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.
-
B7178 L-748,337Summary: Competitive β3-adrenoceptor antagonist -
B7181 L-365,260Summary: cholecystokinin receptor 2 (CCK2) antagonist -
B7183 Nefazodone hydrochlorideSummary: 5-HT2A receptor antagonist -
B7184 Antalarmin hydrochlorideSummary: CRF1 antagonist -
B7185 CP 154526Summary: CRF1 receptor antagonist -
B7202 FPR A14Summary: Formyl peptide receptor (FPR) agonist -
B7216 Ro 04-6790Summary: 5-HT6 receptor antagonist -
B7226 Atipamezole hydrochlorideSummary: α2-adrenergic receptor antagonist -
B7232 DSP-4Summary: Adrenergic neurotoxin -
B7238 CCG 2046Summary: RGS4 inhibitor

