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標(biāo)簽:GSK-3β Inhibitor II
聯(lián)系人:高小姐
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化學(xué)性質(zhì):
規(guī)格 | 5mg 10mg |
CAS | 478482-75-6 |
別名 | Tip-oxadiazole |
化學(xué)名 | 4-[5-[[(3-iodophenyl)methyl]thio]-1,3,4-oxadiazol-2-yl]-pyridine |
分子式 | C14H10IN3OS |
分子量 | 395.2 |
溶解度 | ≤3mg/ml in DMSO;10mg/ml in dimethyl formamide |
儲存條件 | Store at -20°C |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice |
產(chǎn)品描述:
IC50: 390 nM for GSK-3β
GSK-3β Inhibitor II is a GSK-3β inhibitor.
Glycogen Synthase Kinase-3 (GSK-3), a protein-serine kinase, is implicated in the hormonal control of various regulatory proteins. A number of substrates have been identified, which implicates GSK-3 in the regulation of several physiological processes. Moreover, it has been reported that compounds that specifically inhibit GSK-3 activity may be useful in the treatment of diabetes.
In vitro: In a previous study, by using a virtual screening strategy based on a methodology derived from the CATS molecular descriptor, a novel compound class including GSK-3β Inhibitor II with inhibitory activity against the GSK-3 enzyme was identified via scaffold hopping. GSK-3β Inhibitor II was found to be a potent inhibitor of GSK-3β with the IC50 value of 390 nM. However, GSK-3β Inhibitor II was not able to inhibit another GSK-3 isoform, GSK-3α [1]. Another study found that GSK-3β Inhibitor II could block the functional regulation of p53 through inhibiting GSK-3β, decreasing MDM2 levels, and modulating mitochondrial p53 apoptotic signaling [2].
In vivo: Up to now, there is no animal in vivo data reported.
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原創(chuàng)作者:上海莼試生物技術(shù)有限公司
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賬 戶 名:上海生物
開 戶 行:中國銀行山東省分行營業(yè)部
賬 號:2169 2341 6278