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苄基磺酰氟 /PMSF {[allProObj[0].p_purity_real_show]}

货号:A767839 同义名: 苯甲基磺酰氟 / NSC 88499;Benzylsulfonyl fluoride Ambeed 开学季,买赠积分,赢豪礼

PMSF is a non-selective serine/cysteine protease inhibitor, also blocks anandamide metabolism.

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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+
PMSF 化学结构 CAS号:329-98-6
PMSF 化学结构
CAS号:329-98-6
PMSF 3D分子结构
CAS号:329-98-6
PMSF 化学结构 CAS号:329-98-6
PMSF 3D分子结构 CAS号:329-98-6
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PMSF 纯度/质量文件 产品仅供科研

货号:A767839 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

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产品名称 Cysteine Protease 其他靶点 纯度
Z-FA-FMK {[allProObj[0].p_purity_real_show]}
Leupeptin hemisulfate {[allProObj[0].p_purity_real_show]}
PMSF {[allProObj[0].p_purity_real_show]}
PD 151746 +

μ-Calpain, IC50: 260 nM

m-calpain, IC50: 5.33 μM

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Odanacatib ++++

Cathepsin K (human), IC50: 0.2 nM

Cathepsin K (rabbit), IC50: 1 nM

{[allProObj[0].p_purity_real_show]}
E-64 +++

Cysteine protease, IC50: 9 nM

{[allProObj[0].p_purity_real_show]}
E 64c {[allProObj[0].p_purity_real_show]}
E-64d {[allProObj[0].p_purity_real_show]}
MG-101 {[allProObj[0].p_purity_real_show]}
Calpeptin ++

Calpain II (porcine kidney), ID50: 40 nM

Calpain I (porcine erythrocytes), ID50: 52 nM

{[allProObj[0].p_purity_real_show]}
Cathepsin inhibitor 1 +++

Cathepsin L2, pIC50: 5.5

Cathepsin L, pIC50: 7.9

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1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 20S proteasome Proteasome 其他靶点 纯度
Ixazomib ++++

20S proteasome, IC50: 3.4 nM

20S proteasome, Ki: 0.93 nM

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Delanzomib +++

Chymotrypsin-like proteasome, IC50: 3.8 nM

{[allProObj[0].p_purity_real_show]}
Celastrol +

20S proteasome, IC50: 2.5 μM

{[allProObj[0].p_purity_real_show]}
MLN9708 +++

20S proteasome, IC50: 3.4 nM

20S proteasome, Ki: 0.93 nM

{[allProObj[0].p_purity_real_show]}
Bortezomib ++++

20S proteasome, Ki: 0.6 nM

{[allProObj[0].p_purity_real_show]}
Oprozomib ++

20S proteasome LMP7, IC50: 82 nM

20S proteasome β5, IC50: 36 nM

{[allProObj[0].p_purity_real_show]}
Epoxomicin {[allProObj[0].p_purity_real_show]}
PI-1840 ++

Chymotrypsin-like proteasome, IC50: 27 nM

{[allProObj[0].p_purity_real_show]}
VR23 +++

Chymotrypsin-like proteasomes, IC50: 3 μM

Trypsin-like proteasomes, IC50: 1 nM

{[allProObj[0].p_purity_real_show]}
Carfilzomib ++

Proteasome, IC50: 5 nM

{[allProObj[0].p_purity_real_show]}
(R)-MG-132 +

Proteasome, IC50: 100 nM

{[allProObj[0].p_purity_real_show]}
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

PMSF 生物活性

靶点
  • Cysteine Protease

描述 Phenylmethanesulfonyl fluoride (PMSF) is an irreversible serine/cysteine protease inhibitor used in protein extraction experiment. It is also a putative inhibitor of phosphatidylinositol-specific phospholipase C, almost completely inhibited carbachol-stimulated inositol incorporation into phosphatidylinositol (PI) of longitudinal smooth muscle of guinea pig ileum, while it had no effect on potassium-stimulated inositol incorporation. PMSF (2 mM) inhibited carbachol-stimulated inositol phosphate accumulation in the presence of Li+ by only 15% - 19%[3]. Mice receiving i.p. injections of PMSF exhibited cannabinoid effects that included antinociception, hypothermia and immobility with ED50 values of 86, 224 and 206 mg/kg, respectively. Spontaneous activity was reduced at doses greater than 100 mg/kg. On the other hand, pretreatment with an inactive dose of PMSF (30 mg/kg) potentiated the effects of anandamide on tail-flick response (antinociception), spontaneous activity and mobility by 5-, 10- and 8-fold, respectively. PMSF did not alter anandamide's hypothermic effects[4]. PMSF inhibits the acylation of the inositol residue of GPI intermediates in bloodstream form T. brucei. PMSF inhihits the formntion of glycolipid C but does not inhibit fatty acid remodeling in vitro. PMSF inhihits GPI acylation and ethanolamine phosphatp addition in procyclic trypanosomes but not in Hela cells[5].

PMSF 参考文献

[1]Estevez J, Barril J, et al. Kinetics of inhibition of soluble peripheral nerve esterases by PMSF: a non-stable compound that potentiates the organophosphorus-induced delayed neurotoxicity. Arch Toxicol. 2012 May;86(5):767-77.

[2]Sheth AR, Gunjikar AN, et al. The presence of progressive motility sustaining factor (PMSF) in human epididymis. Andrologia. 1981 Mar-Apr;13(2):142-6.

[3]Sekar MC, Roufogalis BD. Differential effects of phenylmethanesulfonyl fluoride (PMSF) on carbachol and potassium stimulated phosphoinositide turnover and contraction in longitudinal smooth muscle of guinea pig ileum. Cell Calcium. 1984;5(3):191-203

[4]Compton DR, Martin BR. The effect of the enzyme inhibitor phenylmethylsulfonyl fluoride on the pharmacological effect of anandamide in the mouse model of cannabimimetic activity. J Pharmacol Exp Ther. 1997;283(3):1138-1143

[5]Güther ML, Masterson WJ, Ferguson MA. The effects of phenylmethylsulfonyl fluoride on inositol-acylation and fatty acid remodeling in African trypanosomes. J Biol Chem. 1994;269(28):18694-18701

PMSF 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

5.74mL

1.15mL

0.57mL

28.70mL

5.74mL

2.87mL

57.41mL

11.48mL

5.74mL

PMSF 技术信息

CAS号329-98-6
分子式C7H7FO2S
分子量 174.193
别名 苯甲基磺酰氟 ;NSC 88499;Benzylsulfonyl fluoride;Phenylmethylsulfonyl fluoride
运输蓝冰
存储条件

粉末 Inert atmosphere,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 250 mg/mL(1435.19 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

动物实验配方
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