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Pharmacophores and biological activities of severe acute respiratory syndrome viral protease inhibitors

机译:严重急性呼吸系统综合症病毒蛋白酶抑制剂的药理作用和生物学活性

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摘要

Coronaviruses usually cause diseases with minor syndromes. However, an infectious disease caused by a novel human coronavirus induced severe acute respiratory syndrome (SARS). This disease first occurred in late 2002 and rapidly spread from its origin in southern China to > 25 countries during the 2003 epidemic. It affected ~ 8000 patients resulting in ~ 800 fatalities, a high mortality rate. To combat the disease, scientists have carried out cell-based assays to find the inhibitors on viral replication or focused on specific targets for developing their inhibitors as possible therapeutic agents. A promising target for SARS drug development is a chymotrypsin-like cysteine protease, a main protease responsible for the maturation of functional proteins in the life cycle of the SARS coronavirus. Several groups of inhibitors have been identified through high-throughput screening and rational drug design. The inhibitors reported in the literature and described in the patents are summarised in this review. These compounds may be useful to combat SARS if it reoccurs in the future and in developing new drugs for other coronaviruses with the main proteases.
机译:冠状病毒通常引起轻微综合症的疾病。但是,由新型人类冠状病毒引起的传染病可导致严重的急性呼吸道综合症(SARS)。该病最初发生于2002年底,在2003年的流行期间从其起源迅速扩散到中国南部到25个以上的国家。它影响了约8000名患者,导致约800人死亡,死亡率很高。为了对抗这种疾病,科学家们进行了基于细胞的分析,以发现病毒复制中的抑制剂,或者着眼于将其抑制剂开发为可能的治疗剂的特定靶标。 SARS药物开发的一个有希望的目标是一种胰凝乳蛋白酶样半胱氨酸蛋白酶,一种主要蛋白酶,负责SARS冠状病毒生命周期中功能蛋白的成熟。通过高通量筛选和合理的药物设计,已经鉴定出几类抑制剂。本文综述了文献中报道的抑制剂和专利中描述的抑制剂。如果将来再次出现SARS,这些化合物可能对防治SARS有用,并且可用于开发具有主要蛋白酶的其他冠状病毒的新药。

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