n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine has been researched along with dinoprost in 1 studies
Studies (n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine) | Trials (n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine) | Recent Studies (post-2010) (n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine) | Studies (dinoprost) | Trials (dinoprost) | Recent Studies (post-2010) (dinoprost) |
---|---|---|---|---|---|
79 | 1 | 16 | 11,554 | 940 | 1,936 |
Protein | Taxonomy | n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine (IC50) | dinoprost (IC50) |
---|---|---|---|
Prostaglandin G/H synthase 1 | Bos taurus (cattle) | 0.0025 | |
Prostaglandin G/H synthase 2 | Bos taurus (cattle) | 0.0713 | |
Prostaglandin G/H synthase 1 | Homo sapiens (human) | 0.14 | |
Prostaglandin E2 receptor EP1 subtype | Homo sapiens (human) | 0.3 | |
Prostaglandin G/H synthase 2 | Homo sapiens (human) | 0.14 | |
Prostaglandin E2 receptor EP4 subtype | Homo sapiens (human) | 4.2 | |
Prostaglandin F2-alpha receptor | Bos taurus (cattle) | 0.14 | |
Prostaglandin F2-alpha receptor | Homo sapiens (human) | 0.0139 | |
Prostaglandin E2 receptor EP3 subtype | Homo sapiens (human) | 0.216 | |
Prostaglandin D2 receptor | Homo sapiens (human) | 4.5 | |
Solute carrier organic anion transporter family member 2B1 | Rattus norvegicus (Norway rat) | 0.287 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P | 1 |
1 other study(ies) available for n-(n-(3-carboxyoxirane-2-carbonyl)leucyl)isoamylamine and dinoprost
Article | Year |
---|---|
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship | 2012 |