CAS: 26048-05-5; (3S,6R,9S,12R,15S,18R)-3,9,15-Tribenzyl-6,12,18-Triisopropyl-4,10,16-Trimethyl-1,7,13-Trioxa-4,10,16-Triazacyclooctadecane-2,5,8,11,14,17-Hexaone

该化合物是一种由各种真菌物种,特别是波弗里雅和富森波氏基因组的真菌种生产的环六六二甲基乙酸甲酸酯,其独特的结构具有独特性,由交替的氨基酸和氢氧化酸残留物组成,形成循环安排;波弗里琴展示了一系列生物活动,包括细胞毒性和免疫抑制效应,使其对毒理学和药理学都感兴趣;已经证明它干扰了细胞过程,例如流行病和离子运输,特别是影响钾渠道;该化合物还因其具有生物杀菌潜力而引人注目,因为其具有抗菌特性;然而,它存在于食物和饲料产品中,引起对安全和管制限制的关切,因为它可能对人类和动物的健康造成危害;通常使用诸如液体色谱学和大规模光谱学等分析方法,来检测和量化各种基质素.

结构式图片

物理性质

上下游产品

(R)-2-Hydroxy-3-methylbutyric acid D-Val-OH benzyl (R)-2-hydroxy-3-methylbutanoate45H57N3O9*Na(1+)C45H57N3O9*Na(1+)

合成工艺路线路线简述

    📜D-缬氨酸置于盐酸,4-二甲氨基吡啶,1-氯-N,N,2-三甲基丙烯胺,硫酸,Palladium 10% On Activated Carbon,氢气,Caesium Carbonate,盐酸-N-乙基-N'-(3-二甲氨基丙基)碳二亚胺,N,N-二异丙基乙胺,Sodium Nitrite体系中,用 四氢呋喃,1,4-二氧六环,二氯甲烷,水,N,N-二甲基甲酰胺 用作溶剂,60.0 °C,689.49 Kpa 条件下,反应 67.5H,反应生成白僵菌素
    参考文献:流动化学合成天然和非天然环寡聚二肽
    标题:流动化学合成天然和非天然环寡聚二肽
    摘要:流动化学已成功地整合到一系列具有三种不同环尺寸的环寡聚二肽中,包括天然产物双曲霉素(1A),巴辛诺利德(2B)和烯属丙稀酸(1B).建立了可靠的流动化学方案,用于偶联和大环化以形成具有挑战性的n-甲基化酰胺.这种灵活的方法允许以高产率快速合成天然和非天然二肽肽,从而能够进一步探索其有前途的生物活性.
    Doi:10.1002/chem.201504457

    海关参考信息

    专利信息


    专利号:US-5662898-A
    优先权日:1990-08-20
    标 题 :Genes for the synthesis of antipathogenic substances
    发明人:LIGON JAMES M; HILL DWIGHT STEVEN; LAM STEPHEN TING; HAMMER PHILIP E
    权利人:CIBA GEIGY CORP
    摘要:The present invention is directed to the production of an antipathogenic substance (APS) in a host via recombinant expression of the polypeptides needed to biologically synthesize the APS. Genes encoding polypeptides necessary to produce particular antipathogenic substances are provided, along with methods for identifying and isolating genes needed to recombinantly biosynthesize any desired APS. The cloned genes may be transformed and expressed in a desired host organisms to produce the APS according to the invention for a variety of purposes, including protecting the host from a pathogen, developing the host as a biocontrol agent, and producing large, uniform amounts of the APS.

    专利号:US-9989489-B2
    优先权日:2006-12-14
    标 题 :Methods for calibrating an array of chemically-sensitive sensors
    发明人:ROTHBERG JONATHAN; HINZ WOLFGANG; JOHNSON Kim; BUSTILLO JAMES
    权利人:LIFE TECHNOLOGIES CORP; LIFE TECHNNOLOGIES CORP
    摘要:Methods and apparatus relating to very large scale FET arrays for analyte measurements. ChemFET (e.g., ISFET) arrays may be fabricated using conventional CMOS processing techniques based on improved FET pixel and array designs that increase measurement sensitivity and accuracy, and at the same time facilitate significantly small pixel sizes and dense arrays. Improved array control techniques provide for rapid data acquisition from large and dense arrays. Such arrays may be employed to detect a presence and/or concentration changes of various analyte types in a wide variety of chemical and/or biological processes. In one example, chemFET arrays facilitate DNA sequencing techniques based on monitoring changes in hydrogen ion concentration (pH), changes in other analyte concentration, and/or binding events associated with chemical processes relating to DNA synthesis.

    专利号:US-5817502-A
    优先权日:1994-06-08
    标题 :Genes for the synthesis of pyrrolnitrin

    专利号:US-11213031-B2
    优先权日:2017-11-13
    标 题:Tetrazolylpropyl derivatives and their use as fungicides
    发明人:SUDAU ALEXANDER; HOFFMANN SEBASTIAN; DAHMEN PETER; WEBSTER ROBERT ALAN; MEISSNER RUTH; GOERTZ ANDREAS; MILLER RICARDA; COQUERON PIERRE-YVES; BERNIER DAVID; NICOLAS LIONEL; BRUNET STEPHANE; KENNEL PHILIPPE; TOQUIN VALERIE; GOURGUES MATHIEU; LOQUE DOMINIQUE; THOMAS VINCENT
    权利人:BAYER AG; BAYER CROPSCIENCE AG
    摘要:The present invention relates to tetrazolylpropyl derivatives of formula (I) n nwherein one of V 1 and V 2 represents CR 3 and the other one of V 1 and V 2 represents N, Q represents a 6-membered aromatic cycle as defined in the specification, and R 1 , R 2 , R 3 , R 4 , and R 5 are defined as disclosed in the specification, to compositions comprising such compounds, to the use of said compounds as fungicides, as well as to particular intermediates useful in the synthesis of said tetrazolylpropyl derivatives.

    专利号:US-5639949-A
    优先权日:1990-08-20
    标 题 :Genes for the synthesis of antipathogenic substances

    专利号:WO-2016156284-A1
    优先权日:2015-04-02
    标 题 :Novel pyridine compounds for controlling phytopathogenic harmful fungi
    发明人:NISING CARL FRIEDRICH; BENTING JÜRGEN; DAHMEN PETER; WACHENDORFF-NEUMANN ULRIKE; MILLER RICARDA; COQUERON PIERRE-YVES; BERNIER DAVID; VORS JEAN-PIERRE; WITTROCK SVEN; KENNEL PHILIPPE; GENIX PIERRE; TSUCHIYA TOMOKI; NAUD SÉBASTIEN; MEISSNER RUTH
    权利人:BAYER CROPSCIENCE AG
    摘要:The present invention relates to a novel pyridine compound and its salts and N-oxides, a composition comprising such compound, a method for curatively or preventively controlling phytopathogenic harmful fungi of plants or crops comprising the step of applying such compound or composition, to the use of such compound or such composition to control phytopathogenic harmful fungi and to a seed that has been treated with such a compound or such a composition. Further the present invention relates to novel intermediate in the synthesis of the pyridine compounds of the invention.

    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

    主要参考文献


    1: Escrivá L, Jennen D, Caiment F, Manyes L. Transcriptomic Study of the Toxic Mechanism Triggered by Beauvericin in Jurkat Cells. Toxicol Lett. 2017 Dec 1. pii: S0378-4274(17)31496-0. doi: 10.1016/j.toxlet.2017.11.035. [Epub ahead of print] pii: E2058. doi: 10.3390/molecules22122058. doi: 10.1016/j.fm.2017.08.016. Epub 2017 Aug 30. doi: 10.1039/c7sc03093b. Epub 2017 Sep 25.
    5: Sun Y, Wink M, Wang P, Lu H, Zhao H, Liu H, Wang S, Sun Y, Liang Z. Biological characteristics, bioactive components and antineoplastic properties of sporoderm-broken spores from wild Cordyceps cicadae. Phytomedicine. 2017 Dec 1;36:217-228. doi: 10.1016/j.phymed.2017.10.004. Epub 2017 Oct 6. doi: 10.1016/j.fct.2017.11.019. [Epub ahead of print] Review. doi: 10.1371/journal.ppat.1006670. eCollection 2017 Oct.
    9: Tong Y, Liu M, Zhang Y, Liu X, Huang R, Song F, Dai H, Ren B, Sun N, Pei G, Bian J, Jia XM, Huang G, Zhou X, Li S, Zhang B, Fukuda T, Tomoda H, Ōmura S, Cannon RD, Calderone R, Zhang L. Beauvericin counteracted multi-drug resistant Candida albicans by blocking ABC transporters. Synth Syst Biotechnol. 2016 Oct 25;1(3):158-168. doi: 10.1016/j.synbio.2016.10.001. eCollection 2016 Sep.

    合成参考文献


    参考文献:10.1007/s00284-011-9977-2
    摘要:Valencia JW, Gaitán Bustamante AL, Jiménez AV, Grossi-de-Sá MF. Cytotoxic activity of fungal metabolites from the pathogenic fungus Beauveria bassiana: an intraspecific evaluation of beauvericin production. Curr Microbiol. 2011 Sep;63(3):306–12. doi: 10.1007/s00284-011-9977-2.
    参考文献:10.1094/phyto-01-11-0002
    摘要:Christ DS, Märländer B, Varrelmann M. Characterization and mycotoxigenic potential of Fusarium species in freshly harvested and stored sugar beet in Europe. Phytopathology. 2011 Nov;101(11):1330–7. doi: 10.1094/phyto-01-11-0002.
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