CAS: 42189-56-0; 1-(Pyren-1-yl)-1H-Pyrrole-2,5-Dione

该化合物是一种有机化合物,其独特结构将阳性激素与一个发红素组结合在一起.该化合物一般会由于存在红色磷而表现出强烈的荧光效应,因此在各种应用中,包括在荧光标签和感应方面都有用.它经常用于生物协同反应,其中阳性物质组可以与含有硫醇的化合物发生反应,促进将青蒿素与蛋白或其他生物分子相连接.该化合物一般在有机溶剂中可以溶解,其光物理特性可能受到周围环境的影响,例如极性和粘性.此外,N-1-Pyrenyl)Mleimide可以作为分子相互作用和动态研究的探针,因为其进行能源转移过程的能力.在处理和储存时,应参考安全数据,以确保适当的实验室做法.

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CAS号42189-55-9 N-(1-Pyrenyl)ma... | CAS号1606-67-3 1-氨基芘

合成工艺路线路线简述

    📜N-(1-芘基)马来酰胺酸置于六甲基二硅氮烷,Zinc Dibromide体系中,用 苯 作为反应溶剂,化学反应 1.5H,以98%的收率获得产物n-(1-芘)-马来酰亚胺
    参考文献:Efficient Synthesis Of Fluorophore-Linked Maleimide Derivatives
    标题:Efficient Synthesis Of Fluorophore-Linked Maleimide Derivatives
    摘要:
    DOI:10.1055/s-1998-2097

    海关参考信息

    专利信息


    专利号:US-6451543-B1
    优先权日:1998-08-31
    标题:Lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides
    发明人:KOCHENDOERFER GERD G; HUNTER CHRISTIE L; KENT STEPHEN B H; BOTTI PAOLO
    权利人:GRYPHON SCIENCES
    摘要:The present invention relates to methods and compositions for lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides that are incorporated in a lipid matrix. The invention is exemplified in production of a prefolded membrane polypeptide embedded within a lipid matrix via stepwise chemoselective chemical ligation of unprotected peptide segments, where at least one peptide segment is embedded in a lipid matrix. Any chemoselective reaction chemistry amenable for ligation of unprotected peptide segments can be employed. Suitable lipid matrices include liposomes, micelles, cell membrane patches and optically isotropic cubic lipidic phase matrices. Prefolded synthetic and semi-synthetic membrane polypeptides synthesized according to the methods and compositions of the invention also permit site-specific incorporation of one or more detectable moieties, such as a chromophore, which can be conveniently introduced during synthesis. The methods and compositions of the invention have multiple uses. For example, they can be used to assay ligand binding to membrane polypeptides and domains comprising a receptor, and thus are extremely useful for structure/function studies, drug screening/selection/design, and diagnostics and the like, including high-throughput applications. The methods and compositions of the invention are particularly suited for FRET analyses of previously inaccessible membrane polypeptides.

    专利号:US-9470680-B2
    优先权日:2011-02-28
    标 题:Fluorescence-based approach to monitor release factor-catalyzed termination of protein synthesis
    发明人:GONZALEZ JR RUBEN L; STERNBERG SAMUEL H; PULUKKUNAT DILEEP K
    权利人:GONZALEZ JR RUBEN L; STERNBERG SAMUEL H; PULUKKUNAT DILEEP K; UNIV COLUMBIA
    摘要:Provided are probes comprising a class 1 release factor conjugated to a fluorescent label and methods of making the probes. Also provided are methods for detecting conformational changes in ribosomes and associated molecules, such as class 1 release factors. In addition, methods of identifying a compound for reducing nonsense-mediated decay of mRNA and/or for inhibiting termination of protein synthesis at a premature stop codon, are described. Methods of assaying RF3 activity are also included.

    专利号:US-7482425-B2
    优先权日:1999-08-26
    标题:Compositions for lipid matrix-assisted chemical ligation
    发明人:KOCHENDOERFER GERD G; HUNTER CHRISTIE L; KENT STEPHEN B H; BOTTI PAOLO
    权利人:AMYLIN PHARMACEUTICALS INC
    摘要:The present invention relates to methods and compositions for lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides that are incorporated in a lipid matrix. The invention is exemplified in production of a prefolded membrane polypeptide embedded within a lipid matrix via stepwise chemoselective chemical ligation of unprotected peptide segments, where at least one peptide segment is embedded in a lipid matrix. Any chemoselective reaction chemistry amenable for ligation of unprotected peptide segments can be employed. Suitable lipid matrices include liposomes, micelles, cell membrane patches and optically isotropic cubic lipidic phase matrices. Prefolded synthetic and semi-synthetic membrane polypeptides synthesized according to the methods and compositions of the invention also permit site-specific incorporation of one or more detectable moieties, such as a chromophore, which can be conveniently introduced during synthesis. The methods and compositions of the invention have multiple uses. For example, they can be used to assay ligand binding to membrane polypeptides and domains comprising a receptor, and thus are extremely useful for structure/function studies, drug screening/selection/design, and diagnostics and the like, including high-throughput applications. The methods and compositions of the invention are particularly suited for FRET analyses of previously inaccessible membrane polypeptides.

    专利号:US-2003018169-A1
    优先权日:1999-08-26
    标 题:Lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides

    专利号:EP-1107979-A2
    优先权日:1998-08-31
    标题:Lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides

    专利号:WO-0012536-A2
    优先权日:1998-08-31
    标 题 :Lipid matrix-assisted chemical ligation and synthesis of membrane polypeptides

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Curt B Boschek, Et Al. Disruption Of Interdomain Interactions Via Partial Calcium Occupancy Of Calmodulin. Biochemistry. 2007 Apr 17;46(15):4580-8.
    [参考文献]: E A Johnson, Et Al. Resonance Energy Transfer Between Tryptophan 57 In The Epsilon Subunit And Pyrene Maleimide Labeled Gamma Subunit Of The Chloroplast Atp Synthase. Biochemistry. 2001 Feb 13;40(6):1804-11.
    [参考文献]: M Yusof, Et Al. High Performance Liquid Chromatography Analysis Of D-Penicillamine By Derivatization With N-(1-Pyrenyl)Maleimide (Npm). Biomed Chromatogr. 2000 Dec;14(8):535-40.
    [参考文献]: Mauricio Baez, Et Al. Structural And Functional Roles Of Cys-238 And Cys-295 In Escherichia Coli Phosphofructokinase-2. Biochem J. 2003 Nov 15;376(Pt 1):277-83.
    [参考文献]: Mengmeng Wang, Et Al. Effects Of Ligand Binding And Oxidation On Hinge-Bending Motions In S-Adenosyl-L-Homocysteine Hydrolase. Biochemistry. 2006 Jun 27;45(25):7778-86.

    合成参考文献


    参考文献:10.1021/bi0523106
    摘要:Wang M, Unruh JR, Johnson CK, Kuczera K, Schowen RL, Borchardt RT. Effects of Ligand Binding and Oxidation on Hinge-Bending Motions in S-Adenosyl-l-homocysteine Hydrolase. Biochemistry. 2006 Jun 01;45(25):7778–86. doi: 10.1021/bi0523106.
    参考文献:10.1016/s0021-9258(18)66964-9
    摘要:Varga S, Mullner N, Pikula S, Papp S, Varga K, Martonosi A. Pressure effects on sarcoplasmic reticulum. Journal of Biological Chemistry. 1986 Oct;261(30):13943–56. doi: 10.1016/s0021-9258(18)66964-9.
    参考文献:10.1021/bi035424v
    摘要:Li J, Xiong Y, Bigelow DJ, Squier TC. Phospholamban binds in a compact and ordered conformation to the Ca-ATPase. Biochemistry. 2004 Jan 20;43(2):455–63. doi: 10.1021/bi035424v.
    参考文献:10.1074/jbc.274.46.32897
    摘要:Hammarström P, Persson M, Freskgârd PO, Mârtensson LG, Andersson D, Jonsson BH, Carlsson U. Structural mapping of an aggregation nucleation site in a molten globule intermediate. J Biol Chem. 1999 Nov 12;274(46):32897–903. doi: 10.1074/jbc.274.46.32897.
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