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.
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B6842 R-96544 hydrochlorideSummary: 5-HT2 receptor antagonist -
B6848 Acifran1 CitationSummary: HM74A/GPR109A and GPR109B agonist,hypolipidemic agent -
B6855 NNC 63-0532Summary: NOP receptor agonist -
B6858 Zacopride hydrochlorideSummary: 5-HT3 receptor antagonist and 5-HT4 receptor agonist -
B6859 WAY 161503 hydrochlorideSummary: 5-HT2C receptor agonist -
B6860 SR 2640 hydrochlorideSummary: leukotriene D4 and E4 receptor antagonist -
B6863 Altanserin hydrochlorideSummary: 5-HT2A receptor antagonist -
B6867 PalmitoylisopropylamideSummary: FAAH inhibitor -
B6875 EMD 66684Summary: angiotensin AT1 receptor antagonist -
B6878 Ro 60-0175 fumarateSummary: 5-HT2 receptor agonist
