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Merck
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Key Documents

565770

Sigma-Aldrich

DAPT

≥98% (HPLC), lyophilized, γ-secretase inhibitor, Calbiochem®

别名:

γ-分泌酶抑制剂IIX, DAPT,N-[N-(3,5-二氟苯乙酰基-L-丙氨酰)]-S-苯基甘氨酸-丁酯

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About This Item

经验公式(希尔记法):
C23H26F2N2O4
分子量:
432.46
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.28

product name

γ-分泌酶抑制剂IIX, Gamma-Secretase Inhibitor IX - CAS 208255-80-5, is a cell-permeable inhibitor of γ-secretase (Aβtotal IC₅₀ = 115 nM, Aβ42 IC₅₀ = 200 nM).

品質等級

化驗

≥98% (HPLC)

形狀

lyophilized

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

溶解度

DMSO: 20 mg/mL

運輸包裝

ambient

儲存溫度

−20°C

InChI

1S/C23H26F2N2O4/c1-14(26-19(28)12-15-10-17(24)13-18(25)11-15)21(29)27-20(16-8-6-5-7-9-16)22(30)31-23(2,3)4/h5-11,13-14,20H,12H2,1-4H3,(H,26,28)(H,27,29)/t14-,20-/m0/s1

InChI 密鑰

DWJXYEABWRJFSP-XOBRGWDASA-N

一般說明

一种可渗透细胞的二肽,通过阻断γ-分泌酶来抑制Aβ的产生(AβIC50 = 115 nM,Aβ42 IC50 = 200 nM)。在小鼠N2a细胞和hAPP/hBACE-1转染的人HEK 293细胞中阻止Aβ34生成。据报道,在HEK 293细胞和神经元培养中均具有功能活性,且不影响淀粉-β样前体蛋白(APP)的分泌。在APP转基因小鼠中也显示出显著降低Aβ水平。据报道,可减少3xTgAD 转基因小鼠的细胞外Aβ斑块和细胞内Aβ积累。也可提供25 mM(5 mg/462 µl) γ-分泌酶抑制剂IX(目录号565784)在DMSO中的溶液。
一种细胞渗透性二肽,抑制γ-分泌酶活性并抑制Aβ的产生(Aβ总IC50 = 115 nM;Aβ42 IC50 = 200 nM)。据报道,在过度表达人APP751的HEK293细胞和神经元培养物中都具有功能活性,但是,它不影响淀粉样蛋白b前体蛋白(APP)的分泌。在急性降低APPV717F转基因小鼠的抗体方面有效。在稳定转染瑞典突变体βAPP695的HEK293细胞中,也能有效抑制~6 kDa C-末端裂解产物(CTFg)的产生。据报道,可减少3xTgAD 转基因小鼠的细胞外Aβ斑块和细胞内Aβ积累。

生化/生理作用

产物不与ATP竞争。
可逆:否
细胞可渗透性:是
靶标IC50:115nm抑制Aβ总计产生;200 nM抑制Aβ42的产生

包裝

用惰性气体包装

警告

毒性:标准处理(A)

其他說明

Morohashi, Y., et al. 2006.J. Bio.Chem.Vol.281, 14670.
Nishitomo, K. et al. 2006 J. Neurochem.99, 1555.
Oddo, S., et al. 2004.Neuron43, 321.
Dovey, H.F., et al. 2001.J. Neurochem.76, 173.
Sastre, M., et al. 2001.EMBO Rep.2, 835.
Vandermeeren, M., et al. 2001.Neurosci. Lett.315, 145.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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