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JAK2-IN-7

Catalog No.GC62500

JAK2-IN-7 est un inhibiteur sélectif de JAK2 avec des IC50 de 3, 11,7 et 41 nM pour les cellules JAK2, SET-2 et Ba/F3V617F, respectivement. JAK2-IN-7 possède une sélectivité > 14 fois supérieure À JAK1, JAK3, FLT3. JAK2-IN-7 stimule l'arrêt du cycle cellulaire en phase G0/G1 et induit une cellapoptose tumorale. Activités antitumorales.

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JAK2-IN-7 Chemical Structure

Cas No.: 2593402-36-7

Taille Prix Stock Qté
10mM (in 1mL DMSO)
410,00 $US
En stock
5 mg
405,00 $US
En stock
10 mg
720,00 $US
En stock
25 mg
1 485,00 $US
En stock
50 mg
2 295,00 $US
En stock
100 mg
3 420,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

JAK2-IN-7 is a selective JAK2 inhibitor with IC50s of 3, 11.7, and 41 nM for JAK2, SET-2, and Ba/F3V617F cells, respectively. JAK2-IN-7 possesses >14-fold selectivity over JAK1, JAK3, FLT3. JAK2-IN-7 stimulates cell cycle arrest in the G0/G1 phase and induces tumor cellapoptosis. Antitumor activities[1].

JAK2-IN-7 (compound 13ac) (0-1000 nM; 2 hours) inhibits JAK2 and STAT5 phosphorylation in a dose-dependent manner in SET-2 and Ba/F3-JAK2V617F cells[1].JAK2-IN-7 (10-160 nM; 24 hours) induces cell arrest in the G0/G1 phase[1].JAK2-IN-7 (0.05-1.6 μM; 2 hours) induces apoptosis in SET-2 cells[1].

JAK2-IN-7 (15-60 mg/kg; p.o.; daily for 16 days) shows potent in vivo antitumor efficacy with 82.3% tumor growth inhibition in the SET-2 xenograft model[1].JAK2-IN-7 (30-60 mg/kg; p.o.; q.d. for 16 day) significantly ameliorates the disease symptoms in a Ba/F3-JAK2V617F allograft model, with 77.1% normalization of spleen weight, which was more potent than Ruxolitinib[1].

[1]. Yang T, et al. N-(Pyrimidin-2-yl)-1,2,3,4-tetrahydroisoquinolin-6-amine Derivatives as Selective Janus Kinase 2 Inhibitors for the Treatment of Myeloproliferative Neoplasms [published online ahead of print, 2020 Nov 30]. J Med Chem. 2020;10.1021/acs.jmedchem.0c01488.

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