CAS: 52712-76-2; Bunazosin Hydrochloride

该化合物是一种选择性的α1-成虫受体对抗物,主要用于治疗良性先发性高血压和高血压,其行动机制包括阻塞前列腺和血管中的α1-抗体受体,导致肌肉平稳放松,降低尿道抗药性,降低血压.该化合物表现出高度的受体选择性,最大限度地减少反应性心血管等副作用.其特点是快速吸收和可预测的药用植物,确保治疗效果一致.Bunazosin 氢氯化物存在于各种配方中,包括平板和持续释放制剂,在剂量疗法中提供了灵活性,其功效和耐受性使它成为管理...

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      参考文献:Masafuta,Kiesi;Utikava,Kiexiko;Kavabata,Yukehj;Kanai,Takeho;Sugimoto,+
      标题:Masafuta,Kiesi;Utikava,Kiexiko;Kavabata,Yukehj;Kanai,Takeho;Sugimoto,+

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      专利信息


      专利号:CN-1747485-A
      优先权日:2004-09-09
      标 题:Synthesis of ring of mobile communication terminal

      专利号:US-6884842-B2
      优先权日:1997-10-14
      标题:Molecular compounds having complementary surfaces to targets
      发明人:SOANE DAVID S; BARRY STEPHEN E; GOODWIN ANDREW; OFFORD DAVID A; PERROTT MICHAEL G
      权利人:ALNIS BIOSCIENCES INC
      摘要:Synthetic polymer complements (SPCs) are provided, as well as methods for their synthesis and use. The SPCs may have surfaces that include functional groups that are complementary to surface sites of targets such as nanostructures or macromolecular targets, and may be capable of specifically interacting with such targets. The positions of the functional groups in one embodiment are stabilized by a polymer network. The SPCs are formed by contacting the target with a set of monomers which self-assemble on the target, and then are polymerized into a network to form the synthetic polymer complement. At least a portion of the surface of the resulting SPC thus may include an imprint of the target. The complex of the SPC and the target may be the desired product. Alternatively, the target is released, for example, by controllably expanding and contracting the crosslinked network. The SPC is isolated and used in many applications.

      专利号:CN-206849343-U
      优先权日:2017-04-21
      标题 :A Demonstration Device of Force Synthesis and Decomposition

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      主要参考文献


      1: Goto W, Ichikawa M, Tanaka E, Hara H, Araie M. Bunazosin hydrochloride reduces glutamate-induced neurotoxicity in rat primary retinal cultures. Brain Res. 2004 Apr 2;1003(1-2):130-7. doi: 10.1016/j.brainres.2003.12.030. 13(1):73-80. doi: 10.1097/00061198-200402000-00014. 109(11):1569-74. doi: 10.1001/archopht.1991.01080110105046. 23(1):43-56. doi: 10.1111/j.1527-3466.2005.tb00156.x. 32(6):975-82. doi: 10.1097/00005344-199812000-00015. 36(10):1213-32. Japanese. 13(4):312-8. doi: 10.1097/00061198-200408000-00009. 14(3):217-28. doi: 10.1089/jop.1998.14.217. 45(11):1166-71. 19(1):63-73. doi: 10.1089/108076803762718123. 10(5):559-67. 146(3):877-80. doi: 10.1016/s0022-5347(17)37952-1. 19(1):35-8. 39(5):399-400. doi: 10.1111/j.2042-7158.1987.tb03407.x. 33(11):1921-41. Japanese. 50(5):443-448. doi: 10.1007/s10384-006-0351-z. 45(11):4041-8. doi: 10.1167/iovs.03-1395. 48(5):465-9. doi: 10.1007/s10384-004-0108-5. 11(5):330-4. doi: 10.1248/bpb1978.11.330. 30(2):163-8. doi: 10.1097/00005344-199708000-00003.

      合成参考文献


      参考文献:10.2165/00002512-199609030-00007
      摘要:Haria M, Spencer CM. Unoprostone (isopropyl unoprostone). Drugs Aging. 1996 Sep;9(3):213–8; discussion 219. doi: 10.2165/00002512-199609030-00007.
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