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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B7551 YIL 781Summary: Ghrelin receptor antagonist -
B7558 SR 58611A hydrochlorideSummary: β3-adrenergic receptor agonist -
B7561 NPEC-caged-serotoninSummary: 5-HT receptor agonist -
B7563 ZotepineSummary: 5-HT2A receptor and dopamine D2 receptor antagonist -
B7579 MJ 15Summary: CB1 receptor antagonist -
B7583 LY 266097 hydrochlorideSummary: 5-HT2B receptor antagonist -
B7605 MDL 100907Summary: 5-HT2A receptor antagonist -
B7606 AS 1269574Summary: GPR119 receptor agonist -
B7618 XCCSummary: Adenosine receptor antagonist -
B7625 GW 803430Summary: melanin-concentrating hormone receptor 1 (MCH1) antagonist

