WB-4101
化合物
WB-4101，是一種化合物，可以作α1B-腎上腺素能受體的拮抗劑。1969年，WB-4101是首批為該受體開發的選擇性拮抗劑之一，常用於腎上腺素受體的研究，作爲開發更具選擇性藥物的先導化合物。[1][2][3][4][5][6]
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| CAS號 | 613-67-2  |
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| CompTox Dashboard (EPA) | |
| 化學資訊 | |
| 化學式 | C19H23NO5 |
| 摩爾質量 | 345.389 |
| 3D模型（JSmol） | |
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參見
參考文獻
- ^ The synthesis and pharmacological properties of a series of 2-substituted aminomethyl-1,4-benzodioxanes. Journal of Medicinal Chemistry. March 1969, 12 (2): 326–9. PMID 5791620. doi:10.1021/jm00302a033.
- ^ Characterization of alpha 1-adrenergic receptor subtypes in rat brain: a reevaluation of [3H]WB4104 and [3H]prazosin binding. Molecular Pharmacology. April 1986, 29 (4): 321–30. PMID 3010073.
- ^ Search for selective antagonists at alpha 1-adrenoreceptors: neutral or negative antagonism?. Farmaco. April 1998, 53 (4): 278–86. PMID 9658586. doi:10.1016/S0014-827X(98)00022-6.
- ^ Alpha 1-adrenoreceptor antagonists bearing a quinazoline or a benzodioxane moiety. Pharmaceutica Acta Helvetiae. March 2000, 74 (2–3): 181–90. PMID 10812956. doi:10.1016/S0031-6865(99)00049-7.
- ^ Affinity and activity profiling of unichiral 8-substituted 1,4-benzodioxane analogues of WB4101 reveals a potent and selective α1B-adrenoceptor antagonist. European Journal of Medicinal Chemistry. December 2012, 58: 184–91. PMID 23124215. doi:10.1016/j.ejmech.2012.09.049.
- ^ 6-methoxy-7-benzofuranoxy and 6-methoxy-7-indolyloxy analogues of 2-[2-(2,6-Dimethoxyphenoxy)ethyl]aminomethyl-1,4-benzodioxane (WB4101):1 discovery of a potent and selective α1D-adrenoceptor antagonist. Journal of Medicinal Chemistry. August 2013, 56 (16): 6402–12. PMID 23902232. doi:10.1021/jm400867d.