首页> 外文期刊>Journal of Medicinal Chemistry >New Steroidal 4-Aminoquinolines Antagonize Botulinum Neurotoxin Serotype A in Mouse Embryonic Stem Cell Derived Motor Neurons in Postintoxication Model
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New Steroidal 4-Aminoquinolines Antagonize Botulinum Neurotoxin Serotype A in Mouse Embryonic Stem Cell Derived Motor Neurons in Postintoxication Model

机译:新的甾体4-氨基喹啉拮抗肉毒杆菌神经毒素血清蛋白质衍生神经元在晚期毒品模型中的血清型A

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摘要

The synthesis and inhibitory potencies against botulinum neurotoxin serotype A light chain (BoNT/A LC) using in vitro HPLC based enzymatic assay for various steroidal, benzothiophene, thiophene, and adamantane 4-aminoquinoline derivatives are described. In addition, the compounds were evaluated for the activity against BoNT/A holotoxin in mouse embryonic stem cell derived motor neurons. Steroidal derivative 16 showed remarkable protection (up to 89% of uncleaved SNAP-25) even when administered 30 min postintoxication. This appears to be the first example of LC inhibitors antagonizing BoNT intoxication in mouse embryonic stem cell derived motor neurons (mES-MNs) in a postexposure model. Oral administration of 16 was well tolerated in the mouse up to 600 mg/kg, q.d. Although adequate unbound drug levels were not achieved at this dose, the favorable in vitro ADMET results strongly support further work in this series.
机译:描述了对肉毒杆菌神经毒素的合成和抑制性疗效使用用于各种甾体,苯并噻吩,噻吩和金刚烷4-氨基喹啉衍生物的体外HPLC基酶测定的轻链(Bont / A LC)。 此外,在小鼠胚胎干细胞衍生的运动神经元中评估该化合物的对抗逆/溶质毒素的活性。 即使在30分钟的介质涂膜中,甾体衍生物16表现出显着的保护(高达89%的未切割的SNAP-25)。 这似乎是LC抑制剂在后曝光模型中拮抗小鼠胚胎干细胞衍生的电动元素(MES-MNS)中的局部诱导中毒的第一例。 口服施用16位在小鼠中耐受良好,高达600mg / kg,Q.D。 虽然此剂量未实现足够的未结合药物水平,但有利的体外探险结果在本系列中强烈支持进一步的工作。

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  • 来源
    《Journal of Medicinal Chemistry》 |2018年第4期|共14页
  • 作者单位

    Univ Belgrade Fac Chem Studentski Trg 16 POB 51 Belgrade 11158 Serbia;

    NCI Mouse Canc Genet Program Ctr Canc Res Frederick MD 21702 USA;

    US Army Med Res Inst Infect Dis Mol &

    Translat Sci Div 1425 Porter St Frederick MD 21702 USA;

    US Army Med Res Inst Infect Dis Mol &

    Translat Sci Div 1425 Porter St Frederick MD 21702 USA;

    Fac Chem Innovat Ctr Studentski Trg 12-16 Belgrade 11158 Serbia;

    US Army Med Res Inst Infect Dis Mol &

    Translat Sci Div 1425 Porter St Frederick MD 21702 USA;

    Univ Belgrade Inst Chem Technol &

    Met Njegoseva 12 Belgrade 11000 Serbia;

    Univ Belgrade Fac Chem Studentski Trg 16 POB 51 Belgrade 11158 Serbia;

    Univ Belgrade Fac Chem Studentski Trg 16 POB 51 Belgrade 11158 Serbia;

    US Army Med Res Inst Infect Dis Mol &

    Translat Sci Div 1425 Porter St Frederick MD 21702 USA;

    US Army Med Res Inst Infect Dis 1425 Porter St Frederick MD 21702 USA;

    Univ Belgrade Fac Chem Studentski Trg 16 POB 51 Belgrade 11158 Serbia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

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