About 9 results found for searched term "66-97-7" (0.059 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M4478 | Psoralen | DNA/RNA Synthesis |
| Ficusin; Furocoumarin | ||
| Psoralen(Furocoumarin) is an active ingredient from Fructus Psoraleae; has anticancer activity. | ||
| M6518 | BMS 453 | Others |
| BMS 453 is a synthetic retinoid and RARβ agonist; also RARα and RARγ antagonist. | ||
| M7070 | O-1918 | Others |
| O-1918 is a silent antagonist for putative abnormal-CBD receptor. | ||
| M28766 | Tavapadon | Dopamine Receptor |
| PF-06649751; CVL-751 | ||
| Tavapadon (PF-06649751) is a potentially best-in-class, orally active, highly selective dopamine D1/D5 receptor partial agonist for studies related to Parkinson's disease (PD). | ||
| M30457 | VQW-765 | AChR/AChE |
| AQW-051 | ||
| VQW-765 (AQW-051) is a selective and orally active alpha-7 nicotinic acetylcholine receptor (α7-nAChR) agonist with a pKD value of 7.56 to recombinantly expressed human α7-nAChR. VQW-765 shows anxiolytic-like effect in vivo. VQW-765 can be used for the research of anxiety disorder and acute performance anxiety. | ||
| M41930 | PAT-IN-1 | Ras |
| PAT-IN-1 is a protein acyl transferases (PAT) inhibitor. | ||
| M42622 | URAT1&XO inhibitor 1 | Xanthine Oxidase |
| URAT1&XO inhibitor 1 is a dual inhibitor of both URAT1 (IC50=~10 μM) and Xanthine Oxidase (IC50=1.01 μM). | ||
| M49769 | ZDWX-25 | GSK-3 |
| ZDWX-25 is a highly potent GSK-3β and DYRK1A dual inhibitor with an IC50 value of 71 nM for GSK-3β. | ||
| M50431 | Phospho-Glycogen Synthase Peptide-2(substrate) | GSK-3 |
| Phospho-Glycogen Synthase Peptide-2 (substrate) is peptide substrate for glycogen synthase kinase-3 (GSK-3) and can be used for affinity purification of protein-serine kinases. | ||
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