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首页-小分子抑制剂&激动剂-GPCR-Vasoactive intestinal peptide receptor (VIPR)

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Cat. No. Product Name Information
PC-20662

VIPR1 antagonist 41

VIPR1 antagonist

VIPR1 antagonist 41 is a potent, selective vsoactive intestinal peptide receptor-1 (VIPR1) antagonist with cAMP IC50 of 0.29 uM.
PC-20660

Ro 25-1553

VIPR2 agonist

Ro 25-1553 is a potent, selective VIPR2 agonist and a cyclic peptide analog of vasoactive intestinal peptide (VIP), displaces the radioligand 125I-VIP from rat forebrain membranes with IC50 of 4.98 nM.
PC-20659

KS-133

VIPR2 antagonist

KS-133 (KS133) is a potent, selective bicyclic peptide antagonist of vasoactive intestinal peptide receptor 2 (VIPR2) with IC50 of 24.8 nM in Ca influx assays.
PC-49382

PA-915

PAC1 receptor antagonist

PA-915 (PA915) is a small-molecule, non-peptide antagonist of the PACAP type I (PAC1) receptor, inhibits PACAP (1 nM)-induced phosphorylation of CREB in PAC1/CHO cells with IC50 of <10 pM.
PC-72883

PA-8

PAC1 antagonist

PA-8 (PAC1 antagonist PA-8) is a potent, specific small molecule antagonist of PACAP type I (PAC1) receptor.
PC-20945

BAY 2686013

PAC1 receptor antagonist

BAY 2686013 is a selective, allosteric antagonist of human pituitary adenylate cyclase activating polypeptide receptor (hPAC1-R) with IC50 of 0.92 and 0.4 uM in cAMP HTRF and Ca2+ release assays, respectively.
PC-20663

VPAC2 antagonist 1

VIPR2 antagonist

VPAC2 antagonist 1 is a small molecule human vsoactive intestinal peptide receptor-2 (hVIPR2, hVPAC2 receptor) antagonist, inhibits VPAC2-mediated cAMP accumulation with IC50 of 3.8 uM and the ligand-activated beta-arrestin2 binding with IC50 of 2.3 uM.
PC-20661

BAY 55-9837

VIPR2 agonist

BAY 55-9837 is a potent, highly selective peptide agonist of vasoactive intestinal peptide receptor 2 (VIPR2, VPAC2 receptor) with Kd of 0.65 nM, >100-fold selectivity over VPAC1.

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