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Cat. No. Product Name Information
PC-22735

KSI-6666

S1P1 antagonist

KSI-6666 is a potent and selective competitive antagonist of sphingosine 1-phosphate receptor 1 (S1PR1, S1P1 receptor) with IC50 of 6.4 nM in GTP binding assay, and IC50 of 2.64 nM in in Ca2+ mobilization assays.
PC-22065

ESB1609

S1P5 agonist

ESB1609 is a potent, selective, next-generation S1P5 receptor agonist with EC50 of 70 nM at the human S1P5 receptor, has >700-fold selectivity over human S1P1, S1P2, S1P3, and S1P4 receptors (EC50>5 uM).
PC-21751

ACT-1016-0707

LPA1 inhibitor

ACT-1016-0707 is a potent, selective, and orally active lysophosphatidic acid receptor subtype 1 receptor (LPA1 receptor, LPAR1) antagonist with IC50 of 3.1 nM, highly selective over LPAR2 or LPAR3.
PC-21569

LPA1 antagonist HL001

LPA1 antagonist

HL001 is a novel lysophosphatidic acid 1 (LPA1) receptor antagonist, suppresses fibrosis-associated subpopulations of fibroblasts, exhibits significant anti-fibrotic effects both in murine models and human organoid models.
PC-21441

NXC736 hydrochloride

S1PR4 inhibitor

NXC736 (Vonifimod, SLB736) hydrochloride is a selective functional antagonist for type 4 sphingosine-1-phosphate receptor (S1PR4, S1P4 receptor), has immunomodulatory and anti-fibrotic effects.
PC-21440

NXC736

S1P4 antagonist

NXC736 (Vonifimod, SLB736) is a selective functional antagonist for type 4 sphingosine-1-phosphate receptor (S1P4 receptor, S1P4R), has immunomodulatory and anti-fibrotic effects.
PC-21209

TY-52156

S1P3 inhibitor

TY-52156 is a potent, selective S1P3 receptor antagonist with Ki of 110 nM.
PC-21122

TP0541640

LPA1 antagonist

TP0541640 (TP 0541640) is a novel potent LPA1 antagonist with IC50 of 1.6 nM, shows potential for the treatment of lung and skin fibrosis.
PC-20833

A-971432

S1P5 agonist

A-971432 is a potent, highly selective, CNS-penetrant and orally bioavailable agonist of S1P5 receptor with EC50 values of 4.1 and 5.7 nM in cAMP and GTPγS assays, respectively.
PC-20759

ONO-0740556

LPA1 agonist

ONO-0740556 is a small molecule agonist of lysophosphatidic acid receptor 1 (LPA1) with EC50 of 0.26 nM (human LPA1), ONO-0740556 is an LPA analog with more potent activity against LPA1.
PC-20462

LPA2 antagonist 58

LPA2 inhibitor

LPA2 antagonist 58 is a highly potent and selective LPA2 receptor antagonist with pIC50 of 8.22 (hLPA2) and 8.19 (mLPA2), >1000-fold selectivity over LPA1 receptor.
PC-20419

SLB1122168 hydrochloride

Spns2 inhibitor

SLB1122168 hydrochloride is a potent, specific inhibitor of S1P transporter spinster homologue 2 (Spns2), inhibits Spns2-mediated S1P release with IC50 of 94 nM.

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