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GPR

GPR

GPR related products

Structure Cat No. Product Name CAS No. Product Description
[Ala17]-MCH V70558 [Ala17]-MCH 359784-84-2 [Ala17]-MCH is an analog of MCH and is a ligand for MCHR1 (Ki=0.16 nM) with greater selectivity for MCHR2 (Ki=34 nM).
AZD1981 V1806 AZD1981 802904-66-1 AZD1981 is a novel potent and selective CRTh2 (Chemoattractant receptor-homologous molecule expressed on TH2 cells; DP2-Prostaglandin D2 receptor 2, ) receptor antagonist with IC50 of 4 nM,it displayed>1000-fold selectivity over more than 340 other enzymes and receptors, including DP1.
EP-3945 V135144 EP-3945 3057176-00-5 EP-3945 is a potent Mas-associated G protein-coupled receptor (MRGPR) agonist, which is more potent than the MRGPRD small molecule agonist β-alanine.
Gpr35 modulator 1 V93588 Gpr35 modulator 1 2994189-01-2 Gpr35 modulator 1 (compound 1-18) is a potent modulator of Gpr35 with IC50 ≤100 nM in HEK293 cells stably transfected with human GPR35.
GPR40激动剂类降糖药Fasiglifam V1803 Fasiglifam (TAK875) 1000413-72-8 Fasiglifam(formerly known as TAK-875; TAK875) is a novel, long-acting, selective and orally bioavailable GPR40 agonist with anti-diabetic activity.
GPR84 agonist-2 V136879 GPR84 agonist-2 3105662-82-3 GPR84 agonist-2 is a selective GPR84 agonist that is inactive against free fatty acid receptors.
GSK1292263 V1804 GSK1292263 1032823-75-8 GSK1292263 is a novel and potentGPR119 (G-protein-coupled receptor 119) agonist whichhas potential for the treatment of type 2 diabetes.
GW9508 V1805 GW9508 885101-89-3 GW9508 is a novel, potent and selective agonist for FFA1 (fatty acid receptor GPR40) with pEC50 of 7.32, and is 100-fold selective against GPR120, it stimulates insulin secretion in a glucose-sensitive manner.
MrgprX2-IN-2 V140403 MrgprX2-IN-2 2792205-87-7 MrgprX2-IN-2 is a selective Mas-associated G protein-coupled receptor X2 (MRGPRX2) antagonist.
RGH-706 V144075 RGH-706 2027497-52-3 RGH-706 is an orally effective, selective MCH1 receptor antagonist that crosses the blood-brain barrier, with an IC50 value of 6.2 nM for hMCHR1.
RTI-122 dihydrochloride V144403 RTI-122 dihydrochloride RTI-122 dihydrochloride is a selective, blood-brain barrier-crossing GPR88 agonist (cAMP EC50 = 11 nM), with EC50 values of 11.5 nM and 155 nM for human and mouse GPR88, respectively ([35S]GTPγS assay).
SB-583355 V144654 SB-583355 3040121-49-8 SB-583355 is a potent G2A antagonist.
Setomagpran V144809 Setomagpran 2991434-57-0 Setomagpran is an antagonist of mas-associated G protein-coupled receptors (MRGPR) and has anti-inflammatory activity.
Timapiprant (OC000459) V1807 Timapiprant (OC000459) 851723-84-7 Timapiprant (formerly known as OC000459; OC-000459) is a novel, potent, selective, and orally bioactive prostanoid receptor 2 (DP2- also known as CRTH2)) antagonist with IC50 of 13 nM.
TMN-OMe V146185 TMN-OMe TMN-OMe is a GPR39 agonist that can cross the blood-brain barrier and is also a radiotracer used in positron emission tomography (PET).
Zelatriazin (TAK-041; NBI-1065846) V70308 Zelatriazin (TAK-041; NBI-1065846) 1929519-13-0 Zelatriazin (TAK-041; NBI-1065846) is a potent and specific GPR139 agonist/activator with EC50 of 22 nM.
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