產(chǎn)品描述: | Flavopiridol Hydrochloride (Alvocidib Hydrochloride) is a broad inhibitor of CDK, competing with ATP to inhibit CDKs including CDK1, CDK2, CDK4 with IC50s of 30, 170, 100 nM, respectively. |
靶點(diǎn): |
CDK1/Cyc B1:30 nM (IC50);CDK2/Cyc E:170 nM (IC50);CDK4/Cyc D1:100 nM (IC50);MAP:19000 nM (IC50);PKC:14000 nM (IC50);EGFR:22000 nM (IC50);HIVProtease;CDK;Autophagy |
參考文獻(xiàn): |
1. Mahoney E, et al. ER stress and autophagy: new discoveries in the mechanism of action and drug resistance of the cyclin-dependent kinase inhibitor flavopiridol.Blood. 2012 Aug 9;120(6):1262-1273. 2. Keskin H, et al. Complex effects of flavopiridol on the expression of primary response genes. Cell Div. 2012 Mar 29;7:11. 3. Kim KS, et al.Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: synthesis and biological effects. J Med Chem. 2000 Nov 2;43(22):4126-34. |
溶解性: |
DMSO : ≥ 20 mg/mL (45.63 mM) H2O : ≥ 20 mg/mL (45.63 mM) DMF : 7.69 mg/mL (17.55 mM; Need ultrasonic) |
保存條件: |
-20℃ |
配置溶液濃度參考: |
|
1mg |
5mg |
10mg |
1 mM |
2.282 ml |
11.408 ml |
22.815 ml |
5 mM |
0.456 ml |
2.282 ml |
4.563 ml |
10 mM |
0.228 ml |
1.141 ml |
2.282 ml |
50 mM |
0.046 ml |
0.228 ml |
0.456 ml |
|
注意: |
部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。 |