Butyrolactone I

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

Butyrolactone I 是 CDK 和 cdc2 激酶家族的 ATP 竞争性抑制剂。

Butyrolactone I is an ATP-competitive inhibitor of CDK and cdc2 kinase family. Butyrolactone I shows antitumor effects in non-small cell lung, small cell lung, and prostate cancer cell lines.(In Vitro):Butyrolactone I (70 and 100 μM) increases the percentage of DU145 cells in the 4C phase of the cell cycle. Butyrolactone I increases the amount of cyclin B1 positive cells in the 4C phase on day 1 and returns to normal by day 3. Butyrolactone I inhibits Cdc2 of unsynchronized cultured prostate cancer cells and interrupts the cell cycle progression toward cell division. The Butyrolactone I inhibition of Cdc2 led to the accumulation of cells in the 4C phase without mitosis resulting in an accumulation of cyclin B1.

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Olomoucin

Angiogenesis

CDK

Parasite

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87414-49-1

424.44

C24H24O7

>98% (HPLC)

In Vitro:?DMSO : 100 mg/mL (235.60 mM)

C([C@]1(C(OC)=O)C(=C(O)C(=O)O1)C2=CC=C(O)C=C2)C3=CC(CC=C(C)C)=C(O)C=C3

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(-20℃)

With Ice Pack

≥ 2 years