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Cat. No. Product Name Information
PC-22202

JAK3 inhibitor RB1

JAK3 inhibitor

JAK3 inhibitor RB1 is a potent, selective and irreversible JAK3 inhibitor with IC50 of 40 nM, without inhibiting JAK1, JAK2 or TYK2 (IC50>5000 nM).
PC-21900

CEP-33779

JAK2 inhibitor

CEP-33779 is a potent, selective, and orally bioavailable inhibitor of JAK2 with IC50 of 1.3 nM, 65-fold selective over JAK-3.
PC-21596

JNJ-64251330

JAK inhibitor

Lorpucitinib (JNJ-64251330) is potent, selective and orally bioavailable pan-JAK inhibitor with IC50 of 0.37/8.6/92/7.4 nM for JAK1/JAK2/JAK3/Tyk2 respectively.
PC-21425

WHI-P131

JAK3 inhibitor

WHI-P131 (JANEX-1) is a potent and selective JAK3 inhibitor with Ki of 2.3 uM and IC50 of 78 uM, with no activity agianst JAK1 and JAK2.
PC-21281

QL-1200186

TYK2-JH2 inhibitor

QL-1200186 is a potent, highly selective allosteric inhibitor of tyrosine kinase 2 (TYK2) with IC50 of 0.06 nM, targets pseudokinase regulatory domain (Janus homology 2, JH2) of the TYK2 protein.
PC-21215

GDC-4379

JAK inhibitor

GDC-4379 is a potent, selective and inhaled JAK inhibitor, reduces FeNO and peripheral biomarkers of inflammation.
PC-20901

YLIU-5-162-1

JAK2 inhibitor

YLIU-4-105-1 is a novel type II JAK2 inhibitor, binds to JAK2 kinase domain (JH1), show potential for overcoming acquired resistance to ruxolitinib.
PC-20543

ABT-317

JAK1 inhibitor

ABT-317 (ABT317) is a potent, selective JAK1 inhibitor, inhibits IL-6-stimulated pSTAT3 (TF-1 cells, IC50=16 nM) and IL-2-stimulated pSTAT5 (T-blasts, IC50=30 nM).
PC-72038

NDI-031407

TYK2 inhibitor

NDI-031407 (NDI 031407) is a novel potent, selective TYK2 inhibitor with IC50 of 0.21 nM in radiometric assays, 20 fold selectivity over JAK3 (4.2 nM), 147 fold for JAK2 (31 nM), and 220 fold for JAK1 (46 nM).
PC-61277

EXEL-8232

A potent and selective, orally bioavailable JAK2 inhibitor with IC50 of 2 nM.
PC-45873

Ruxolitinib S enantiomer

The chirality of Ruxolitinib (INCB-018424), which is a potent, selective, orally active JAK1/JAK2 inhibitor with IC50 of 3.3/2.8 nM, respectively..
PC-45817

Tofacitinib citrate

A potent, specific, orally active inhibitor of JAK3 with IC50 of 1 nM in cell-free assays.

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