CAS: 113102-19-5; Rifamexil

该化合物是麻风素类的合成抗生素,主要用于抗菌特性,其特点是它能够抑制细菌RNA合成,将其与依赖DNA的RNA聚合酶酶结合,使其对一系列抗药性和某些克格朗阴性细菌有效.Rifamexil在治疗由Mycobactium结核病和其他菌种引起的感染方面的效力特别突出.该化合物一般具有良好的口服生物利用率,在肝脏中代谢,其药用动力受到各种因素的影响,包括剂量和病人特有的变量.与其他RNA酶一样,抗药性可以长期发展,需要仔细管理治疗疗法.此外,它可能与其他药物相互作用,因为其对肝酶的影响可以改变共同管理的药物的代谢.

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MSDS等安全信息

    上下游产品

    1,1-diethylthiourea 3-bromorifamycin S rifamycin P diethylamine

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      专利信息


      专利号:US-9693999-B2
      优先权日:2011-01-26
      标题:Small molecule RNase inhibitors and methods of use
      发明人:DUNMAN PAUL M; OLSON PATRICK D; CHILDERS WAYNE
      权利人:UNIV ROCHESTER; UNIV NEBRASKA; Temple University—Of the Commonwealth System of Higher Education
      摘要:Small molecule inhibitors of bacterial ribonuclease (e.g., RnpA) and methods for their synthesis and use are described herein. The methods of using the compounds include treating and preventing microbial infections and inhibiting bacterial ribonuclease. Also described herein are methods of identifying compounds for treating or preventing a microbial infection.

      专利号:WO-2009056955-A1
      优先权日:2007-10-30
      标题 :Amine-bearing phospholipids (abps), their synthesis and use
      发明人:ZUMBUEHL ANDREAS
      权利人:UNIV BASEL; ZUMBUEHL ANDREAS
      摘要:Disclosed herein are amine-bearing phospholipids (ABP). The ABPs display many properties and functionalities of naturally occurring phospholipids, but also new properties and functionalities, such as the ability to polymerize while maintaining structural integrity, that may supplement or expand the functionalities of naturally occurring phospholipids.

      专利号:US-9868747-B2
      优先权日:2014-02-18
      标题:Marinopyrrole derivatives and methods of making and using same
      发明人:LI RONGSHI; SEBTI SAID; LIU YAN; QIN YONG; SONG HAO; CHENG CHUNWEI
      权利人:H LEE MOFFITT CANCER CT & RES; CHONGQING ZEIN PHARMACEUTICAL CO LTD
      摘要:Marinopyrrole derivatives and methods for their synthesis and use are described herein. Novel cyclic and symmetric marinopyrroles with triazole substituents having antibacterial activity against resistant bacterial strains, such as MRSA are introduced. Also provided are methods of using the compounds for treating or preventing cancer and/or microbial infections.

      专利号:US-9907753-B2
      优先权日:2010-03-19
      标 题 :Lipid vesicle compositions and methods of use
      发明人:IRVINE DARRELL J; MOON JAEHYUN
      权利人:MASSACHUSETTS INST TECHNOLOGY
      摘要:The invention provides delivery systems comprised of stabilized multilamellar vesicles, as well as compositions, methods of synthesis, and methods of use thereof. The stabilized multilamellar vesicles may comprise prophylactic, therapeutic and/or diagnostic agents.

      专利号:US-2014315720-A1
      优先权日:2012-10-24
      标 题 :Polysaccharide ester microspheres and methods and articles relating thereto
      发明人:FALLON DENIS G; GARRETT THOMAS S; KIZER LAWTON E; ZAZZARA KAREN L; COMBS MICHAEL T; JOHNSON RICHARD K; DEHART GARY
      权利人:CELANESE ACETATE LLC
      摘要:A method for producing a polysaccharide ester microsphere may include forming a polysaccharide ester product from a polysaccharide synthesis, wherein the polysaccharide ester product comprises a polysaccharide ester and a solvent; diluting the polysaccharide ester product, thereby yielding a polysaccharide ester dope; and forming a plurality of polysaccharide ester microspheres from the polysaccharide ester dope. Suitable polysaccharides may include, but are not limited to, starch, cellulose, hemicellulose, algenates, chitosan, and any combination thereof. Esters thereof may be organic esters (e.g., acetate and the like), inorganic esters (e.g., sulfonates and the like), or combinations thereof. Further, the solids conent of the polysaccharide ester dope, in some instances, may be greater than about 16 wt %.

      专利号:US-6911318-B2
      优先权日:1999-03-03
      标 题:Bacterial transglycosylases: assays for monitoring the activity using Lipid II substrate analogs and methods for discovering new antibiotics
      发明人:KAHNE SUZANNE WALKER
      权利人:UNIV PRINCETON
      摘要:This invention provides a direct method for monitoring bacterial transglycosylase activity using labeled substrates produced by chemo-enzymatic synthesis wherein the labels are selected to permit the detection of both polymeric and non-polymeric products simultaneously, either directly or following the separation of product from starting material. The invention promotes the discovery of new antibiotics with activity against bacterial transglycosylases by a) laying the groundwork for structural analysis of purified, active transglycosylase (which permits structure-based design); and b) providing an assay that can be used to screen for inhibitors.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献


      1: Bacchi A, Mori G, Pelizzi G, Pelosi G, Nebuloni M, Panzone GB. Polymorphism-structure relationships of rifamexil, an antibiotic rifamycin derivative. Mol Pharmacol. 1995 Mar;47(3):611-23.

      合成参考文献


      参考文献:10.1023/a:1008070316079
      摘要:Bacchi A, Pelizzi G. Conformational variety for the ansa chain of rifamycins: Comparison of observed crystal structures and molecular dynamics simulations. Journal of Computer-Aided Molecular Design. 1999 Jul;13(4):385–96. doi: 10.1023/a:1008070316079.
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