الصفحة الرئيسية>>Signaling Pathways>> MAPK Signaling>> MAP4K>>PF-06260933

PF-06260933 (Synonyms: PF-06260933)

رقم الكتالوجGC31675

PF-06260933 هو مثبط فعال عن طريق الفم وانتقائي للغاية لـ MAP4K4 مع IC50s من 3.7 و 160 نانومتر للكيناز والخلية ، على التوالي

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PF-06260933 التركيب الكيميائي

Cas No.: 1811510-56-1

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
122٫00
متوفر
5mg
110٫00
متوفر
10mg
175٫00
متوفر
25mg
358٫00
متوفر
50mg
506٫00
متوفر
100mg
782٫00
متوفر

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مراجعات العميل

بناء على آراء العملاء.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

PF-06260933 is a highly selective small-molecule inhibitor of MAP4K4 with IC50s of 3.7 and 160 nM for kinase and cell, respectively.

PF-06260933 treatment of human aortic endothelial cell (EC) robustly prevents TNF-α-mediated endothelial permeability in vitro, similar to MAP4K4 knockdown[2].

In the mice model, PF-06260933 treatment does not alter plasma lipid content, although reductions in glucose levels are observed, which is consistent with whole-body-inducible Map4k4 knockout animals. PF-06260933 administration ameliorates further plaque development and/or promotes plaque regression in this animal model (46.0% versus 25.5%), and a reduction in plasma glucose as well as lipid content is also observed[2].

[1]. Ammirati M, et al. Discovery of an in Vivo Tool to Establish Proof-of-Concept for MAP4K4-Based Antidiabetic Treatment. ACS Med Chem Lett. 2015 Oct 6;6(11):1128-33. [2]. Roth Flach RJ, et al. Endothelial protein kinase MAP4K4 promotes vascular inflammation and atherosclerosis. Nat Commun. 2015 Dec 21;6:8995.

مراجعات

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