CAS: 11089-65-9; Tunicamycin

该化合物是抑制N-C-HexNAc酶的N-联锁性凝胶的核分子抗生素,阻塞酶UDP-HexNAc:多利肖尔磷酸酯HexNAc-1-磷酸酯转移酶.这一行动干扰了与脂质相关的寡头沙焦酸前体的形成,使其成为研究尿液细胞蛋白凝胶路径的宝贵工具.Tunicamycin被广泛用于引发内分泌性内聚体应力压力和蛋白反应的研究中,对细胞压力机制及吸附症提供了深入的了解.其特性和特性使得它特别有助于调查生物合成基因蛋白素,ER质量控制和相关代谢障碍.高纯度配方中可以使用,Tunicamycin确保可靠和可复制的实验结果.

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    专利号:US-6376475-B1
    优先权日:1997-05-30
    标 题 :Control of immune responses by modulating activity of glycosyltransferases
    发明人:MARTH JAMEY D; PAULSON JAMES C
    权利人:ABARON BIOSCIENCES INC; UNIV CALIFORNIA
    摘要:The invention provides methods for inhibiting immune responses by inhibiting the biosynthesis of the sialyl galactosides that are involved in immune responses. In particular, B lymphocyte-mediated immune responses are mediated by interfering with synthesis of α2,6 sialylgalactosides, while T lymphocyte-mediated immune responses are inhibited by blocking synthesis of α2,3 sialylgalactosides. The inhibition is accomplished by, for example, inhibiting the activity of a glycosyltransferase involved in synthesis of the respective sialyl galactoside.

    专利号:US-6083911-A
    优先权日:1998-12-10
    标题:Arenavirus receptor and methods of use
    发明人:CAMPBELL KEVIN P; HENRY MICHAEL; YAMADA HIROKI; WILLIAMSON ROGER; CAO WEI; OLDSTONE MICHAEL
    权利人:UNIV IOWA RES FOUND; SCRIPPS RESEARCH INST
    摘要:Disclosed is a method for inhibiting the binding of an arenavirus to a cellular receptor. The method involves providing, in soluble form, a reagent comprising α-dystroglycan or a portion thereof, the reagent being characterized by the ability to bind to the arenavirus thereby inhibiting the binding of the arenavirus to the cellular receptor. The reagent is contacted with an arenavirus particle prior to infection of a cell by the arenavirus particle. Also disclosed are methods for treating an arenavirus infection in a patient and preventing an arenavirus infection in an individual at risk. These methods involve providing a therapeutic composition comprising α-dystroglycan or a portion thereof which is characterized by the ability to bind to arenaviruses, thereby inhibiting the binding of arenaviruses to a cellular receptor; and administering the composition to the patient or individual at risk. Arenaviruses to which the methods of the present invention apply include, without limitation, Lymphocyte Choriomeningitis Virus, Lassa fever virus, Mobala, and Oliveros. In another aspect, the disclosure relates to an embryonic stem cell line, and cells derived therefrom, which is homozygous for a disrupted dystroglycan gene, wherein the disruption prevents the synthesis of functional dystroglycan in the cells. Applications of the dystroglycan null embryonic stem cells include producing dystroglycan or a portion thereof in the cells and also for identifying portions of dystroglycan necessary for arenavirus infection. Also disclosed is a method for identifying antiviral compounds which interfere specifically with the binding of arenavirus and α-dystroglycan, comprising providing a binding assay system for the determination of binding of arenavirus and α-dystroglycan. The candidate antiviral compounds are introduced into the binding assay system and antiviral compounds which substantially inhibit binding of arenavirus to α-dystroglycan are identified.

    专利号:US-8802380-B2
    优先权日:2007-06-04
    标 题 :Method for testing or screening protein synthesis inhibitors
    发明人:DREYFUSS GIDEON; KASIM MUMTAZ
    权利人:DREYFUSS GIDEON; KASIM MUMTAZ; UNIV PENNSYLVANIA
    摘要:This invention provides methods for screening an inhibitor of protein synthesis by measuring the level of relocalization of an SMN complex component from the cytoplasm to the nucleus. Additionally, the invention provides a kit and a system for screening protein synthesis inhibitors in a cell.

    专利号:US-6955886-B1
    优先权日:1998-05-15
    标题:Scintillation proximity assay for the detection of peptidoglycan synthesis
    发明人:DESOUSA SUNITA; PRAHLAD DWARAKANATH
    权利人:ASTRAZENECA AB
    摘要:The invention provides a scintillation proximity assay for detecting peptidoglycan synthesis. The assay is especially suitable for high throughput screening of compounds affecting peptidoglycan synthesis.

    专利号:US-2004116371-A1
    优先权日:2002-09-30
    标 题 :Methods for polysaccharide adhesion synthesis modulation
    发明人:ROMEO TONY; WANG XIN
    摘要:There is provided a method for modulation of polysaccharide adhesin synthesis involving products of the ycdSRQP gene operon in bacteria, depicted in SEQ. ID. NO. 1 and 2. Also provided is the use of an inhibitor of a product of the ycdSRQP operon in improving the response of a mammalian patient suffering from a bacterial infection.

    专利号:WO-9967419-A1
    优先权日:1998-06-25
    标题 :β(1,6)-GLUCAN SYNTHESIS AND CELL WALL ASSEMBLY ASSAY
    发明人:OSTROFF GARY R
    权利人:COLLABORATIVE GROUP LTD; OSTROFF GARY R
    摘要:Methods are disclosed for assessing an agent for an ability to inhibit β(1,6)-glucan synthesis and/or incorporation of β(1,6)-glucan into the cell wall, comprising contacting samples of yeast cells that are sensitive to a killer toxin that targets β(1,6)-glucan with a test agent and a lethal dose of the killer toxin, and/or contacting samples of yeast cells that are sensitive to the killer toxin with a test agent and a sublethal dose of the killer toxin, and assessing the permeability of the cells in the samples, such as by using a membrane-impermeable dye that fluoresces on contact with DNA.

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    主要参考文献


    1: Yamamoto K, Ichikawa S. Tunicamycin: chemical synthesis and biosynthesis. J Antibiot (Tokyo). 2019 Dec;72(12):924-933. doi: 10.1038/s41429-019-0200-1. Epub 2019 Jun 25. 37(1):272. doi: 10.1186/s13046-018-0935-8.
    3: Yoo J, Mashalidis EH, Kuk ACY, Yamamoto K, Kaeser B, Ichikawa S, Lee SY. GlcNAc-1-P-transferase-tunicamycin complex structure reveals basis for inhibition of N-glycosylation. Nat Struct Mol Biol. 2018 Mar;25(3):217-224. doi: 10.1038/s41594-018-0031-y. Epub 2018 Feb 19.
    4: Zhang X, Yuan Y, Jiang L, Zhang J, Gao J, Shen Z, Zheng Y, Deng T, Yan H, Li W, Hou WW, Lu J, Shen Y, Dai H, Hu WW, Zhang Z, Chen Z. Endoplasmic reticulum stress induced by tunicamycin and thapsigargin protects against transient ischemic brain injury: Involvement of PARK2-dependent mitophagy. Autophagy. 2014 Oct 1;10(10):1801-13. doi: 10.4161/auto.32136. Epub 2014 Aug 5.

    合成参考文献


    摘要:Australian Veterinary Journal., 76(287), 1998 []
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