arg-3-hyp-7-phe-bradykinin has been researched along with sch 23390 in 1 studies
Studies (arg-3-hyp-7-phe-bradykinin) | Trials (arg-3-hyp-7-phe-bradykinin) | Recent Studies (post-2010) (arg-3-hyp-7-phe-bradykinin) | Studies (sch 23390) | Trials (sch 23390) | Recent Studies (post-2010) (sch 23390) |
---|---|---|---|---|---|
52 | 2 | 3 | 803 | 0 | 585 |
Protein | Taxonomy | arg-3-hyp-7-phe-bradykinin (IC50) | sch 23390 (IC50) |
---|---|---|---|
D(2) dopamine receptor | Homo sapiens (human) | 1.0405 | |
D | Rattus norvegicus (Norway rat) | 0.001 | |
D(1A) dopamine receptor | Homo sapiens (human) | 0.0461 | |
D(1B) dopamine receptor | Homo sapiens (human) | 0.0011 | |
D(2) dopamine receptor | Rattus norvegicus (Norway rat) | 0.0006 | |
Sigma non-opioid intracellular receptor 1 | Homo sapiens (human) | 0.3891 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Axe, FU; Bembenek, SD; Butler, CR; Coles, F; Dunford, PJ; Edwards, JP; Fourie, AM; Grice, CA; Karlsson, L; Lundeen, K; Riley, JP; Savall, BM; Tays, KL; Wei, J; Williams, KN; Xue, X | 1 |
1 other study(ies) available for arg-3-hyp-7-phe-bradykinin and sch 23390
Article | Year |
---|---|
Identification of a potent, selective, and orally active leukotriene a4 hydrolase inhibitor with anti-inflammatory activity.
Topics: Administration, Oral; Animals; Anti-Inflammatory Agents; Catalysis; Dogs; Drug Evaluation, Preclinical; Enzyme Inhibitors; Epoxide Hydrolases; Humans; Magnetic Resonance Spectroscopy; Mice; Structure-Activity Relationship | 2008 |