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.
- B1355 Cisatracurium BesylateTarget: AcetylcholineSummary: Neuromuscular-blocking drug
- B1364 ScopineSummary: α1-adrenergic receptor agonist
- B1344 Phenylephrine HClSummary: Selective α1-adrenergic receptor agonist
- B1326 DL-AdrenalineTarget: Androgen ReceptorsSummary: Adrenergic receptor agonist
- B1337 L-AdrenalineTarget: adrenergic receptorSummary: Adrenergic receptor agonist
- B1358 Epinephrine BitartrateTarget: adrenergic receptorSummary: Adrenergic receptor agonist
- B1333 Clonidine HClSummary: α2-adrenergic receptor agonist
- B3394 GuanfacineSummary: selective α2A receptor agonist
- B3395 AMD 3465Summary: CXCR4 antagonist,potent and selective
- B3397 AMD 3465 hexahydrobromideSummary: potent, selective CXCR4 antagonist