| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
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). |
|
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. |
|
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. |
|
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. |
|
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. |
|
V136879 | GPR84 agonist-2 | 3105662-82-3 | GPR84 agonist-2 is a selective GPR84 agonist that is inactive against free fatty acid receptors. |
|
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. |
|
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. |
|
V140403 | MrgprX2-IN-2 | 2792205-87-7 | MrgprX2-IN-2 is a selective Mas-associated G protein-coupled receptor X2 (MRGPRX2) antagonist. |
|
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. |
|
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). | |
|
V144654 | SB-583355 | 3040121-49-8 | SB-583355 is a potent G2A antagonist. |
|
V144809 | Setomagpran | 2991434-57-0 | Setomagpran is an antagonist of mas-associated G protein-coupled receptors (MRGPR) and has anti-inflammatory activity. |
|
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. |
|
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). | |
|
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. |