跳转至内容
Merck
所有图片(1)

Key Documents

344930

Sigma-Aldrich

弗林蛋白酶抑制剂I

≥90% (HPLC), solid, furin inhibitor, Calbiochem®

别名:

弗林蛋白酶抑制剂I

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C34H66ClN11O5
分子量:
744.41
分類程式碼代碼:
12352200
NACRES:
NA.28

product name

弗林蛋白酶抑制剂I, Furin Inhibitor I, is a peptidyl chloromethylketone that binds to the catalytic site of furin and blocks its activity.

品質等級

化驗

≥90% (HPLC)

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
desiccated

顏色

off-white

溶解度

methanol: 1 mg/mL
DMSO: soluble

運輸包裝

ambient

儲存溫度

−20°C

一般說明

一种不可逆结合弗林蛋白酶催化位点并阻断其活性的肽基氯甲基酮。因此,它可以用作病毒糖蛋白的高度特异性裂解抑制剂和病毒复制的阻滞剂。据报道,弗林蛋白酶可以阻断MT5-MMP的脱落并阻止MT5-MMP的活化。完全抑制纯化的弗林蛋白酶或PACE4对Boc-RVRR-AMC(50 µM)的裂解。也抑制内皮素转化酶的活性,减少BACE(β-位点APP裂解酶)的前肽裂解。
一种结合弗林蛋白酶催化位点并阻断其活性的肽基氯甲基酮。因此,它可以用作病毒糖蛋白的高度特异性裂解抑制剂和病毒复制的阻滞剂。据报道,弗林蛋白酶可以阻断MT5-MMP的脱落并阻止MT5-MMP的活化。还显示可减少BACE(β-位点APP裂解酶)的前肽裂解。

生化/生理作用

主要靶标
病毒糖蛋白
产物不与ATP竞争。
可逆:否
细胞可渗透性:是

警告

毒性:标准处理(A)

序列

癸酰基-Arg-Val-Lys-Arg-CMK

外觀

作为三氟乙酸盐提供。

重構

复溶后,等分并冷冻(-20°C)。储备液可在-20°C最长稳定1个月。

其他說明

Sugrue, R.J., et al. 2001.J. Gen.Virol.82, 1375.
Wang, X., and Pei, D. 2001.J. Biol. Chem.276, 35953.
Capell, A., et al. 2000.J. Biol. Chem. 275, 30849.
Denault, J.B., et al. 1995.FEBS Lett.362, 276.
Denault, J.B., et al. 1995.J. Cardiovasc.Pharmacol.26, S47.
Garten, W., et al. 1994.Biochimie 76, 217.
Hallenberger, S., et al. 1992.Nature 360, 358.
Stieneke-Gröber, A., et al. 1992.EMBO J. 11, 2407.

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


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Lijuan Du et al.
Nature communications, 13(1), 3482-3482 (2022-06-18)
How signaling proteins generate a multitude of information to organize tissue patterns is critical to understanding morphogenesis. In Drosophila, FGF produced in wing-disc cells regulates the development of the disc-associated air-sac-primordium (ASP). Here, we show that FGF is Glycosylphosphatidylinositol-anchored to
Carlota Oleaga et al.
Journal of lipid research, 62, 100003-100003 (2021-01-12)
Proprotein convertase subtilisin/kexin type 9 (PCSK9) regulates cholesterol metabolism by inducing the degradation of hepatic low density lipoprotein receptors (LDLRs). Plasma PCSK9 has 2 main molecular forms: a 62 kDa mature form (PCSK9_62) and a 55 kDa, furin-cleaved form (PCSK9_55).
Fangyuan Chen et al.
Molecular systems biology, 17(8), e10239-e10239 (2021-08-03)
Understanding the mechanism of SARS-CoV-2 infection and identifying potential therapeutics are global imperatives. Using a quantitative systems pharmacology approach, we identified a set of repurposable and investigational drugs as potential therapeutics against COVID-19. These were deduced from the gene expression
Zhujun Ao et al.
iScience, 25(8), 104759-104759 (2022-07-21)
The Delta variant had spread globally in 2021 and caused more serious disease than the original virus and Omicron variant. In this study, we investigated several virological features of Delta spike protein (SPDelta), including protein maturation, its impact on viral
Montalbano Mauro et al.
International journal of molecular sciences, 24(13) (2023-07-14)
Glypican-3 (GPC-3) is a heparin sulfate proteoglycan located extracellularly and anchored to the cell membrane of transformed hepatocytes. GPC-3 is not expressed in normal or cirrhotic liver tissue but is overexpressed in hepatocellular carcinoma (HCC). Because of this, GPC-3 is

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门