货号:A767839 同义名: 苯甲基磺酰氟 / NSC 88499;Benzylsulfonyl fluoride
PMSF is a non-selective serine/cysteine protease inhibitor, also blocks anandamide metabolism.
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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+ |
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产品名称 | Cysteine Protease ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Z-FA-FMK | ✔ | 99%+ | |||||||||||||||||
Leupeptin hemisulfate | ✔ | 97% | |||||||||||||||||
PMSF | ✔ | 95% | |||||||||||||||||
PD 151746 |
+
m-calpain, IC50: 5.33 μM μ-Calpain, IC50: 260 nM |
98% | |||||||||||||||||
Odanacatib |
++++
Cathepsin K (rabbit), IC50: 1 nM Cathepsin K (human), IC50: 0.2 nM |
99%+ | |||||||||||||||||
E-64 |
+++
Cysteine protease, IC50: 9 nM |
99%+ | |||||||||||||||||
E 64c | ✔ | 95% | |||||||||||||||||
E-64d | ✔ | 99%+ | |||||||||||||||||
MG-101 | ✔ | 98%+ | |||||||||||||||||
Calpeptin |
++
Calpain II (porcine kidney), ID50: 40 nM Calpain I (porcine erythrocytes), ID50: 52 nM |
98%+ | |||||||||||||||||
Cathepsin inhibitor 1 |
+++
Cathepsin L2, pIC50: 5.5 Cathepsin L, pIC50: 7.9 |
98% | |||||||||||||||||
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 |
99%+ | |||||||||||||||||
Delanzomib |
+++
Chymotrypsin-like proteasome, IC50: 3.8 nM |
98% | |||||||||||||||||
Celastrol |
+
20S proteasome, IC50: 2.5 μM |
98% | |||||||||||||||||
MLN9708 |
+++
20S proteasome, IC50: 3.4 nM 20S proteasome, Ki: 0.93 nM |
99% | |||||||||||||||||
Bortezomib |
++++
20S proteasome, Ki: 0.6 nM |
98% | |||||||||||||||||
Oprozomib |
++
20S proteasome LMP7, IC50: 82 nM 20S proteasome β5, IC50: 36 nM |
99%+ | |||||||||||||||||
Epoxomicin | ✔ | 99% | |||||||||||||||||
PI-1840 |
++
Chymotrypsin-like proteasome, IC50: 27 nM |
98% | |||||||||||||||||
VR23 |
+++
Trypsin-like proteasomes, IC50: 1 nM Chymotrypsin-like proteasomes, IC50: 3 μM |
98% | |||||||||||||||||
Carfilzomib |
++
Proteasome, IC50: 5 nM |
98% | |||||||||||||||||
(R)-MG-132 |
+
Proteasome, IC50: 100 nM |
98% | |||||||||||||||||
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。 |
靶点 |
|
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]. |
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 |
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 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Inert atmosphere,Room Temperature |
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 |