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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B5401 BIM 23042Summary: Antagonist of neuromedin B receptor,selective -
B5404 GLP-1 (9-36) amideSummary: antagonist at the human GLP-1 receptor -
B5408 AR-C 66096 tetrasodium saltSummary: P2Y12 antagonist,potent and selective -
B5412 CART (55-102) (rat)Summary: CART with potent appetite-suppressing activity -
B5413 CART (55-102) (human)Summary: CART with potent appetite-suppressing activity -
B5414 CART (62-76) (rat, human)Summary: inhibitor of food intake -
B5416 Cortistatin 14Summary: Endogenous neuropeptide that has structural and functional similarities to somatostatin-14 -
B5420 R 715Summary: bradykinin B1 receptor antagonist -
B5423 AmylinSummary: agonist for amylin, calcitonin, CGRP and adrenomedullin receptors -
B5424 AC 187Summary: Amylin receptor antagonist, Potent and selective

