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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B1748 Esmolol HClSummary: Adrenergic receptor antagonist -
B1750 EthamsylateSummary: Haemostatic drug -
B1757 FlopropioneSummary: 5-HT receptor antagonist -
B1335 Guanabenz AcetateSummary: α2-adrenergic receptor agonist -
B1428 GW842166XTarget: cannabinoid receptorSummary: Cannabinoid receptor agonist -
B1369 Indacaterol MaleateSummary: Ultra-long-acting β-adrenoceptor agonist -
B1591 Ki16198Target: LPA ReceptorsSummary: LPA antagonist -
B1778 Levobetaxolol HClSummary: Adrenergic receptor antagonist -
B1783 Loxapine SuccinateSummary: Dopamine receptor antagonist -
B2250 LY310762Summary: 5-HT1D receptor antagonist

