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Flavopiridol HCl

    
96%

Flavopiridol Hydrochloride

源葉(MedMol)
S80274 一鍵復(fù)制產(chǎn)品信息
131740-09-5
C21H21Cl2NO5
438.3
HMR-1275, L86-8275;2-(2-chlorophenyl)-5,7-dihydroxy-8-((3S,4R)-3-hydroxy-1-methylpiperidin-4-yl)-4H-chromen-4-one hydrochloride
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S80274-2mg 96% ¥255.00 5 - - -
S80274-5mg 96% ¥357.00 5 - - -
S80274-10mg 96% ¥540.00 5 - - -
S80274-25mg 96% ¥1105.00 6 - - -
S80274-50mg 96% ¥1890.00 貨期:2-3天 - - -
S80274-100mg 96% ¥3060.00 貨期:2-3天 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

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.

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: 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: 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
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參考文獻

質(zhì)檢證書(COA)

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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

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