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Covalent attachment of antagonists to the α7 nicotinic acetylcholine receptor: synthesis and reactivity of substituted maleimides

机译:拮抗剂与α7烟碱乙酰胆碱受体的共价结合:取代马来酰亚胺的合成和反应性

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摘要

The 3-methylmaleimide congeners of the natural product methyllycaconitine (MLA) and an analogue covalently attach to functional cysteine mutants of the α7 nicotinic acetylcholine receptor (nAChR).
机译:天然产物甲基可卡因碱(MLA)和类似物的3-甲基马来酰亚胺同类物与α7烟碱乙酰胆碱受体(nAChR)的功能性半胱氨酸突变体共价连接。

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  • 来源
    《Chemical Communications》 |2012年第53期|p.6699-6701|共3页
  • 作者单位

    Research School of Chemistry, Australian National University,Canberra, ACT 0200, Australia;

    Research School of Chemistry, Australian National University,Canberra, ACT 0200, Australia;

    Research School of Chemistry, Australian National University,Canberra, ACT 0200, Australia;

    Faculty of Pharmacy, The University of Sydney, Sydney,NSW 2006, Australia;

    NNF Centre for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2100 Copenhagen, Denmark;

    Department of Drug Design and Pharmacology,Faculty of Health and Medical Sciences, University of Copenhagen,Universitetsparken 2, 2100 Copenhagen, Denmark;

    Faculty of Pharmacy, The University of Sydney, Sydney,NSW 2006, Australia;

    Research School of Chemistry, Australian National University,Canberra, ACT 0200, Australia;

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  • 入库时间 2022-08-17 13:20:52

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