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首页-小分子抑制剂&激动剂-GPCR-Lysophospholipid Receptor

Request The Product List ofLysophospholipid Receptor Lysophospholipid Receptor

Cat. No. Product Name Information
PC-42950

Ozanimod

S1P1/S1P5 agonist

Ozanimod (RPC-1063) is a potent, selective agonist of S1P1 and S1P5 receptor with EC50 of 0.41 nM and 11 nM respectively.
PC-42341

Icanbelimod

S1PR1 agonist

Icanbelimod (CBP-307) is a highly potent, next-generation highly potent sphingosine-1-phosphate receptor (S1PR) agonist with EC50 of 3.55 nM (S1PR1), specifically targets S1PR1/4/5.
PC-45386

Cenerimod

S1P1 agonist

Cenerimod (ACT-334441) is a potent and orally available S1P1 receptor agonist with EC50 of 2.7 nM.
PC-45066

Amiselimod hydrochloride

S1P1 modulator

Amiselimod (MT-1303) hydrochloride is a prodrug S1P1 receptor modulator lacking S1P3 receptor agonism to avoid bradycardia associated with fingolimod and other S1P receptor modulators.
PC-42284

ONO-7300243

LPA1 inhibitor

ONO7300243 is a novel potent, selective, orally available lysophosphatidic acid receptor 1 (LPA1) antagonist with IC50 of 0.16 uM.
PC-42379

CYM-5541

S1P3 agonist

CYM-5541 (ML249) is a potent, selective, allosteric and full agonist of S1P3 receptor with EC50 of 72-132 nM.
PC-23606

AS2717638

LPA5 antagonist

AS2717638 a potent, selective lysophosphatidic acid receptor 5 (LPA5, LPAR5) antagonist, inhibits LPA-induced cAMP accumulation in CHO cells expressing human LPA5 with IC50 of 38 nM.
PC-23559

GS-2278

LPAR1 antagonist

GS-2278 is a potent, selective lysophosphatidic acid receptor 1 (LPAR1, LPA1) antagonist with EC50 of 12 nM in MRTF-A nuclear translocation assay in TWNT4 cells.
PC-23526

AUY954 hydrochloride

S1P1 agonist

AUY954 hydrochloride is a potent, selective sphingosine-1-phosphate (S1P1) receptor agonist with EC50 of 1.2 nM (hS1P1) and 0.9 nM (mS1P1) in γ-GTPS-binding assays, >280-fold selective over S1P2-5.
PC-23525

AUY954

S1P1 agonist

AUY954 is a potent, selective sphingosine-1-phosphate (S1P1) receptor agonist with EC50 of 1.2 nM (hS1P1) and 0.9 nM (mS1P1) in γ-GTPS-binding assays, >280-fold selective over S1P2-5.
PC-23381

LPA1 agonist CpX

LPA1 agonist

LPA1 agonist CpX is a potent, selective agonist of lysophosphatidic acid receptor LPA1 with pEC50 of 5.6 in cell-based calcium mobilization assay, has 30-fold higher agonistic activity as compared with LPA.
PC-23380

LPA1 agonist CpY

LPA1 agonist

LPA1 agonist CpY is a potent, selective agonist of lysophosphatidic acid receptor LPA1 with pEC50 of 6.3 in cell-based calcium mobilization assay, has 30-fold higher agonistic activity as compared with LPA.

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