7-bromoeudistomine d has been researched along with adenosine-5'-(n-ethylcarboxamide) in 2 studies
Studies (7-bromoeudistomine d) | Trials (7-bromoeudistomine d) | Recent Studies (post-2010) (7-bromoeudistomine d) | Studies (adenosine-5'-(n-ethylcarboxamide)) | Trials (adenosine-5'-(n-ethylcarboxamide)) | Recent Studies (post-2010) (adenosine-5'-(n-ethylcarboxamide)) |
---|---|---|---|---|---|
6 | 0 | 0 | 1,333 | 4 | 133 |
Protein | Taxonomy | 7-bromoeudistomine d (IC50) | adenosine-5'-(n-ethylcarboxamide) (IC50) |
---|---|---|---|
Adenosine receptor A3 | Homo sapiens (human) | 0.0097 | |
Alpha-2B adrenergic receptor | Rattus norvegicus (Norway rat) | 0.037 | |
Alpha-2C adrenergic receptor | Rattus norvegicus (Norway rat) | 0.037 | |
Alpha-2A adrenergic receptor | Rattus norvegicus (Norway rat) | 0.037 | |
Adenosine receptor A1 | Rattus norvegicus (Norway rat) | 0.4498 | |
Adenosine receptor A2a | Homo sapiens (human) | 0.0336 | |
Adenosine receptor A2b | Rattus norvegicus (Norway rat) | 0.0175 | |
Adenosine receptor A1 | Homo sapiens (human) | 0.0007 | |
Adenosine receptor A2a | Rattus norvegicus (Norway rat) | 0.0513 | |
Adenosine receptor A1 | Gallus gallus (chicken) | 0.017 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ishiyama, H; Kobayashi, J; Nakata, H; Ohshita, K; Oyanagi, K | 1 |
Abe, T; Ishiyama, H; Kobayashi, J; Nakata, H; Ohshita, K | 1 |
2 other study(ies) available for 7-bromoeudistomine d and adenosine-5'-(n-ethylcarboxamide)
Article | Year |
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Synthesis of hybrid molecules of caffeine and eudistomin D and its effects on adenosine receptors.
Topics: Binding Sites; Caffeine; Carbolines; Cell Line; Humans; Ligands; Molecular Structure; Receptors, Purinergic P1; Structure-Activity Relationship | 2007 |
Synthesis of eudistomin D analogues and its effects on adenosine receptors.
Topics: Carbolines; Cell Line; Humans; Molecular Structure; Receptors, Purinergic P1; Structure-Activity Relationship | 2008 |