MK-0752
目录号: PL13305 纯度: ≥98%
CAS No. :471905-41-6
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中文名称
MK-0752
中文别名
MK-0752 抑制剂;顺式-4-[(4-氯苯基)磺酰基]-4-(2,5-二氟苯基)环己烷丙酸;沙利霉素
英文名称
MK-0752
英文别名
MK0752;3-((1r,4s)-4-((4-Chlorophenyl)sulfonyl)-4-(2,5-difluorophenyl)cyclohexyl)propanoic acid;cis-4-[(4-chlorophenyl)sulfonyl]-4-(2,5-difluorophenyl)cyclohexanepropanoic acid;MK-0752;MK-0752 (MK 0752);MK-0752 MK0752;3-((1r,4s)-4-(4-chlorophenylsulfonyl)-4-(2,5-difluorophenyl)cyclohexyl)propanoic acid
Cas No.
471905-41-6
分子式
C21H21O4F2Scl
分子量
442.90
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
MK-0752 是一种高效、口服活性的特异性 γ-分泌酶 (γ-secretase) 抑制剂,对人 SH-SY5Y 细胞 Aβ40 呈剂量依赖性降低,IC50 为 5 nM。MK-0752 穿过血脑屏障。MK-0752 降低体内新生的中枢神经系统 Aβ。
生物活性
MK-0752 is a potent, orally active and specific γ-secretase inhibitor, showing dose-dependent reduction of Aβ40 with an IC 50 of 5 nM in human SH-SY5Y cells. MK-0752 crosses the blood-brain barrier. MK-0752 reduces newly generated CNS Aβ in vivo.
性状
Solid
体内研究(In Vivo)
MK-0752 (60-240 mg/kg; p.o.) decreases the generation of newly produced Aβ in the brain of rhesus monkeys. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male rhesus monkeys
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Cook JJ, et al. Acute gamma-secretase inhibition of nonhuman primate CNS shifts amyloid precursor protein (APP) metabolism from amyloid-beta production to alternative APP fragments without amyloid-beta rebound. J Neurosci. 2010;30(19):6743-6750.
[2]. Krop I, et al. Phase I pharmacologic and pharmacodynamic study of the gamma secretase (Notch) inhibitor MK-0752 in adult patients with advanced solid tumors. J Clin Oncol. 2012;30(19):2307-2313.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (225.78 mM)Ethanol : 10 mg/mL (22.58 mM; Need ultrasonic)
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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