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Cat. No. Product Name Information
PC-27425

Fadeucravacitinib

TYK2 inhibitor

Fadeucravacitinib (ICP-488) is a potent and selective, allosteric TYK2 inhibitor with IC50 of 5.7 nM for TYK2-JH2, blocks the signal transduction of IL-23, IL-12, type 1 IFN and other inflammatory cytokine, thereby inhibiting the pathological process of autoimmune and inflammatory diseases.
PC-27421

Embricitinib

JAK inhibitor

Embricitinib is a potent, selective JAK1 inhibitor with IC50 of 0.15 nM, 3.69 nM, 3.10 nM and 1.49 nM for JAK1, JAK2, JAK3 and TYK2 respectively.
PC-27420

Durocitinib

TYK2 inhibitor

Durocitinib is a potent, selective TYK2 inhibitor.
PC-27282

TYK2 activator 6g

TYK2 activator

TYK2 activator 6g is a potent, selective small molecule TYK2 activator with EC50 of 0.21 uM (JH1/JH2 TYK2), maximal activation effect (Emax) of 7.8-fold.
PC-27281

HHT-9041P1

JAK1 inhibitor

HHT-9041P1 is a potent and selective JAK1 inhibitor with IC50 of 612 nM, displays 10-, 23- and 63-fold selective over JAK2, JAK3 and TYK2.
PC-26418

YYSW001

JAK1 inhibitor

YYSW001 is a potent, highly selective and orally bioavailable JAK1 inhibitor with IC50 of 6 nM, with no activity against JAK2 and JAK3.
PC-26362

Vexicitinib

JAK/SYK inhibitor

Vexicitinib (SYHX1901) is a potent, selective dual JAK/SYK inhibitor, interrupts both the IL-23/IL-17 axis and B-cell-dependent amplification loops, shows anti-inflammatory and immunosuppressant activities.
PC-26345

Nomelcitinib

Tyk2 inhibitor

Nomelcitinib (D-2570) is a potent, selective tyrosine kinase 2 (TYK2) inhibitor, selectively binds to the JH2 domain of TYK2.
PC-26282

H018

JAK1/2 inhibitor

H018 (RAI-20) is a highly potent, selective JAK1/2 inhibitor with IC50 of 15.1/22.7 nM, >10-fold and 20-fold selective over JAK3 amd TYK2, displays robust anti-arthritic efficacy.
PC-26072

ARTS-011

Tyk2 inhibitor

ARTS-011 is a potent, selective, allosteric and oral inhibitor of Tyk2, selectively targeting the JH2 domain of the Tyk2 protein.
PC-26017

NS-229

JAK1 inhibitor

NS-229 is a potent, selective JAK1 inhibitor with IC50 of 52 nM.
PC-25681

OB756

JAK2 inhibitor

OB756 (Bonretinib) is a potent, selective, oral JAK2 kinase inhibitor, inhibits cell proliferation and induces cell apoptosis, significantly inhibits the phosphorylation activity of p-STAT3 in the JAK-STAT signaling pathway.

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