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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B7038 JTE 013Summary: S1P receptor antagonist -
B7045 L-371,257Summary: human oxytocin (OT) receptor antagonist -
B7046 A-71623Summary: CCK1 agonist -
B7050 [Pyr1]-Apelin-13Summary: Endogenous ligand for apelin APJ receptor -
B7054 NNC 26-9100Summary: Somatostatin sst4 receptor agonist -
B7067 SDZ WAG 994Summary: A1 adenosine receptor agonist -
B7080 MRS 2693 trisodium saltSummary: P2Y6 agonist -
B7087 APC 366 (trifluoroacetate salt)Summary: mast cell tryptase inhibitor,selective and competitive -
B7088 L-161,982Target: Prostanoid ReceptorsSummary: EP4 receptor antagonist -
B7090 T 98475Summary: gonadotropin-releasing hormone (GnRH, LHRH) receptor antagonist,orally active

