Back to results
Bibliographic record · Consultation and access
Artículo

Unveiling tetrahydroquinolines as promising BVDV entry inhibitors: Targeting the envelope protein

Leal, Emilse Soledad et al · Academic Press Inc Elsevier Science · 2024

Open-access full text
Quick overview. Review the resource’s basic details, then access the content using the main button. This page shows only the information needed to identify, cite, and open the work.

Resource access

Open the content from the main option or choose another available source.

CONICET Digital CONICET Digital OAI-PMH
Entrar por CONICET Digital
Main access

Open-access full text

Texto completo identificado como acceso abierto.
Open text

Summary

Descripción general del contenido del recurso.

Bovine viral diarrhea virus (BVDV) is known to cause financial losses and decreased productivity in the cattle industry worldwide. Currently, there are no available antiviral treatments for effectively controlling BVDV infections in laboratories or farms. The BVDV envelope protein (E2) mediates receptor recognition on the cell surface and is required for fusion of virus and cell membranes after the endocytic uptake of the virus during the entry process. Therefore, E2 is an attractive target for the development of antiviral strategies. To identify BVDV antivirals targeting E2 function, we defined a binding site in silico located in domain IIIc at the interface between monomers in the disulfide linked dimer of E2. Employing a de novo design methodology to identify compounds with the potential to inhibit the E2 function, compound 9 emerged as a promising candidate with remarkable antiviral activity and minimal toxicity. In line with targeting of E2 function, compound 9 was found to block the virus entry into host cells. Furthermore, we demonstrated that compound 9 selectively binds to recombinant E2 in vitro. Molecular dynamics simulations (MD) allowed describing a possible interaction pattern between compound 9 and E2 and indicated that the S enantiomer of compound 9 may be responsible for the antiviral activity. Future research endeavors will focus on synthesizing enantiomerically pure compounds to further support these findings. These results highlight the usefulness of de novo design strategies to identify a novel class of BVDV inhibitors that block E2 function inhibiting virus entry into the host cell. Fil: Leal, Emilse Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Pascual, María José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentina

How to cite

Elegí el formato que necesitás y copiá la referencia al portapapeles.

APA 7

Leal, E. S. E. A. (2024). Unveiling tetrahydroquinolines as promising BVDV entry inhibitors: Targeting the envelope protein. http://hdl.handle.net/11336/267118

MLA

Leal, Emilse Soledad et al. "Unveiling tetrahydroquinolines as promising BVDV entry inhibitors: Targeting the envelope protein." 2024. http://hdl.handle.net/11336/267118.

Chicago

Leal, Emilse Soledad et al. 2024. "Unveiling tetrahydroquinolines as promising BVDV entry inhibitors: Targeting the envelope protein.". http://hdl.handle.net/11336/267118.

Harvard

Leal, E. S. E. A. 2024, Unveiling tetrahydroquinolines as promising BVDV entry inhibitors: Targeting the envelope protein, Academic Press Inc Elsevier Science, available at: http://hdl.handle.net/11336/267118 [Accessed 8 Aug. 2026].

Share and print

Save the record, copy its permanent link, or print it as a PDF.

Export reference

You can export the record in common formats for use in a reference manager.

Resource details

Bibliographic information to help confirm that this is the correct material.

Title
Unveiling tetrahydroquinolines as promising BVDV entry inhibitors: Targeting the envelope protein
Author / contributors
Leal, Emilse Soledad et al
Publisher
Academic Press Inc Elsevier Science
Publication year
2024
ISSN
0042-6822
ISSN
0042-6822
Language
English

Subjects

Explore related resources through these subjects.

Copied