GPCR/G protein
All GPCRs share a common seven trans-membrane structure. GPCRs are associated with heterotrimeric G-proteins which are GTP-binding proteins made of alpha, beta, and gamma subunits. When a ligand binds to GPCR, it activates the attached G-protein, the GDP is replaced with GTP. The activated G-protein then dissociates into an alpha and a beta-gamma complex which activates downstream signaling pathways. These intracellular signaling pathways include cAMP/PKA, calcium/NFAT, phospholipase C, protein tyrosine kinases, MAP kinases, PI-3-kinase, nitric oxide/cGMP, Rho, and JAK/STAT.
GPCRs are one of the most important therapeutic targets for various diseases, over 30% of all modern medicinal drugs target this family. Aberrant GPCR functions are involved in pathological conditions such as neurological, immunological and hormonal disorders. A large number of GPCRs have been identified, but whose ligands are not known, are classified as orphan receptors.
- B4876 K-Ras(G12C) inhibitor 12Summary: allosteric inhibitor of K-Ras(G12C)
- A8886 UNBS 5162Summary: A pan-antagonist of CXCL chemokines
- A1295 Granisetron HClSummary: 5-HT3 receptor antagonist
- A1334 Mosapride CitrateTarget: 5-HT3 Receptors|5-HT4 ReceptorsSummary: 5-HT receptor agonist
- A5010 AsenapineSummary: Inhibits adrenergic receptor/5-HT receptor
- A2884 Doxazosin MesylateSummary: α1-adrenergic receptor antagonist
- A2436 Fluoxetine HClTarget: Serotonin (5-HT) reuptakeSummary: Serotonin reuptake inhibitor,selective
- A2553 Fluvoxamine maleateSummary: Serotonin reuptake inhibitor,selective,antidepressant
- A1748 Ramelteon1 CitationTarget: Melatonin ReceptorsSummary: Agonist of melatonin receptor(M1-M2),highly selective
- A1987 Ki164254 CitationTarget: LPA ReceptorsSummary: LPA receptor antagonist