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首页> 外文期刊>Journal of Drug Delivery and Therapeutics >Repurposable Drug Candidates are Potential Therapeutic Target against Global SARS-CoV-2 Crisis
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Repurposable Drug Candidates are Potential Therapeutic Target against Global SARS-CoV-2 Crisis

机译:可重复的药物候选人是针对全球SARS-COV-2危机的潜在治疗目标

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This review provides a pharmacological approach to combat Severe Acute Respiratory Syndrome Corona Virus-2 (SARS-CoV-2) based on two comprehensive denominations which could be specifically intended for viral replication process by either inhibiting essential genomic viral enzymes or preventing viral entry to human cells. These denominations focused on immune therapies either to improve innate antiviral immune responses or to reduce impairment triggered by underactive inflammatory reactions. A variety of drug candidates are available which can inhibit SARS-CoV-2 infection and replication, comprising serine protease inhibitors: Transmembrane Orotease/Serine Subfamily member 2 (TMPRSS2), camostat mesylate, nafamostat mesylate, and angiotensin-converting enzyme inhibitors. This review is also concerned with identifying drugs and ongoing clinical trials with their mechanisms of action against SARS-CoV-2. Chloroquine and hydroxychloroquine, monoclonal antibody, off-label antiviral drugs, nucleotide analog remdesivir and broad-spectrum antiviral drugs also could be used as inhibitors of SARS-CoV-2. Moreover, non-steroidal anti-inflammatory drugs (NSAIDs), dexamethasone, and antiviral phytochemicals that are currently reachable, can prevent SARS-CoV-2 pandemic morbidity and mortality.
机译:本综述提供了一种药理学方法,可以基于两种综合面额来打击严重急性呼吸综合征Corona病毒-2(SARS-COV-2),这可能是通过抑制基本组织病毒酶或预防人类的病毒进入病毒复制过程细胞。这些指定的重点是免疫疗法,以改善先天抗病毒免疫应答或减少因不良炎症反应引发的损伤。可提供各种药物候选者,其可抑制SARS-COV-2感染和复制,包括丝氨酸蛋白酶抑制剂:跨膜OROTEASE /丝氨酸亚家族成员2(TMPRSS2),CAMOSTAT甲磺酸盐,NaFamostat甲磺酸盐和血管紧张素转换酶抑制剂。该审查还涉及鉴定药物和正在进行的临床试验,并采取对SARS-COV-2的行动机制。氯喹和羟基喹啉,单克隆抗体,非标签抗病毒药物,核苷酸类似物雷德肽和广谱抗病毒药也可用作SARS-COV-2的抑制剂。此外,目前可达的非甾体类抗炎药(NSAIDs),地塞米松和抗病毒植物化学,可以预防SARS-COV-2大流行病和死亡率。

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