JAK2 Inhibitor V,Z3

  Cat. No.:  DC7436   Featured
Chemical Structure
195371-52-9
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Field of application
Z3(NSC 42834), a novel specific inhibitor of Jak2, inhibits Jak2-V617F and Jak2-WT autophosphorylation in a dose-dependent manner but was not cytotoxic to cells at concentrations that inhibited kinase activity.
Cas No.: 195371-52-9
Chemical Name: Z3; NSC 42834; 1-Butanone, 2-methyl-1-phenyl-4-(2-pyridinyl)-2-[2-(2-pyridinyl)ethyl]-
Synonyms: Z3; NSC 42834; 1-Butanone, 2-methyl-1-phenyl-4-(2-pyridinyl)-2-[2-(2-pyridinyl)ethyl]-
SMILES: C(C1=CC=CC=C1)(=O)C(C)(CCC1=NC=CC=C1)CCC1=NC=CC=C1
Formula: C23H24N2O
M.Wt: 344.5
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: JAK2 Inhibitor V, Z3 is a cell-permeable pyridinylbutanone compound that inhibits both JAK2 and the active V167F mutant cellular autophosphorylation. JAK2 Inhibitor V, Z3 displays no effect against cellular Tyk 2 autophosphorylation in COS cells or SRC in cell-free kinase assays. JAK2 Inhibitor V, Z3 suppresses the JAK2-V167F-dependent proliferation of the erythroleukemia cell line HEL by blocking the G1-S transition and is shown to effectively reduce the cytokine-stimulated growth of both Jak2-V617F-positive and Jak2-F537I-positive primary hematopoietic progenitor cells from myeloproliferative disorder patients.For the detailed information of JAK2 Inhibitor V, the solubility of JAK2 Inhibitor V in water, the solubility of JAK2 Inhibitor V in DMSO, the solubility of JAK2 Inhibitor V in PBS buffer, the animal experiment (test) of JAK2 Inhibitor V, the cell expriment (test) of JAK2 Inhibitor V, the in vivo, in vitro and clinical trial test of JAK2 Inhibitor V, the EC50, IC50,and Affinity of JAK2 Inhibitor V, Please contact DC Chemicals.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC7436 JAK2 Inhibitor V,Z3 Z3(NSC 42834), a novel specific inhibitor of Jak2, inhibits Jak2-V617F and Jak2-WT autophosphorylation in a dose-dependent manner but was not cytotoxic to cells at concentrations that inhibited kinase activity.
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