CAS: 6036-25-5; Narbomycin

该化合物是一种自然产生的抗生素,属于被称为肛门素的化合物类别,通过发酵细菌菌株* 链球菌* 产生. 甲虫菌的化学结构具有复杂的双环核核心,这是抗生素抗生素的特征,并显示出一系列生物活动,特别是针对克伦阳性细菌. 甲虫菌已经研究其潜在的治疗用途,包括抑制细菌RNA聚合酶的能力,这对于细菌转录至关重要. 这一行动机制使得它成为了对抗生素发展,特别是抗生素抗抗生素抗药性方面进行进一步研究的候选体. 此外,甲虫素也显示出了某些抗肿瘤特性,表明其在癌症治疗中的潜在作用. 但是,与许多抗生素一样,其使用可能受到毒性和抗药性发展等因素的限制.

结构式图片

MSDS等安全信息

    上下游产品

    白丝菌素 Picromycin 19721-56-3
    Narbonolide 32885-75-9

    合成工艺路线路线简述

      📜白丝菌素置于potassium Dihydrogenphosphate,乙二胺四乙酸,还原型辅酶ii(Nadph)四钠盐体系中,化学反应生成 那波霉素
      参考文献:Macrolide Biosynthesis: A Single Cytochrome P450,Pick,Is Responsible For The Hydroxylations That Generate Methymycin,Neomethymycin,And Picromycin In Streptomyces Venezuelae
      标题:Macrolide Biosynthesis: A Single Cytochrome P450,Pick,Is Responsible For The Hydroxylations That Generate Methymycin,Neomethymycin,And Picromycin In Streptomyces Venezuelae
      摘要:The Final Step In The Biosynthesis Of Methymycin,Neomethymycin,And Picromycin Is An Hydroxylation,Shown To Be Carried Out By The Cytochrome P-450 Monooxygenase,Pick. Direct Comparison Of The Relative K(Cat)/k-M Values For The Two Substrates,Yc-17 And Narbomycin,Showed A Threefold Rate Preference Of Pick For Narbomycin. (C) 1998 Elsevier Science Ltd. All Rights Reserved.
      DOI:10.1016/s0960-894X(98)00553-8

      海关参考信息

      专利信息


      专利号:US-2004018598-A1
      优先权日:2000-05-30
      标题 :Bio-intermediates for use in the chemical synthesis of polyketides
      发明人:SANTI DANIEL; ASHLEY GARY; MYLES DAVID C
      摘要:The present invention relates to compounds made by a subset of modules from one or more polyketide synthase (“PKSâ€?) genes that are used as starting material in the chemical synthesis of novel molecules, particularly naturally occurring polyketides or derivatives thereof. The biologically derived intermediates (“bio-intermediatesâ€?) generally represent particularly difficult compounds to synthesize using traditional chemical approaches due to one or more stereocenters. In one aspect of the invention, an intermediate in the synthesis of epothilone is provided that feeds into the synthetic protocol of Danishefsky and co-workers. In another aspect of the invention, intermediates in the synthesis of discodermolide are provided that feed into the synthetic protocol of Smith and co-workers. By taking advantage of the inherent stereochemical specificity of biological processes, the syntheses of key intermediates and thus the overall syntheses of compounds like epothilone and discodermolide are greaty simplified.

      专利号:US-2002192767-A1
      优先权日:1999-10-13
      标题 :Biosynthesis of polyketide synthase substrates
      发明人:KHOSLA CHAITAN; PFEIFER BLAINE
      摘要:The use of enzymes which catalyze the production of starter and extender units for polyketides is described. In addition, modified loading modules are described, which can accept a variety of starting units such as substituted benzoates, and which can be used to generate substituted derivatives of natural products. These enzymes may be used to enhance the yield of polyketides that are natively produced or polyketides that are rationally designed. By using these techniques, the synthesis of a complete polyketide has been achieved in E. coli . Production can be enhanced in microbial organisms of polyketides and other secondary metabolites by delaying production until after exponential phase and by maintaining relatively constant nutrient levels in the medium. In addition, polyketide production can be enhanced by providing an expression system for a thioesterase II. Thus, by modifying the host organism and changing the culture conditions, synthesis of a secondary metabolite can be enhanced. The present invention also results in a host organism with desirable characteristics to be used in the production of such polyketides and to assess the results of gene shuffling.

      专利号:WO-02068613-A1
      优先权日:2001-02-28
      标题 :Biosynthesis of polyketide synthase substrates
      发明人:KHOSLA CHAITAN; PFEIFER BLAINE
      权利人:UNIV LELAND STANFORD JUNIOR; KHOSLA CHAITAN; PFEIFER BLAINE
      摘要:The use of enzymes which catalyze the production of starter and extender units for polyketides is described. In addition, modified loading modules are described, which can accept a variety of starting units such as substituted benzoates, and which can be used to generate substituted derivatives of natural products. These enzymes may be used to enhance the yield of polyketides that are natively produced or polyketides that are rationally designed. By using these techniques, the synthesis of a complete polyketide has been achieved in E. coli. Production can be enhanced in microbial organisms of polyketides and other secondary metabolites by delaying production until after exponential phase and by maintaining relatively constant nutrient levels in the medium. In addition, polyketide production can be enhanced by providing an expression system for a thioesterase II. Thus, by modifying the host organism and changing the culture conditions, synthesis of a secondary metabolite can be enhanced. The present invention also results in a host organism with desirable characteristics to be used in the production of such polyketides and to assess the results of gene shuffling.

      专利号:WO-2004075874-A1
      优先权日:2003-02-28
      标题 :Method for treatment and prevention of acute and chronic pseudomonas aeruginosa airway infections with inhalable macrolides
      发明人:MENEKSE OKTAY
      权利人:ANBICS PATENTS LICENCES AG; MENEKSE OKTAY
      摘要:Macrolides, in particular azalides such as azithromycin, are suited for the treatment or prevention of acute or chronic P. aeruginosa infections of the airways by inhala­tion. The mechanism of action is the inhibition of the quo­rum sensing of P. aeruginosa, in particular the impediment of the las and rhl quorum sensing systems synthesis and the impediment of the synthesis of the autoinducers N-[3-oxodo­1o decanoyl]-L-homoserine lactone and N-butyrylhomoserine lac­tone. This allows for inhalation treatments of P. aerugi-nosa infections at non-inhibiting concentrations of the macrolide.

      专利号:US-9382288-B2
      优先权日:2010-10-06
      标题 :Derivatives of steroid benzylamines, having an antiparasitic antibacterial, antimycotic and/or antiviral action
      发明人:BECKER KATJA; KRIEG REIMAR; SCHÖNECKER BRUNO
      权利人:BECKER KATJA; KRIEG REIMAR; SCHÖNECKER BRUNO; UNIV GIESSEN JUSTUS LIEBIG
      摘要:The present invention relates to compounds derived from steroids of the general formula (I) n nwherein L represents a linker and R # represents a steroid residue, the use of compounds of the general formula (I) in medicine and for the prophylaxis and/or the treatment of infectious diseases. Furthermore described are pharmaceutical compositions containing at least one compound of the general formula (I). A further aspect of the invention relates to the synthesis of said compounds of the general formula (I).

      专利号:US-2002045220-A1
      优先权日:1999-10-13
      标题:Biosynthesis of polyketide synthase substrates
      发明人:KHOSLA CHAITAN; PFEIFER BLAINE
      摘要:The use of enzymes which catalyze the production of starter and extender units for polyketides is described. In addition, modified loading modules are described, which can accept a variety of starting units such as substituted benzoates, and which can be used to generate substituted derivatives of natural products. These enzymes may be used to enhance the yield of polyketides that are natively produced or polyketides that are rationally designed. By using these techniques, the synthesis of a complete polyketide has been achieved in E. col. This achievement permits a host organism with desirable characteristics to be used in the production of such polyketides and to assess the results of gene shuffling.

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      合成参考文献


      摘要:Helvetica Chimica Acta., 38(935), 1955
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