>>Signaling Pathways>> Microbiology & Virology>> Virus Protease>>PF429242 dihydrochloride

PF429242 dihydrochloride

Catalog No.GC36884

PF429242 이염산염은 IC50이 175nM인 가역적이고 경쟁력 있는 SREBP 부위 1 프로테아제(S1P) 억제제입니다.

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PF429242 dihydrochloride Chemical Structure

Cas No.: 2248666-66-0

Size 가격 재고 수량
10mM (in 1mL DMSO)
US$87.00
재고 있음
1mg
US$30.00
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5mg
US$79.00
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10mg
US$117.00
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25mg
US$248.00
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50mg
US$360.00
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100mg
US$531.00
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Sample solution is provided at 25 µL, 10mM.

Description of PF429242 dihydrochloride

PF429242 dihydrochloride is a reversible and competitive S1P inhibitor with an IC50 of 175 nM.

10 μM PF-429242 inhibits endogenous SREBP processing in Chinese hamster ovary cells. PF-429242 also down-regulates the signal from an SRE-luciferase reporter gene in human embryonic kidney 293 cells and the expression of endogenous SREBP target genes in cultured HepG2 cells. In HepG2 cells, PF-429242 inhibits cholesterol synthesis, with an IC50 of 0.5 μM[1]. The addition of PF-429242 (30 μM) shows statistically significant suppression of infectious viral titers and viral RNA copies in the cell culture fluids. PF-429242 treatment also shows suppressive effects on DENV2 yields in the cultured fluids of human-derived HEK-293, Hep G2, and non-human-primate derived LLC-MK2 cells[2]. PF-429242 efficiently prevents the processing of GPC from the prototypic arenavirus lymphocytic choriomeningitis virus (LCMV) and LASV, which correlates with the compound's potent antiviral activity against LCMV and LASV in cultured cells[3].

In mice treated with PF-429242 for 24 h, the expression of hepatic SREBP target genes is suppressed, and the hepatic rates of cholesterol and fatty acid synthesis are reduced[1].

References:
[1]. Hawkins JL, et al. Pharmacologic inhibition of site 1 protease activity inhibits sterol regulatory element-binding protein processing and reduces lipogenic enzyme gene expression and lipid synthesis in cultured cells and experimental animals. J Pharmacol Exp Ther. 2008 Sep;326(3):801-8.
[2]. Uchida L, et al. Suppressive Effects of the Site 1 Protease (S1P) Inhibitor, PF-429242, on Dengue Virus Propagation. Viruses. 2016 Feb 10;8(2). pii: E46. doi: 10.3390/v8020046.
[3]. Urata S, et al. Antiviral activity of a small-molecule inhibitor of arenavirus glycoprotein processing by the cellular site 1 protease. J Virol. 2011 Jan;85(2):795-803.

Chemical Properties of PF429242 dihydrochloride

Cas No. 2248666-66-0 SDF
Canonical SMILES O=C(N(CCC1=CC=CC=C1OC)[C@H]2CNCC2)C3=CC=C(CN(CC)CC)C=C3.[H]Cl.[H]Cl
Formula C25H37Cl2N3O2 M.Wt 482.49
Solubility DMSO: ≥ 83.3 mg/mL (172.65 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of PF429242 dihydrochloride

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1 mg 5 mg 10 mg
1 mM 2.0726 mL 10.3629 mL 20.7258 mL
5 mM 0.4145 mL 2.0726 mL 4.1452 mL
10 mM 0.2073 mL 1.0363 mL 2.0726 mL
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Review for PF429242 dihydrochloride

Average Rating: 5 ★★★★★ (Based on Reviews and 35 reference(s) in Google Scholar.)

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