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Development of peptidic MERS-CoV entry inhibitors / 药学学报
Acta Pharmaceutica Sinica ; (12): 1513-1519, 2015.
Article in Chinese | WPRIM | ID: wpr-320049
ABSTRACT
In 2012, a new SARS-like coronavirus emerged in the Middle East, namely the Middle East respiratory syndrome coronavirus (MERS-CoV). It has caused outbreaks with high mortality. During infection of target cell, MERS-CoV S protein S1 subunit binds to the cellular receptor (DPP4), and its S2 subunit HR1 and HR2 regions intact with each other to form a stable six-helix bundle to mediate the fusion between virus and target cell membranes. Hence, blocking the process of six-helix bundle formation can effectively inhibit MERS-CoV entry into the target cells. This review focuses on the recent advance in the development of peptidic entry inhibitors targeting the MERS-CoV S2 subunit.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Antiviral Agents / Peptides / Pharmacology / Physiology / Drug Design / Coronavirus Infections / Dipeptidyl Peptidase 4 / Drug Therapy / Virus Internalization / Spike Glycoprotein, Coronavirus Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Antiviral Agents / Peptides / Pharmacology / Physiology / Drug Design / Coronavirus Infections / Dipeptidyl Peptidase 4 / Drug Therapy / Virus Internalization / Spike Glycoprotein, Coronavirus Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2015 Type: Article