产品详情
简单介绍:
PD0325901,MEKInhibitor
详情介绍:
Product Information
Molecular Weight: | 482.19 |
Formula: | C16H14F3IN2O4 |
Purity: | ≥98% |
CAS#: | 391210-10-9 |
Solubility: | DMSO up to 100 mM |
Chemical Name: | N-[(2R)-2,3-Dihydroxypropoxy]-3,4-difluoro-2[(2-fluoro-4-iodophenyl)amino]-benzamide |
Storage: | Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year. |
Biological Activity:
PD0325901 is a highly potent and selective inhibitor of MEK with an IC50 of 0.33 nM. Its potency, selectivity, and solubility are all better than many other MEK inhibitors (e.g., CI-1040). It can potently inhibit the phosphorylation and activation of MAPK/ERK and tumor cell proliferation. In combination with CHIR99021, PD0325901 has been shown to promote mouse ES cell self-renewal and iPSC generation.
How to Use:
- In vitro: PD0325901 was used at 0.01-0.5 µM in vitro and in cellular assays.
- In vivo: PD0325901 was orally administrated to mice at 25 mg/kg once per day.
Reference:
- 1. Barrett SD, et al. The discovery of the benzhydroxamate MEK inhibitors CI-1040 and PD 0325901. (2008) Bioorg. Med. Chem. Lett. 18: 6501-6504.
- 2. Lin T, et al. A chemical platform for improved induction of human iPSCs. (2009) Nature Methods 6, 805-808.
- 3. Henderson YC, et al. MEK inhibitor PD0325901 significantly reduces the growth of papillary thyroid carcinoma cells in vitro and in vivo. (2010) Mol Cancer Ther. 9(7):1968-76.
Products are for research use only. Not for human use. |
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