| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V125529 | 3-MPPI | 133399-65-2 | 3-MPPI is a G protein-coupled receptor (GPCR) ligand with high selectivity for α1-adrenergic receptors. Its Ki value for α1-adrenergic receptors is 0.21 nM, and its Ki value for 5-HT1A receptors is 50 nM. |
|
V144068 | RG-239 | 1199222-56-4 | RG-239 is an orally effective TGR5 agonist with an EC50 value of 120 nM, which is significantly better than betulinic acid (EC50 = 1.04 μM). |
|
V145277 | SSTR5/TGR5-modulator-1 | 3069267-46-2 | SSTR5/TGR5-modulator-1 is an orally effective dual-target small molecule that exhibits balanced activity against both human TGR5 and human SSTR5 in vitro. |
|
V15922 | TC-G 1005 | 1415407-60-1 | TC-G 1005 (TC-G-1005; TCG1005) is a novel, oral and potent TGR5 (GPBAR1) agonist with glucose-lowering effects. |
|
V145971 | TGR5 agonist 10 | 3081614-92-5 | TGR5 agonist 10 is a selective, allosteric, and orally effective Takeda G protein-coupled receptor 5 (TGR5) agonist with EC50 values of 0.8 μM for human TGR5 and 0.6 μM for mouse TGR5. |
|
V145972 | TGR5 agonist 7 | TGR5 agonist 7 is an intestinal-restricted, orally effective G protein-coupled bile acid receptor TGR5 (GPBAR1 or GPR131) agonist with an EC50 < 1 μM. | |
|
V2862 | TGR5 Receptor Agonist | 1197300-24-5 | TGR5 Receptor Agonist is a novel, potent andsynthetic small molecule agonist of TGR5 (G-protein coupled receptor19, GPCR19), it showed improved potency in the U2-OS cell assay with pEC50 of 6.8 and in melanophore cells with pEC50 of 7.5. |