1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine has been researched along with milrinone in 1 studies
Studies (1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine) | Trials (1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine) | Recent Studies (post-2010) (1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine) | Studies (milrinone) | Trials (milrinone) | Recent Studies (post-2010) (milrinone) |
---|---|---|---|---|---|
62 | 0 | 14 | 1,605 | 235 | 452 |
Protein | Taxonomy | 1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine (IC50) | milrinone (IC50) |
---|---|---|---|
Phosphodiesterase | Bos taurus (cattle) | 1 | |
cGMP-dependent 3',5'-cyclic phosphodiesterase | Homo sapiens (human) | 0.3 | |
High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A | Homo sapiens (human) | 0.3 | |
cGMP-specific 3',5'-cyclic phosphodiesterase | Homo sapiens (human) | 0.52 | |
Prostaglandin G/H synthase 1 | Homo sapiens (human) | 4.7 | |
cAMP-specific 3',5'-cyclic phosphodiesterase 4A | Homo sapiens (human) | 6 | |
cAMP-specific 3',5'-cyclic phosphodiesterase 4B | Homo sapiens (human) | 6 | |
cAMP-specific 3',5'-cyclic phosphodiesterase 4C | Homo sapiens (human) | 6 | |
cAMP-specific 3',5'-cyclic phosphodiesterase 4D | Homo sapiens (human) | 3.15 | |
cGMP-inhibited 3',5'-cyclic phosphodiesterase B | Homo sapiens (human) | 1.8674 | |
cGMP-inhibited 3',5'-cyclic phosphodiesterase A | Homo sapiens (human) | 1.8177 | |
cGMP-specific 3',5'-cyclic phosphodiesterase | Bos taurus (cattle) | 5 | |
Phosphodiesterase | Sus scrofa (pig) | 0.843 |
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 1-(1-(2-benzo(b)thienyl)cyclohexyl)piperidine and milrinone
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 |