; Purinergic P1 Receptor Agonists; Radioligand Assay; Rats; Receptors, Purinergic P1; Structure-Activity Relationship

1999