A-84543
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| 識別資訊 | |
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| CAS號 | 161416-43-9  [NIH] |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| 化學資訊 | |
| 化學式 | C11H16N2O |
| 摩爾質量 | 192.26 g·mol−1 |
| 3D模型（JSmol） | |
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A-84543是一種含氮有機化合物，分子式C11H16N2O，是美國雅培公司研發的菸鹼型乙醯膽鹼受體激動劑，能作為開發相關化合物的先導化合物。[1][2][3][4]
參考文獻
- ^ Abreo MA, Lin NH, Garvey DS, Gunn DE, Hettinger AM, Wasicak JT, et al. Novel 3-Pyridyl ethers with subnanomolar affinity for central neuronal nicotinic acetylcholine receptors. Journal of Medicinal Chemistry. February 1996, 39 (4): 817–25. PMID 8632405. doi:10.1021/jm9506884.
- ^ Lin NH, Gunn DE, Li Y, He Y, Bai H, Ryther KB, et al. Synthesis and structure-activity relationships of pyridine-modified analogs of 3-[2-((S)-pyrrolidinyl)methoxy]pyridine, A-84543, a potent nicotinic acetylcholine receptor agonist. Bioorganic & Medicinal Chemistry Letters. February 1998, 8 (3): 249–54. PMID 9871663. doi:10.1016/S0960-894X(98)00019-5.
- ^ Wei ZL, Xiao Y, Yuan H, Baydyuk M, Petukhov PA, Musachio JL, et al. Novel pyridyl ring C5 substituted analogues of epibatidine and 3-(1-methyl-2(S)-pyrrolidinylmethoxy)pyridine (A-84543) as highly selective agents for neuronal nicotinic acetylcholine receptors containing beta2 subunits. Journal of Medicinal Chemistry. March 2005, 48 (6): 1721–4. PMID 15771418. doi:10.1021/jm0492406.
- ^ Carreras J, Avenoza A, Busto JH, Peregrina JM. Synthesis of azabicyclo[2.2.n]alkane systems as analogues of 3-[1-methyl-2-(S)-pyrrolidinyl- methoxy]pyridine (A-84543). The Journal of Organic Chemistry. April 2007, 72 (8): 3112–5. PMID 17371077. doi:10.1021/jo0700732.