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.
-   B7040 SNAP 5089Summary: α1A-adrenoceptor antagonist B7040 SNAP 5089Summary: α1A-adrenoceptor antagonist
-   B6572 GR 55562 dihydrochlorideSummary: 5-HT1B (5-HT1Dβ) silent antagonist B6572 GR 55562 dihydrochlorideSummary: 5-HT1B (5-HT1Dβ) silent antagonist
-   B7025 A 80426 mesylateSummary: α2-adrenoceptor antagonist and 5-HT uptake inhibitor B7025 A 80426 mesylateSummary: α2-adrenoceptor antagonist and 5-HT uptake inhibitor
-   B6558 CP 93129 dihydrochlorideSummary: 5-HT1B agonist, potent and highly selective B6558 CP 93129 dihydrochlorideSummary: 5-HT1B agonist, potent and highly selective
-   B6970 L-755,507Summary: β3 adrenergic receptor agonist B6970 L-755,507Summary: β3 adrenergic receptor agonist
-   B6548 RS 16566 dihydrochlorideSummary: ligand for the (R)-zacopride binding site B6548 RS 16566 dihydrochlorideSummary: ligand for the (R)-zacopride binding site
-   B6773 SDZ 21009Summary: β-adrenoceptor and 5-HT1A/1B receptor antagonist B6773 SDZ 21009Summary: β-adrenoceptor and 5-HT1A/1B receptor antagonist
-   B6545 N-DesmethylclozapineSummary: 5-HT2C serotonin receptor antagonist B6545 N-DesmethylclozapineSummary: 5-HT2C serotonin receptor antagonist
-   B6769 SR 59230A hydrochlorideSummary: A potent, selective β3 adrenoceptor antagonist B6769 SR 59230A hydrochlorideSummary: A potent, selective β3 adrenoceptor antagonist
-   B6540 Spiperone hydrochlorideSummary: 5-HT2A serotonin and selective D2-like dopamine receptor antagonist B6540 Spiperone hydrochlorideSummary: 5-HT2A serotonin and selective D2-like dopamine receptor antagonist
