n(6)-benzyladenosine has been researched along with n(6)-cyclohexyladenosine in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (25.00) | 18.7374 |
1990's | 2 (25.00) | 18.2507 |
2000's | 3 (37.50) | 29.6817 |
2010's | 1 (12.50) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ijzerman, AP; Soudijn, W; van der Wenden, EM | 1 |
Bey, P; Demeter, DA; Dudley, MW; Lentz, NL; Meng, EC; Ogden, AM; Peet, NP; Weintraub, HJ | 1 |
Bruns, RF; Trivedi, BK | 1 |
Daly, JW | 1 |
Bressi, JC; Buckner, FS; Choe, J; Gelb, MH; Hol, WG; Hough, MT; Van Voorhis, WC; Verlinde, CL | 1 |
Chen, VL; Gao, ZG; Ivanov, AA; Jacobson, KA; Klutz, AM; Wang, B | 1 |
Cappellacci, L; Franchetti, P; Graser, G; Grifantini, M; Jayaram, HN; Lavecchia, A; Petrelli, R; Saiko, P; Szekeres, T; Vita, P | 1 |
Drenichev, MS; Karganova, GG; Kozlovskaya, LI; Kurochkin, NN; Mikhailov, SN; Orlov, AA; Oslovsky, VE; Osolodkin, DI; Palyulin, VA; Solyev, PN | 1 |
1 review(s) available for n(6)-benzyladenosine and n(6)-cyclohexyladenosine
Article | Year |
---|---|
Adenosine receptors: targets for future drugs.
Topics: Adenosine; Adenosine Triphosphate; Animals; Humans; Ligands; Receptors, Cell Surface; Receptors, Purinergic; Structure-Activity Relationship; Xanthines | 1982 |
7 other study(ies) available for n(6)-benzyladenosine and n(6)-cyclohexyladenosine
Article | Year |
---|---|
A steric and electrostatic comparison of three models for the agonist/antagonist binding site on the adenosine A1 receptor.
Topics: Adenosine; Binding Sites; Chemical Phenomena; Chemistry, Physical; Electrochemistry; Models, Molecular; Molecular Conformation; Molecular Structure; Purinergic Antagonists; Receptors, Purinergic; Regression Analysis; Structure-Activity Relationship; Xanthine; Xanthines | 1992 |
A novel synthesis of xanthines: support for a new binding mode for xanthines with respect to adenosine at adenosine receptors.
Topics: Adenosine; Animals; Dogs; Humans; Molecular Conformation; Molecular Structure; Protein Binding; Rats; Receptors, Purinergic; Structure-Activity Relationship; Theophylline; Xanthines | 1990 |
C2,N6-disubstituted adenosines: synthesis and structure-activity relationships.
Topics: Adenosine; Animals; Binding, Competitive; Chemical Phenomena; Chemistry; Rats; Receptors, Purinergic; Structure-Activity Relationship | 1989 |
Adenosine analogues as inhibitors of Trypanosoma brucei phosphoglycerate kinase: elucidation of a novel binding mode for a 2-amino-N(6)-substituted adenosine.
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 |
Probing distal regions of the A2B adenosine receptor by quantitative structure-activity relationship modeling of known and novel agonists.
Topics: Adenosine; Adenosine A2 Receptor Agonists; Binding Sites; Computer Simulation; Drug Design; Humans; Hydrogen Bonding; Hydrophobic and Hydrophilic Interactions; Models, Molecular; Molecular Conformation; Quantitative Structure-Activity Relationship; Receptor, Adenosine A2B; Static Electricity; Stereoisomerism | 2008 |
Ribose-modified purine nucleosides as ribonucleotide reductase inhibitors. Synthesis, antitumor activity, and molecular modeling of N6-substituted 3'-C-methyladenosine derivatives.
Topics: Adenosine; Antineoplastic Agents; Cell Line, Tumor; Enzyme Inhibitors; Humans; Ribonucleotide Reductases; Ribose; Structure-Activity Relationship | 2008 |
New tools in nucleoside toolbox of tick-borne encephalitis virus reproduction inhibitors.
Topics: Animals; Antiviral Agents; Encephalitis Viruses, Tick-Borne; Humans; Molecular Structure; Nucleosides; Structure-Activity Relationship; Virus Internalization; Virus Replication | 2017 |