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重要文件

565789

Sigma-Aldrich

γ分泌酶抑制剂 XX

≥95% (HPLC), solid, γ-secretase inhibitor, Calbiochem®

同義詞:

γ分泌酶抑制剂 XX, (S,S)-2-[2-(3,5-二氟苯基)乙酰氨基]-N-(5-甲基-6-氧代-6,7-二氢-5H-二苯并[b,d]氮杂卓-7-基)丙酰胺,DBZ,二苯并氮卓

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About This Item

經驗公式(希爾表示法):
C26H23F2N3O3
CAS號碼:
分子量::
463.48
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77
暫時無法取得訂價和供貨情況

產品名稱

γ分泌酶抑制剂 XX, This γ-secretase inhibitor, CAS 209984-56-5, is a cell-permeable dibenzazepine compound that lowers both brain and plasma Aβ40 levels by ~72% in Tg2576 mutant APP transgenic mouse model.

品質等級

化驗

≥95% (HPLC)

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

white

溶解度

DMSO: 10 mg/mL

運輸包裝

ambient

儲存溫度

−20°C

SMILES 字串

Fc1cc(cc(c1)CC(=O)N[C@@H](C)C(=O)N[C@H]2c3c(cccc3)c4c(cccc4)N(C2=O)C)F

InChI

1S/C26H23F2N3O3/c1-15(29-23(32)13-16-11-17(27)14-18(28)12-16)25(33)30-24-21-9-4-3-7-19(21)20-8-5-6-10-22(20)31(2)26(24)34/h3-12,14-15,24H,13H2,1-2H3,(H,29,32)(H,30,33)/t15-,24-/m0/s1

InChI 密鑰

QSHGISMANBKLQL-OWJWWREXSA-N

一般說明

一种细胞渗透性二苯并氮杂(dbz)化合物,可作为有效的γ-分泌酶抑制剂,在Tg2576突变APP转基因小鼠模型(100 µmol/kg, b.i.d)中,显著降低脑和血浆Aβ40水平,约72%。诱导肠道中隐窝结构增殖单位和结肠干细胞生态位的异质重组。在C57BL/6和ApcMin小鼠模型(10 µmol/kg,i.p.)中,还可能抑制Notch加工(在SupT1细胞中IC50 = 1.7 nM),并诱导增殖隐窝细胞转化为有丝分裂后杯状细胞。
一种细胞渗透性有效γ-分泌酶抑制剂,在Tg2576突变APP转基因小鼠模型(100 µmol/kg,b.i.d.)中可显著降低脑和血浆Aβ40水平,约72%。诱导肠道中隐窝结构增殖单位和结肠干细胞生态位的异质重组。在C57BL/6和ApcMin小鼠模型(10 µmol/kg,i.p.)中,还可能抑制Notch加工(在SupT1细胞中IC50 = 1.7 nM),并诱导增殖隐窝细胞转化为有丝分裂后杯状细胞。

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IC50:1.7 nM抑制SupT1细胞中的Notch加工

包裝

用惰性气体包装

警告

毒性:标准处理(A)

其他說明

Droy-Dupré, L., et al. 2012.Dis.Model Mech.5, 107.
van Es, J.H., et al. 2005.Nature435, 959.
Milano, J., et al. 2004.Toxicol.Sci.82, 341.

法律資訊

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Skin Sens. 1A

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


分析證明 (COA)

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