WB-4101

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]}

WB-4101

識別資訊
IUPAC命名法 2-(2,6-Dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane
CAS號	613-67-2  Y
PubChem CID	5685
IUPHAR/BPS	499
ChemSpider	5483
UNII	E9H51OIT2B
CompTox Dashboard（英語：CompTox Chemicals Dashboard） (EPA)	DTXSID1043885
化學資訊
化學式	C19H23NO5
摩爾質量	345.389
3D模型（JSmol（英語：JSmol））	交互式圖像
SMILES COc1cccc(c1OCCNCC2COc3ccccc3O2)OC
InChI InChI=1S/C19H23NO5/c1-21-17-8-5-9-18(22-2)19(17)23-11-10-20-12-14-13-24-15-6-3-4-7-16(15)25-14/h3-9,14,20H,10-13H2,1-2H3 Key:GYSZUJHYXCZAKI-UHFFFAOYSA-N

參見

• 苯二惡烷

參考文獻

1. 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.
2. 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.
3. 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.
4. 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.
5. 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. 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.