United States (Change Country)Roscovitine (Seliciclib, CYC202) Chemical Structure
Roscovitine (Seliciclib, CYC202) is a potent and selective inhibitor of cyclin-dependent kinases (cdks). This agent displays higher inhibitory potency and higher selectivity compared to olomoucine. [1]
Roscovitine (Seliciclib, CYC202) inhibits p34 cdc2/cyclin B (IC50 = 0.65 µM), p33 cdk2/cyclin A(IC50 = 0.70 µM), p33 cdk2/cyclin E (IC50 = 0.70 µM), and p33 cdk2/p35(IC50 = 0.20 µM) by competing for the ATP binding domain of these kinases. Roscovitine (Seliciclib, CYC202) exhibits very low sensitivity towards related kinases, such as erk1 and erk2 (IC50 = 34 µM and 14 µM, respectively) .[2]
Roscovitine (Seliciclib, CYC202) doesnot significantly affect the activity of other protein kinases even at 100 µM and compared to olomoucine. Roscovitine displays increased anti-mitotic activity at the G1/S and G2/M phases of the cell cycle. [3]
[3] Anticancer Res. 1998 Mar-Apr;18(2A):751-5.
[1] Eur. J. Biochem 1997;243:518-526
[2] The Plant Journal 1997;12(1), 191-202
| Molecular Weight (WM): | 354.45 |
|---|---|
| Formula: | C19H26N6O |
| Solubility(R.T.:25°C): | DMSO 71mg/mL |
| Water <1mg/mL | |
| Ethanol 6mg/mL |
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Data from [PNAS 2011;108, 8417] Roscovitine (Seliciclib, CYC202) purchased from Selleck
;Bai Bo University of Hong Kong Roscovitine (Seliciclib, CYC202) purchased from Selleck
;The Journal of Neuroscience, 2012, 32(32):11050-11066 Roscovitine (Seliciclib, CYC202) purchased from Selleck
Data from [PNAS 2011;108, 8417] Roscovitine (Seliciclib, CYC202) purchased from Selleck
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