CAS: 6543-77-7; Doxycyline

该化合物是抗生素四环乙烷的一种半合成衍生物,专门用来加强其抗菌特性,其特点是对各种克型阳性细菌和克型阴性细菌的广谱活动,使其有效治疗各种感染;该化合物具有复杂的四环结构,对其行动机制至关重要,主要包括抑制细菌蛋白合成,将其与30-S核子核子元素结合. 4-环氧环球物质在酸性环境中具有稳定性,可以提高其生物利用率.此外,该物质表现出相对较低的毒性特征,适合治疗用途.然而,与其他四环球病一样,该物质可能会产生副作用,如胃肠扰动和光敏度等,其使用还受到抗生素抗药性开发潜力的限制.

结构式图片

MSDS等安全信息

    上下游产品

    CAS号564-25-0 强力霉素

    合成工艺路线路线简述

      📜强力霉素置于溶剂黄146体系中,化学反应 24.0H,以650 Mg的收率获得产物4-环氧氯丙烷强力霉素
      参考文献:Kertscher; Habermann; Pohle,Scientia Pharmaceutica,1998,Vol. 66,# 4,P. 287-296
      标题:Kertscher; Habermann; Pohle,Scientia Pharmaceutica,1998,Vol. 66,# 4,P. 287-296

      海关参考信息

      专利信息


      专利号:US-2021015837-A1
      优先权日:2020-04-08
      标题 :Method of Manufacturing an antiviral super treatment
      发明人:STAFFORD VIVI R
      权利人:STAFFORD VIVI R
      摘要:Method of Manufacturing an antiviral super pill or syrup for the treatment of viral infection such as SARS-CoV-2 (Covid 19). A cyclin antibiotic as well as a macrolide antibiotic are combined within the same compounded pill or capsule for the treatment of viruses. Doxycycline, a cyclin, binds to the 30S ribosomal subunit, and presumably to the 50S ribosomal subunit, thereby blocking the binding of aminoacyl-tRNA to the mRNA-ribosome complex, Azithromycin, a macrolide, reversibly binds to the 50S ribosomal subunit of the 70S ribosome of sensitive microorganisms, thereby inhibiting the translocation step of protein synthesis, wherein a newly synthesized peptidyl tRNA molecule moves from the acceptor site on the ribosome to the peptidyl (donor) site, and consequently inhibiting RNA-dependent protein synthesis leading to cell growth inhibition and cell death. As a result, this combination can provide immunity from certain viruses, such as Coronavirus 2019 (Covid 19) when given at the same time of a nasopharyngeal exposure to virus particles within numbers greater or less than 1000 virions, as a treatment regimen for a cure or as a prophylaxis for those exposed or were presumably exposed.

      专利号:WO-2004046348-A1
      优先权日:2002-11-17
      标题:Methods, nucleic acid constructs and cells for treating neurodegenerative disorders
      发明人:OFFEN DANIEL; MELAMED ELDAD; LEVY YOSEF
      权利人:UNIV RAMOT; OFFEN DANIEL; MELAMED ELDAD; LEVY YOSEF
      摘要:A method of treating a neurodegenerative disorder is provided. The method is effected by administering to an individual in need thereof cells capable of exogenously regulatable neurotransmitter synthesis thereby treating the neurodegenerative disorder.

      专利号:US-2013236964-A1
      优先权日:2002-11-17
      标 题:Methods, nucleic acid constructs and cells for treating neurodegenerative disorders
      发明人:MELAMED ELDAD; OFFEN DANIEL; LEVY YOSEF; GREEN PNINA
      权利人:UNIV RAMOT
      摘要:A method of treating a neurodegenerative disorder is provided. The method is effected by administering to an individual in need thereof cells capable of exogenously regulatable neurotransmitter synthesis thereby treating the neurodegenerative disorder.

      供应商参考报价(招募中)

      品牌试剂参考报价(招募中)

      📌 第三方产品分析报告

      ✅ COA系统入驻 | 共享模式

      合成参考文献

      参考DOI号:10.1021/ja01498a037
      📝 需求与反馈
      尽可能描述清楚需求与问题信息
      ×

      通知