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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C8724 (-)-Norepinephrine hydrochlorideSummary: An effective adrenergic receptor (AR) agonist, commonly used to induce cardiomyopathy animal models. -
C8725 Angiotensin II human acetateSummary: A vasoconstrictor and the main bioactive peptide of the renin/angiotensin system -
N2886 Kainic acid monohydrateSummary: Commonly used to establish neurodegenerative disease models -
C3816 PentoxifyllineSummary: A phosphodiesterase (PDE, especially PDE IV) inhibitor

