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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B5396 Lys-BradykininSummary: Endogenous bradykinin receptor agonist -
B5397 [Lys5,MeLeu9,Nle10]-NKA(4-10)Summary: Highy selective and potent NK2 receptor agonist -
B5398 [Phe8Ψ(CH-NH)-Arg9]-BradykininSummary: Selective bradykinin B2 receptor agonist -
B5399 Sar-[D-Phe8]-des-Arg9-BradykininSummary: selective bradykinin B1 receptor agonist -
B5400 Ac9-25Summary: formyl peptide receptor 1 (FPR1) ligand -
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

