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Related Concept Videos

Arboviral Encephalitis01:25

Arboviral Encephalitis

Arboviral encephalitis refers to brain inflammation caused by arthropod-borne viruses, particularly those transmitted through mosquito vectors. Among these, West Nile virus (WNV), a member of the Flaviviridae family, is a significant public health concern. WNV is an enveloped, positive-sense, single-stranded RNA virus. Human infection typically begins when an infected mosquito introduces the virus into the dermis during feeding. The primary transmission cycle involves birds as amplifying hosts...
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Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
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Viral replication and dissemination rely on efficient mechanisms for host cell entry, genome replication, assembly, and release. Influenza viruses, such as types A and B, are negative-sense single-stranded RNA viruses with a segmented genome, that depend on two critical surface glycoproteins to carry out these processes: hemagglutinin (HA) and neuraminidase (NA). HA initiates infection by binding to sialic acid residues on the surface of host epithelial cells, facilitating receptor-mediated...
Antiviral Nucleoside Inhibitors01:22

Antiviral Nucleoside Inhibitors

Antiviral Nucleoside InhibitorsAntiviral nucleoside inhibitors are structural analogs of natural nucleosides that interfere with viral DNA or RNA synthesis. These compounds selectively target viral polymerases due to their resemblance to host nucleosides, thereby disrupting viral genome replication.Mechanism of Acyclovir ActionAcyclovir is a guanosine analog with a three-carbon acyclic side chain. It selectively targets herpes simplex virus type 1 (HSV-1), herpes simplex virus type 2 (HSV-2),...
Inhibitors of Virion Maturation and Assembly01:19

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Related Experiment Video

Updated: Jul 15, 2026

Zika Virus Infectious Cell Culture System and the In Vitro Prophylactic Effect of Interferons
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Zika Virus Infectious Cell Culture System and the In Vitro Prophylactic Effect of Interferons

Published on: August 23, 2016

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Zika virus entry inhibitors.

Weiyi Yin1, Rui Zhou2, Wencui Zhang1

  • 1Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

Bioorganic & Medicinal Chemistry
|March 7, 2026
PubMed
Summary

This review highlights Zika virus (ZIKV) entry inhibitors, focusing on small molecules that target host-virus interactions. It aims to advance ZIKV therapeutics by exploring diverse chemotypes and their potential in antiviral therapy.

Keywords:
Carbohydrate receptorDengue virusStructure-activity relationshipVirus entry inhibitorsZika virus

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Area of Science:

  • Virology
  • Drug Discovery
  • Infectious Diseases

Background:

  • Viral entry is crucial for infection, involving complex host-virus interactions.
  • Developing inhibitors targeting viral entry, particularly for viruses like Zika virus (ZIKV), lags behind replication inhibitors.
  • ZIKV, a neglected flavivirus, currently lacks effective therapeutic options.

Purpose of the Study:

  • To review the research progress of viral entry inhibitors for Zika virus (ZIKV).
  • To categorize ZIKV entry inhibitors based on the three major stages of the viral entry process.
  • To explore diverse chemotypes of small molecular entry inhibitors and their therapeutic potential.

Main Methods:

  • Classified review of ZIKV entry inhibitors based on the viral entry stages.
  • Inclusion of inhibitors acting on virus entry via time-of-addition experiments.
  • Overview of diverse small molecular chemotypes targeting viral entry.

Main Results:

  • Identified diverse chemotypes of small molecular entry inhibitors for ZIKV.
  • Highlighted inhibitors acting on virus entry, including those with preliminary mechanism characterization.
  • Presented a structured review of inhibitors targeting the three major stages of viral entry.

Conclusions:

  • Viral entry inhibitors represent a promising therapeutic strategy for ZIKV and other enveloped RNA viruses.
  • Further research into ZIKV entry inhibitors can lead to effective antiviral therapies.
  • This review aims to stimulate interest in ZIKV research and the potential of entry inhibitors.