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Progress of research on immune escape mechanism of coronavirus 冠状病毒免疫逃逸机制的研究进展
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2021-01-01 DOI: 10.11665/j.issn.1000-5048.20210101
R. Wang, Z. Zheng, Y. Zhang, R. Min, Y. Zhu, P. Zhang
Coronavirus is an important pathogen of humans and animals.Among them, the novel coronavirus disease (COVID-19) breaking out in 2019 has brought a fatal threat to human health.The host's innate immune response is the host's first line of defense against pathogen invasion, but an excessive immune response can also aggravate viral infection and pathological damage.The immune escape of coronavirus is a critical pathogenic mechanism causing death.This work mainly reviews the pathogenic mechanism of coronavirus immune escape from several aspects such as host immunosensor, interferon, cytokine and coronavirus antagonizing host immune response, which provide a theoretical reference for the development of anti-coronavirus drugs.
冠状病毒是人类和动物的重要病原体。其中,2019年爆发的新型冠状病毒病(COVID-19)给人类健康带来了致命威胁。宿主的先天免疫反应是宿主抵御病原体侵袭的第一道防线,但过度的免疫反应也会加重病毒感染和病理损伤。冠状病毒的免疫逃逸是导致死亡的重要致病机制。本文主要从宿主免疫传感器、干扰素、细胞因子、冠状病毒拮抗宿主免疫应答等几个方面综述冠状病毒免疫逃逸的致病机制,为抗冠状病毒药物的开发提供理论参考。
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引用次数: 0
Intervention effects of the extract of alismatis rhizoma on streptozotocin-induced type 2 diabetic rats 泽泻提取物对链脲佐菌素诱导的2型糖尿病大鼠的干预作用
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2017-10-01 DOI: 10.11665/J.ISSN.1000-5048.20170516
Lan-Jie Cao, K. Zhu, Cuihua Jiang, J. Gunn, C. Che, Jian Zhang, Zhiqi Yin
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引用次数: 1
Synthesis of aliskiren aliskiren的合成
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2011-01-01 DOI: 10.1055/s-0034-1380902
Wu Xiaoming
This paper describes a practical process for the preparation of aliskiren.Chiral building blocks 1 and 2 were prepared by chemical resolution,and a following five-step convergent synthesis led to aliskiren with an overall yield of 15.6%.The intermediates and the target compound were characterized by melting points,NMR and MS.The convergent synthetic process of aliskiren highlights reasonable yields,ease of operation,high stereoselectivity as well as only one chromatographic purification,and thus should be amenable to large-scale production.
本文介绍了一种制备阿利斯基仑的实用工艺。通过化学拆分制备手性构建块1和2,经过5步会聚合成得到aliskiren,总收率为15.6%。通过熔点、核磁共振和质谱对中间体和目标化合物进行了表征。聚类合成工艺产率合理,操作简便,立体选择性高,且只需一次色谱纯化,适合大规模生产。
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引用次数: 0
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中国药科大学学报
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