n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine has been researched along with 3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine in 4 studies
| 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) | 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) |
|---|---|---|---|---|---|
| 214 | 5 | 58 | 8 | 0 | 4 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (75.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jacobson, KA; Ji, XD; Kim, HO; Olah, ME; Siddiqi, SM; Stiles, GL | 1 |
| Fischer, B; Gallo-Rodriguez, C; Ji, XD; Melman, N; Olah, ME; Orlina, J; Pu, Q; Sanders, LH; Siegman, BD; van Galen, PJ | 1 |
| Jacobson, KA; Ji, XD; Li, AH; Melman, N; Moro, S | 1 |
| Campbell, RG; Chen, E; Gao, ZG; Jacobson, KA; Liston, TE; Poe, RB; Salmaso, V; Suresh, RR | 1 |
4 other study(ies) available for n(6)-(3-iodobenzyl)-5'-n-methylcarboxamidoadenosine and 3-iodo-4-aminobenzyl-5'-N-methylcarboxamidoadenosine
| Article | Year |
|---|---|
2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.
Topics: Adenosine; Adenylyl Cyclase Inhibitors; Animals; Brain; Cell Membrane; CHO Cells; Cricetinae; Molecular Structure; Rats; Receptors, Purinergic P1; Recombinant Proteins; Structure-Activity Relationship | 1994 |
Structure-activity relationships of N6-benzyladenosine-5'-uronamides as A3-selective adenosine agonists.
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 |
Structure-activity relationships and molecular modeling of 3, 5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.
Topics: Adenosine; Animals; Binding, Competitive; Brain; Dihydropyridines; Drug Design; Humans; Iodine Radioisotopes; Kinetics; Models, Molecular; Molecular Conformation; Molecular Structure; Purinergic P1 Receptor Antagonists; Pyridines; Radioligand Assay; Rats; Receptor, Adenosine A2A; Receptor, Adenosine A3; Recombinant Proteins; Structure-Activity Relationship | 1998 |
Selective A
Topics: | 2022 |