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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A8953 MK 6096Summary: OX1/OX2 receptor antagonist -
B4783 Diphenidol HClSummary: antagonist of muscarinic M2 and M3 receptor -
B4784 Promethazine HClSummary: histamine H1 receptor antagonist -
B8200 SB 225002Summary: CXCR2 antagonist, potent and selective -
B4795 Labetalol HClSummary: A mixed α-/β-adrenergic antagonist -
B4876 K-Ras(G12C) inhibitor 121 CitationSummary: allosteric inhibitor of K-Ras(G12C) -
B4808 RG7090Summary: negative modulator of mGluR5 -
B4815 LCZ696Summary: A first in class ARNi (angiotensin receptor neprilysin inhibitor) -
B8031 MK-571 sodium salt hydrate3 CitationTarget: CysLT1Summary: CysLT1 receptor antagonist -
A8886 UNBS 5162Summary: A pan-antagonist of CXCL chemokines

