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Roscovitine (Seliciclib,CYC202)

    
99%

Roscovitine (Seliciclib,CYC202)

源葉(MedMol)
S80493 一鍵復制產品信息
186692-46-6
C19H26N6O
354.45
MFCD02266401
6-(芐基氨基)-2(R)-[[1-(羥甲基)丙基]氨基]-9-異丙基嘌呤
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S80493-2mg 99% ¥136.00 2 - - -
S80493-5mg 99% ¥238.00 >10 - - -
S80493-10mg 99% ¥421.60 >10 - - -
S80493-25mg 99% ¥646.00 貨期:2-3天 - - -
S80493-50mg 99% ¥952.00 >10 - - -
S80493-100mg 99% ¥1292.00 貨期:2-3天 - - -
S80493-200mg 99% ¥2244.00 貨期:2-3天 - - -
S80493-250mg 99% ¥2584.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

Seliciclib (Roscovitine) is an orally bioavailable and selective CDKs inhibitor with IC50s of 0.2 μM, 0.65 μM, and 0.7 μM for CDK5, Cdc2, and CDK2, respectively.

產品描述: Seliciclib (Roscovitine) is an orally bioavailable and selective CDKs inhibitor with IC50s of 0.2 μM, 0.65 μM, and 0.7 μM for CDK5, Cdc2, and CDK2, respectively.
靶點: cdc2/cyclin B:0.65 μM (IC50);cdk2/cyclin A:0.7 μM (IC50);Cdk2/cyclin E2:0.7 μM (IC50);CDK5/p35:0.16 μM (IC50);GST-erk1:30 μM (IC50);erk1:34 μM (IC50);erk2:14 μM (IC50);IR tyrosine kinase:70 μM (IC50);CDK
體內研究: Compare with normal controls, Seliciclib (Roscovitine) downregulates phosphorylated ERK1/2 and PPARγ with concomitant increase in E-cadherin, but decrease in Vimentin and Collagen IV. Correspondingly, Seliciclib decreases renal tubulointerstitial fibrosis of diabetic rats. Seliciclib (Roscovitine) is effective in decreasing tubulointerstitial fibrosis via the ERK1/2/PPARγ pathway in diabetic rats. Seliciclib (Roscovitine) (16.5 mg/kg) significantly reduces the rate of tumor growth and increases survival of treated mice. Strikingly, Seliciclib (Roscovitine) treatment leads to complete tumor disappearance in one mouse (25%); moreover, no tumor regrowth in this mouse is found 5 months after completion of the treatment. Mouse weights do not differ significantly between mice treated with Seliciclib and control mice, and behavioral differences between the two groups are also negligible. These results suggest that Seliciclib can be used effectively as a selective tumor growth inhibitor in HPV+ head and neck cancer
參考文獻: 1. Meijer L, et al. Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5. Eur J Biochem. 1997 Jan 15;243(1-2):527-36. 2. Bai X, et al. CDK5 promotes renal tubulointerstitial fibrosis in diabetic nephropathy via erk1/2/pparγ pathway. Oncotarget. 2016 Apr 27. 3. Gary C, et al. Selective antitumor activity of roscovitine in head and neck cancer. Oncotarget. 2016 May 23.
溶解性: DMSO  :  ≥  100  mg/mL  (282.13  mM)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.821 ml 14.106 ml 28.213 ml
5 mM 0.564 ml 2.821 ml 5.643 ml
10 mM 0.282 ml 1.411 ml 2.821 ml
50 mM 0.056 ml 0.282 ml 0.564 ml
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參考文獻

質檢證書(COA)

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摩爾濃度計算器

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