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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A3919 Vilazodone HydrochlorideSummary: Combined SSRI and 5-HT1A receptor partial agonist -
A3926 VortioxetineTarget: 5-HT1 Receptors|5-HT7 Receptors|5-HT3 Receptors|SERTSummary: 5-HT receptors antagonist -
A4632 Tetrahydropalmatine -
A4653 Pimavanserin hemitartrate -
A4654 Ketanserin tartrate -
A4655 Lumateperone tosylate -
A4656 Tandospirone citrate -
A4657 Jatrorrhizine chloride -
A4659 Vabicaserin hydrochloride -
A4711 Tetrahydro-β-carboline

