Stemolecule™ PD0325901
1. Bain, J. et al., Biochem. J. 408:297-315 (2007).
2. Sebolt-Leopold, J. S. ∓ Herrera, R. Nature Rev. Cancer 4:937-947 (2004).
Stemolecule™ PD0325901
PD0325901 is an orally bioavailable, synthetic organic molecule targeting mitogen-activated protein kinase kinase (MAPK/ERK kinase or MEK) with potential antineoplastic activity. PD0325901, a derivative of MEK inhibitor CI-1040, selectively binds to and inhibits MEK, which may result in the inhibition of the phosphorylation and activation of MAPK/ERK and the inhibition of tumor cell proliferation1,2.
References
- Bain, J. et al., Biochem. J. 408:297-315 (2007).
- Sebolt-Leopold, J. S. ∓ Herrera, R. Nature Rev. Cancer 4:937-947 (2004).
- Tongxiang Lin, Rajesh Ambasudhan, Xu Yuan, Wenlin Li, Simon Hilcove, Ramzey Abujarour, Xiangyi Lin, Heung Sik Hahm, Ergeng Hao, Alberto Hayek & Sheng Ding. (2009) A chemical platform for improved induction of human iPSCs. Nat Meth 1393.
For research use only. Not for use in diagnostic procedures. Not for resale.
Stemolecule™ PD0325901
| Chemical Formula | C16H14F3IN2O4 |
| Structure |
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| Molecular Weight | 482.19 |
| Purity | >98% by HPLC analysis |
| Formulation | Pale purple solid |
| Solubility | Soluble in DMSO (100 mM). For a 10 mM concentrated stock solution, reconstitute the compound by adding 415 µl of DMSO to the entire contents of the vial. Note: for most cells, the maximum tolerance to DMSO is <0.5%. |
| Storage | 4°C protected from light. Following reconstitution, store aliquots at -20°C |
| Stability | Stock solutions stable at -20°C for 6 months |
| Quality Control | The purity of PD0325901 was determined by HPLC analysis. The accurate mass and structure of PD0325901 was determined by mass spectrometry and NMR, respectively. Cellular toxicity of PD0325901 was tested by using HeLa and HEK293 cells. |
| References |
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