PF-06260933

目录号: GC31675纯度: >98.00%同义词: PF-06260933
A MAP4K4 inhibitor

PF-06260933
Cas No.: 1811510-56-1
规格价格库存数量操作
5mg¥1,071.00现货
1
10mg¥1,696.00现货
1
25mg¥3,481.00现货
1
50mg¥4,909.00现货
1
100mg¥7,586.00现货
1
10mM (in 1mL DMSO)¥1,178.00现货
1

文献被引

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产品描述 Description

PF-6260933 is an inhibitor of mitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4; IC50 = 3.7 nM).1 It is selective for MAP4K4 over a panel of 41 kinases at 1 ?M but also inhibits TRAF2- and NCK-interacting kinase (TNIK) and misshapen-like kinase 1 (MINK1; IC50s = 15 and 8 nM, respectively). PF-6260933 inhibits the replication of CMV strains AD169 and Merlin(R1111) strains in human foreskin fibroblast (HFF) cells (EC50s = 9.6 and 13.3 ?M, respectively).2 It inhibits collagen- or thrombin-induced aggregation of isolated human platelets by 70.9 and 61.2%, respectively, when used at a concentration of 20 ?M.3 It decreases plaque formation in ApoE-/- mice fed a Western diet in a model of atherosclerosis when administered at a dose of 10 mg/kg.4 PF-6260933 (15 mg/kg) decreases LPS-induced increases in TNF-α levels in wild-type mice and fasting blood glucose levels in ob/ob mice.1

1.Ammirati, M., Bagley, S.W., Bhattacharya, S.K., et al.Discovery of an in vivo tool to establish proof-of-concept for MAP4K4-based antidiabetic treatmentACS Med. Chem. Lett.6(11)1128-1133(2015) 2.Strang, B.L., Asquith, C.R.M., Moshrif, H.F., et al.Identification of lead anti-human cytomegalovirus compounds targeting MAP4K4 via machine learning analysis of kinase inhibitor screening dataPLoS One13(7)e0201321(2018) 3.Nam, G.S., Kim, S., Kwon, Y.-S., et al.A new function for MAP4K4 inhibitors during platelet aggregation and platelet-mediated clot retractionBiochem. Pharmacol.188114519(2021) 4.Roth Flach, R.J., Skoura, A., Matevossian, A., et al.Endothelial protein kinase MAP4K4 promotes vascular inflammation and atherosclerosisNat. Commun.68995(2015)

实验参考方法 Experimental Reference Method

Cell experiment:

HUVECs are maintained in EGM2 media at 37°C and 5% CO2. HUVECs or peritoneal macrophages are treated with vehicle or PF-06260933 in vitro to determine whether pharmacological inhibition of MAP4K4 alteres MAPK signalling in response to TNF-α[2].

Animal experiment:

Compound PF-06260933 (10 mg/kg, dissolved in dH2O) is orally administered to 8 to 10-week-old male Apoe-/- mice twice daily for 6 weeks. Ldlr-/- male mice are placed on high-fat diet (HFD) for 10 weeks before drug administration. Compound PF-06260933 is administered to male 8 to 10-week-old Ldlr-/- mice as above for 10 weeks. Oral administration of water is used as vehicle control in all studies. Mice are euthanized by CO2 inhalation followed by bilateral pneumothorax[2].

References:

[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.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
1811510-56-1
同义词
PF-06260933
SMILES
NC1=C(C2=CC=C(Cl)C=C2)C=C(C(C=N3)=CC=C3N)C=N1
分子式
C16H13ClN4
分子量
296.75 g/mol
溶解性
DMSO : 30 mg/mL (101.10 mM)
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol