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Pifithrin-α

    
98.00%

Pifithrin-α

源叶(MedMol)
S81505 一键复制产品信息
63208-82-2
C16H18N2OS.HBr
367.30
吡菲他林-α
Pifithrin-α(63208-82-2)
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81505-5mg
98.00%

¥200.00

2 - - - -
S81505-10mg
98.00%

¥280.00

8 - - - -
S81505-25mg
98.00%

¥520.00

1 - - - -
S81505-50mg
≥98%

¥900.00

货期:2-3天 - - - -
S81505-100mg
98.00%

¥1500.00

1 - - - -
产品描述: Pifithrin-α hydrobromide is a p53 inhibitor which blocks its transcriptional activity and prevents cells from apoptosis. Pifithrin-α hydrobromide is also an aryl hydrocarbon receptor (AhR) agonist.
靶点: p53 AhR;Ferroptosis; ArylHydrocarbonReceptor; p53
体内研究: When the experiment is performed with Pifthirin-α (PFT-α) hydrobromide, a pharmacological p53 inhibitor, the percentage of annexin V-positive Foxe3-/- SMCs decreases to WT levels. Pifithrin-α (2.2 mg/kg, i.p.) significantly reduces the incidence of aortic rupture and intramural hematomas in Foxe3-/- mice that underwent transverse aortic constriction (TAC) (50% to 17%, P<0.05). After Pifthirin-α treatment, the mean diameter of the ascending aorta and the percentage of TUNEL-positive cells in the aortic media are also normalized to WT levels in surviving Foxe3-/- animals (P<0.05)
参考文献: 1. Yu W, et al. Cyclosporine A Suppressed Glucose Oxidase Induced P53 Mitochondrial Translocation and Hepatic Cell Apoptosis through Blocking Mitochondrial Permeability Transition. Int J Biol Sci. 2016 Jan 1;12(2):198-209. 2. Hoagland MS, et al. The p53 Inhibitor Pifithrin-α Is a Potent Agonist of the Aryl Hydrocarbon Receptor. J Pharmacol Exp Ther. 2005 Aug;314(2):603-10. 3. Kuang SQ, et al. FOXE3 mutations predispose to thoracic aortic aneurysms and dissections. J Clin Invest. 2016 Mar 1;126(3):948-61.
溶解性: DMSO  :  ≥  50  mg/mL  (136.13  mM)    H2O  :  1.25  mg/mL  (3.40  mM;  Need  ultrasonic)
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.723 ml 13.613 ml 27.226 ml
5 mM 0.545 ml 2.723 ml 5.445 ml
10 mM 0.272 ml 1.361 ml 2.723 ml
50 mM 0.054 ml 0.272 ml 0.545 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

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