CAS: 106983-30-6; N-Octanoyl-Dl-Homoserine Lactone

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87206-01-7 106983-28-2 98426-48-3

上下游产品

α-amino-γ-butyrolactone hydrobromide n-°Ctanoic acid chloride

合成工艺路线路线简述

    📜α-氨基-γ-丁内酯氢溴酸盐,辛酰氯置于吡啶体系中,用 氯仿 用作溶剂,化学反应 16.0H,以67%的收率获得n-辛酰基-Dl-高丝氨酸内酯(2-8oc)
    参考文献:Synthesis And Biological Evaluation Of New N-Acyl-Homoserine-Lactone Analogues,Based On Triazole And Tetrazole Scaffolds,Acting As Luxr-Dependent Quorum Sensing Modulators
    标题:Synthesis And Biological Evaluation Of New N-Acyl-Homoserine-Lactone Analogues,Based On Triazole And Tetrazole Scaffolds,Acting As Luxr-Dependent Quorum Sensing Modulators
    摘要:New Analogues Of N-Acyl-Homoserine-Lactone (Ahl),In Which The Amide Was Replaced By A Triazole Or Tetrazole Ring,Were Prepared And Tested For Their Activity As Luxr-Dependent Qs Modulators. Several Compounds Showed A Level Of Antagonistic Or Agonistic Activity,Notably Some 1,4-Triazolic And 1,5-Tetrazolic Derivatives,Whereas The 2,5-Tetrazolic Compounds Were Inactive. In 1,5-Tetrazoles,Substituted With Butyrolactone And An Alkyl Chain,The Activity Was Reversed,Depending On The Connection Between The Lactone And The Tetrazole. The C-N Connected Compounds Were Agonists Whereas The C-C Connected Ones Were Antagonists. (C) 2012 Elsevier Ltd. All Rights Reserved.
    Doi:10.1016/j.Bmc.2012.06.007

    专利信息


    专利号:US-8222434-B1
    优先权日:2009-04-04
    标 题 :Bactobolin analog and synthesis method thereof
    发明人:GREENBERG E PETER; CHANDLER JOSEPHINE R; DUERKOP BRECK; LIMA PATRICIA SILVA; BLODGETT JOSHUA ALAN; CLARDY JON; SEYEDSAYAMDOST MOHAMMAD R
    权利人:GREENBERG E PETER; CHANDLER JOSEPHINE R; DUERKOP BRECK; LIMA PATRICIA SILVA; BLODGETT JOSHUA ALAN; CLARDY JON; SEYEDSAYAMDOST MOHAMMAD R; UNIV WASHINGTON CT COMMERCIALI; HARVARD COLLEGE
    摘要:The present inventions are directed to a novel bactobolin analog bactobolin D. The present inventions also are directed to a method of producing a composition comprising at least one bactobolin analog using a bacteria strain comprising a bacterial cell comprising the biosynthetic locus of the bactobolin analog in Burkholderia thailandensis (bta cluster) or a homolog structure (at least 95% sequence identity) thereof, and further isolation and purification of the bactobolin analog. For example, the bacterial strain can be a wild type bacterial strain such as a Burkholderia strain comprising a bta cluster (e.g. Burkholderia thailandensis (e.g. E264, Bt4, and TXDOH) and Burkholderia pseudomallei (e.g. K96243, 1106a, and 1106b).

    专利号:CN-115948483-A
    优先权日:2022-12-30
    标题:Method for enhancing synthesis of polyhydroxyalkanoate by bacteria based on quorum sensing signal molecules

    专利号:CN-115948483-B
    优先权日:2022-12-30
    标 题 :A method for enhancing bacterial synthesis of polyhydroxyalkanoates based on quorum sensing signaling molecules

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Li T, Et Al. Involvement Of Acylated Homoserine Lactones (Ahls) Of Aeromonas Sobria In Spoilage Of Refrigerated Turbot (Scophthalmus Maximus L.). Sensors (Basel). 2016 Jul 13;16(7):1083.
    [参考文献]: Benjamin Michael Davis, Et Al. The Interaction Of N-Acylhomoserine Lactone Quorum Sensing Signaling Molecules With Biological Membranes: Implications For Inter-Kingdom Signaling. Plos One. 2010 Oct 20;5(10):E13522.
    [参考文献]: Jitesh A Soares, Et Al. Detection Of Acyl-Homoserine Lactones By Escherichia And Salmonella. Curr Opin Microbiol. 2011 Apr;14(2):188-93.
    [参考文献]: Kay H Mcclean, Et Al. Quorum Sensing And Chromobacterium Violaceum: Exploitation Of Violacein Production And Inhibition For The Detection Of N-Acylhomoserine Lactones. Microbiology (Reading). 1997 Dec:143 ( Pt 12):3703-3711.
    [参考文献]: L Eberl, Et Al. N-Acyl Homoserinelactone-Mediated Gene Regulation In Gram-Negative Bacteria. Syst Appl Microbiol. 1999 Dec;22(4):493-506.

    合成参考文献


    参考文献:10.1007/s00203-017-1338-5
    摘要:Zhao K, Li W, Huang T, Song X, Zhang X, Yue B. Comparative transcriptome analysis of Trueperella pyogenes reveals a novel antimicrobial strategy. Arch Microbiol. 2017 Jul;199(5):649–55. doi: 10.1007/s00203-017-1338-5.
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