About 6 results found for searched term "87-52-5" (0.055 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1765 | Crizotinib (PF-02341066) | c-Met |
| Crizotinib | ||
| Crizotinib (PF-02341066) is a potent, orally bioavailable, ATP-competitive small-molecule inhibitor of c-Met kinase and ALK (anaplastic lymphoma kinase) with IC50 values to be 4 and 25 nM for C-Met and ALK resepectively. | ||
| M7630 | Butein | PDE |
| 2’,3,4,4’-tetrahydroxy Chalcone | ||
| Butein is a cAMP-specific PDE inhibitor with an IC50 of 10.4 μM for PDE4. Butein is a specific protein tyrosine kinase inhibitor with IC50s of 16 and 65 μM for EGFR and p60c-src in HepG2 cells. Butein sensitizes HeLa cells to Cisplatin through AKT and ERK/p38 MAPK pathways by targeting FoxO3a. Butein is a SIRT1 activator. | ||
| M8494 | BMS 204352 | Others |
| BMS 204352 is a potassium channel modulator. | ||
| M13887 | Gramine | Adrenergic Receptor |
| Donaxine | ||
| Gramine (Donaxine) is a natural alkaloid isolated from giant reed, acts as an active adiponectin receptor (AdipoR) agonist, with IC50s of 3.2 and 4.2 µM for AdipoR2 and AdipoR1, respectively. | ||
| M30783 | YIL781 | Ghrelin Receptor/GHSR |
| YIL781 is a potent and orally active ghrelin receptor (GHSR) antagonist. YIL781 produces a greater improvement in glucose homeostasis in rats. YIL-781 hydrochloride inhibits the calcium response induced by ghrelin with pIC50 values of 7.90 and 8.27, respectively. | ||
| M40630 | NF-κΒ activator 1 | NF-κB |
| NF-κΒ activator 1 is a potent NF-κΒ activator with an EC50 of 0.9 μM and induces superoxide dismutase (SOD)2 mRNA expression. | ||
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