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AEBSF HCl {[allProObj[0].p_purity_real_show]}

货号:A395798 同义名: AEBSF盐酸盐 / AEBSF (hydrochloride); AEBSF HCl

AEBSF hydrochloride是一种不可逆的蛋白酶抑制剂,作用于诸如胰凝乳蛋白酶、卡利克雷因、纤溶酶、凝血酶和胰蛋白酶等蛋白酶。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
AEBSF HCl 化学结构 CAS号:30827-99-7
AEBSF HCl 化学结构
CAS号:30827-99-7
AEBSF HCl 3D分子结构
CAS号:30827-99-7
AEBSF HCl 化学结构 CAS号:30827-99-7
AEBSF HCl 3D分子结构 CAS号:30827-99-7
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AEBSF HCl 纯度/质量文件 产品仅供科研

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AEBSF HCl 生物活性

描述 AEBSF directly inhibits β-secretase, thereby suppressing the constant production of Aβ across five diverse human cell lines, including both neural and non-neural types[1]. As a serine protease inhibitor, AEBSF prevents the lysis of leukemic cells by human macrophages without affecting the macrophage release of TNF-α and IL-1β[2]. AEBSF disrupts blastocyst development on endometrial cells and impedes the adhesion of HeLa cells to HUVECs by modifying the pattern of protein secretion[4].
体内研究

AEBSF administration (76.8 mg/kg daily, i.p.) extends the survival time of mice infected with a lethal T. gondii [3].

AEBSF also mitigates airway responsiveness and associated inflammation in a mouse model induced by cockroach allergens[4].

体外研究

AEBSF directly inhibits β-secretase, thereby suppressing the constant production of Aβ across five diverse human cell lines, including both neural and non-neural types[1].

As a serine protease inhibitor, AEBSF prevents the lysis of leukemic cells by human macrophages without affecting the macrophage release of TNF-α and IL-1β[2].

AEBSF disrupts blastocyst development on endometrial cells and impedes the adhesion of HeLa cells to HUVECs by modifying the pattern of protein secretion[4].

AEBSF HCl 细胞实验

Cell Line
Concentration Treated Time Description References
Neutrophils 1 mM 1 hour Inhibition of IL-1β secretion Front Immunol. 2018 Feb 19;9:269.
Human umbilical vein endothelial cells (HUVEC) 1 mg/ml 1 hour Evaluate the uptake of PG-AF in HUVEC, showing that PG-AF accumulates in cells while free AF does not. Int J Nanomedicine. 2017 Jan 13;12:577-591.
Human plasma 100 µg/mL 120 seconds To assess the effect of AEBSF on the direct fibrinogen cleaving actions of C. mictlantecuhtli venom, results showed that AEBSF inhibited this action. Front Immunol. 2021 Mar 11;12:612846.
Mono Mac 6 (MM6) cells 150 to 250 µM 18 hours AEBSF blocked Dicer proteolysis, resulting in increased full-length Dicer and decreased 170 kDa and 50 kDa fragments. Proc Natl Acad Sci U S A. 2020 Apr 14;117(15):8573-8583.
Human primary monocytes 250 µM 18 hours AEBSF treatment resulted in strong up-regulation of full-length Dicer and reduced the 50 kDa fragment. Proc Natl Acad Sci U S A. 2020 Apr 14;117(15):8573-8583.
Human retinal pigment epithelial cells (hRPE) 0-300 µM 2 hours Pretreatment with AEBSF significantly inhibited TM-induced mitochondrial permeability transition and cell death in hRPE cells Free Radic Biol Med. 2012 Sep 1;53(5):1111-22.
Keratinocytes 250 µM 20 hours AEBSF significantly inhibited TLSP activity in the stratum corneum. J Invest Dermatol. 2012 May;132(5):1435-42.
Uni-Graft prosthesis 0.6 mg/mL 3 hours Inhibition of adhesion and multiplication of Staphylococcus aureus and Candida albicans Biomolecules. 2020 Jan 4;10(1):82.
Human Umbilical Vein Endothelial Cells (HUVEC) 100 µM 4 hours AEBSF inhibited the ATF6 signaling pathway, blocking the sFRP2-mediated angiogenesis through cTGF, resulting in reduced tubule formation in HUVECs. Basic Res Cardiol. 2020 Jun 26;115(4):48.

AEBSF HCl 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
SFRP2 TG mice Permanent Coronary Artery Occlusion Model Osmotic Pump 2 μg/kg/day Once daily for 1 week AEBSF, by inhibiting the ATF6 signaling pathway, blocked the sFRP2-mediated cardioprotection and angiogenesis, resulting in the abolition of reduced infarct size and protection of cardiac function. Basic Res Cardiol. 2020 Jun 26;115(4):48.
Mice IL10-/- mice Oral gavage 300 mg/kg Starting from 1 day before V/M treatment and continuing during V/M treatment To assess the effect of AEBSF on V/M-induced high protease activity and intestinal barrier function, results showed that AEBSF significantly reduced protease activity and protected intestinal barrier function. Cell Mol Gastroenterol Hepatol. 2018 May 29;6(3):370-388.e3

AEBSF HCl 参考文献

[1]Citron M, et al. Inhibition of amyloid beta-protein production in neural cells by the serine protease inhibitor AEBSF. Neuron. 1996 Jul;17(1):171-9

[2]Nakabo Y, et al. Lysis of leukemic cells by human macrophages: inhibition by 4-(2-aminoethyl)-benzenesulfonyl fluoride (AEBSF), a serine protease inhibitor. J Leukoc Biol. 1996 Sep;60(3):328-36.

[3]Buitrago-Rey R, et al. Evaluation of two inhibitors of invasion: LY311727 [3-(3-acetamide-1-benzyl-2-ethyl-indolyl-5-oxy)propane phosphonic acid] and AEBSF [4-(2-aminoethyl)-benzenesulphonyl fluoride] in acute murine toxoplasmosis. J Antimicrob Chemother.

[4]Jiang YH, et al. Serine protease inhibitor 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF) inhibits the rat embryo implantation in vivo and interferes with cell adhesion in vitro. Contraception. 2011 Dec;84(6):642-8.

AEBSF HCl 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.17mL

0.83mL

0.42mL

20.86mL

4.17mL

2.09mL

41.72mL

8.34mL

4.17mL

AEBSF HCl 技术信息

CAS号30827-99-7
分子式C8H11ClFNO2S
分子量 239.69
SMILES Code O=S(C1=CC=C(CCN)C=C1)(F)=O.[H]Cl
MDL No. MFCD00132962
别名 AEBSF盐酸盐 ;AEBSF (hydrochloride); AEBSF HCl; Pefabloc SC
运输蓝冰
InChI Key WRDABNWSWOHGMS-UHFFFAOYSA-N
Pubchem ID 186136
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 105 mg/mL(438.06 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 100 mg/mL(417.2 mM)

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
方案 二
方案 三
配制的工作液建议现用现配,短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
方案 二
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