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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B7027 CGH 2466 dihydrochlorideSummary: adenosine receptor antagonist -
B7032 EMD 386088 hydrochlorideSummary: 5-HT6 receptor agonist -
B7036 LY 320135Summary: CB1 receptor antagonist/inverse agonist -
B7040 SNAP 5089Summary: α1A-adrenoceptor antagonist -
B7041 MRS 2211Summary: P2Y13 receptor antagonist -
B7047 BIBO 3304 trifluoroacetateSummary: NPY Y1 receptor antagonist,highly selective -
B7057 (1R,1'S,3'R/1R,1'R,3'S)-L-054,264Summary: somatostatin sst2 receptor agonist -
B7069 IBC 293Summary: GPR109B (HM74) agonist -
B7073 JTE 907Summary: cannabinoid CB2 receptor inverse agonist -
B7074 (±)-AC 7954 hydrochlorideSummary: urotensin-II (UT) receptor agonist

