Compounds > n(6)-benzyladenosine
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n(6)-benzyladenosine and metrifudil

n(6)-benzyladenosine has been researched along with metrifudil in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Daly, DT; Kusachi, S; Olsson, RA; Thompson, RD; Yamada, N1
Cristalli, G; Esker, JL; Jacobson, KA; Ji, XD; Melman, N; Olah, ME; Schneller, SW; Secrist, JA; Siddiqi, SM; Tiwari, KN1
Aronov, AM; Gelb, MH; Hol, WG; Verlinde, CL1
Bressi, JC; Buckner, FS; Choe, J; Gelb, MH; Hol, WG; Hough, MT; Van Voorhis, WC; Verlinde, CL1
Chakrabarty, K; Dolezal, K; Hauserová, E; Holub, J; Krystof, V; Novák, O; Popa, I; Spíchal, L; Strnad, M; Voller, J1
Arita, M; Shimizu, H; Wakita, T1

Other Studies

6 other study(ies) available for n(6)-benzyladenosine and metrifudil

ArticleYear
Dog coronary artery adenosine receptor: structure of the N6-aryl subregion.
    Journal of medicinal chemistry, 1986, Volume: 29, Issue:6

    Topics: Adenosine; Animals; Coronary Vessels; Dogs; Models, Structural; Protein Binding; Receptors, Cell Surface; Receptors, Purinergic; Serum Albumin; Structure-Activity Relationship

1986
Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors.
    Journal of medicinal chemistry, 1995, Mar-31, Volume: 38, Issue:7

    Topics: Adenosine; Animals; Cell Membrane; CHO Cells; Corpus Striatum; Cricetinae; In Vitro Techniques; Magnetic Resonance Spectroscopy; Purinergic P1 Receptor Agonists; Purinergic P1 Receptor Antagonists; Purines; Radioligand Assay; Rats; Recombinant Proteins; Ribose; Structure-Activity Relationship

1995
Selective tight binding inhibitors of trypanosomal glyceraldehyde-3-phosphate dehydrogenase via structure-based drug design.
    Journal of medicinal chemistry, 1998, Nov-19, Volume: 41, Issue:24

    Topics: Adenosine; Animals; Binding Sites; Crystallography, X-Ray; Drug Design; Enzyme Inhibitors; Glyceraldehyde-3-Phosphate Dehydrogenases; Humans; Leishmania mexicana; Models, Molecular; NAD; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei brucei

1998
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: elucidation of a novel binding mode for a 2-amino-N(6)-substituted adenosine.
    Journal of medicinal chemistry, 2000, Nov-02, Volume: 43, Issue:22

    Topics: Adenosine; Animals; Combinatorial Chemistry Techniques; Crystallography, X-Ray; Enzyme Inhibitors; Glyceraldehyde-3-Phosphate Dehydrogenases; Glycerolphosphate Dehydrogenase; Models, Molecular; Molecular Conformation; Phosphoglycerate Kinase; Protein Binding; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma brucei brucei; Trypanosoma cruzi

2000
Preparation, biological activity and endogenous occurrence of N6-benzyladenosines.
    Bioorganic & medicinal chemistry, 2007, Jun-01, Volume: 15, Issue:11

    Topics: Adenosine; Animals; Antineoplastic Agents; Arabidopsis Proteins; Biological Assay; Cells, Cultured; Cytokinins; Fibroblasts; Histidine Kinase; Mice; NIH 3T3 Cells; Plant Cells; Plants; Protein Kinases; Receptors, Cell Surface

2007
Characterization of pharmacologically active compounds that inhibit poliovirus and enterovirus 71 infectivity.
    The Journal of general virology, 2008, Volume: 89, Issue:Pt 10

    Topics: Adenosine; Animals; Antiviral Agents; Benzenesulfonates; Capsid Proteins; Cell Line; Drug Resistance, Viral; Enterovirus; Humans; Indoles; Luciferases; Mice; Microbial Sensitivity Tests; Mutation; Phenols; Poliovirus; Replicon; RNA Interference; Virus Replication

2008