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Photodegradation and inhibition of drug-resistant influenza virus neuraminidase using anthraquinone-sialic acid hybrids

机译:蒽醌-唾液酸杂种的光降解和抗药性流感病毒神经氨酸酶的抑制

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摘要

The anthraquinone-sialic acid hybrids designed effectively degraded not only non-drug-resistant neuraminidase but also drug-resistant neuraminidase, which is an important target of anti-influenza therapy. Degradation was achieved using long-wavelength UV radiation in the absence of any additives and under neutral conditions. Moreover, the hybrids efficiently inhibited neuraminidase activities upon photo-irradiation.
机译:设计的蒽醌-唾液酸杂种不仅能有效降解非耐药性神经氨酸酶,而且还能有效降解耐药性神经氨酸酶,这是抗流感治疗的重要目标。在不存在任何添加剂的情况下,在中性条件下,使用长波紫外线辐射可实现降解。此外,杂种在光辐照下有效抑制神经氨酸酶活性。

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  • 来源
    《Chemical Communications》 |2013年第12期|1169-1171|共3页
  • 作者单位

    Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan;

    Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan;

    Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan;

    Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan;

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  • 入库时间 2022-08-17 13:17:57

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