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Cat. No. Product Name Information
PC-49391

Rytvela

IL-1RI inhibitor

Rytvela (Peptide 101.10, d-(RYTVELA)) is a potent, selective, allosteric negative modulator (antagonist) of IL-1 receptor I (IL-1RI), inhibits dose-dependently IL-1-induced PGE2 formation (IC50= 0.5 nM) and IL-1-induced human thymocyte (TF-1 cell) proliferation (IC50=2 nM).
PC-72919

A-552

L-36γ antagonist

A-552 (A552) is a potent, small molecule antagonist of human IL-36γ, exhibits Ki of 31/54 nM in IL-36γ evoked CXCL1 release in human/mouse cellular assays.
PC-72481

IL4 inhibitor 52

IL4 inhibitor

IL4 inhibitor 52 is the first IL-4 small-molecule inhibitor (EC50=1.81 uM) with potency for the cytokine and disrupts type II IL-4 signaling in cells.
PC-35897

LMT-28

IL-6 inhibitor

LMT-28 (LMT28) is a specific blocker of IL-6 signaling via inhibits IL-6Rβ (gp130) with IC50 of 5.9 uM (IL-6–induced luciferase activity), selectively inhibits IL-6–induced phosphorylation of STAT3, JAK2, and gp130.
PC-62479

SP4206

IL-2α receptor inhibitor

SP4206 is a high-affinity (Kd=70 nM) small molecule that blocks the binding of the IL-2α receptor (IL-2Rα) to IL-2.
PC-45128

Suplatast tosilate

Th2 cytokine inhibitor

Suplatast tosilate (IPD-1151T) is a Th2 cytokine inhibitor that attenuates IL-2, IL-5 and IL-13 production and has no effect on IFN-γ production.
PC-45769

YM-90709

IL-5 receptor inhibitor

YM-90709 (YM90709) is a potent IL-5 receptor antagonist that inhibits the binding of IL-5 to its receptor on peripheral human eosinophils and butyric acid-treated eosinophilic HL-60 clone 15 cells with IC50 of 1.0 and 0.57 uM, respectively.
PC-22797

JNJ-77242113

IL-23 receptor inhibitor

JNJ-77242113 is a highly potent, selective, oral peptide inhibitor of IL-23 receptor with Kd of 7.1 pM, potently and selectively inhibits proximal IL-23 signaling (IC50=5.6 pM) without impacting IL-12 signaling.
PC-21192

hIL-1β antagonist Compound (S)-2

hIL-1β antagonist

Compound (S)-2 is a specific antagonist of the hIL-1β /IL-1R1 (human interleukin-1β/IL-1R1) interaction with IC50 of 4.0 uM in TR-FRET assays, binds hIL-1β with SPR Kd of 1.1 uM.
PC-20616

Bindarit

MCP-1 inhibitor

Bindarit (AF2838) is a selective inhibition of inflammatory chemokine MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8, shows immunosuppressive effects anti-inflammatory activity.

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