Anti-Herpetic, Anti-Dengue and Antineoplastic Activities of Simple and Heterocycle-Fused Derivatives of Terpenyl-1,4-Naphthoquinone and 1,4-Anthraquinone
ABSTRACT: Quinones are secondary metabolites of higher plants associated with many biological activities, including antiviral effects and cytotoxicity. In this study, the anti-herpetic and anti-dengue evaluation of 27 terpenyl-1,4-naphthoquinone (NQ), 1,4-anthraquinone (AQ) and heterocycle-fused qui...
- Autores:
-
Roa Linares, Vicky Constanza
Tangarife Castaño, Verónica
Betancur Galvis, Liliana Amparo
Miranda Brand, Yaneth de Jesús
Ochoa Deossa, Rodrigo Alonso
Ángeles Castro, María
San Feliciano Martin, Arturo
García, Pablo
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2019
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/40305
- Acceso en línea:
- https://hdl.handle.net/10495/40305
- Palabra clave:
- Anthraquinones
Antraquinonas
Antiviral Agents
Antivirales
Chlorocebus aethiops
Dengue Virus
Virus del Dengue
Naphthoquinones
Naphthoquinones
HeLa Cells
Células HeLa
Herpesviridae
Herpesvirus 1, Human
Herpesvirus Humano 1
Herpesvirus 2, Human
Herpesvirus Humano 2
Vero Cells
Células Vero
https://id.nlm.nih.gov/mesh/D000880
https://id.nlm.nih.gov/mesh/D000998
https://id.nlm.nih.gov/mesh/D002522
https://id.nlm.nih.gov/mesh/D003716
https://id.nlm.nih.gov/mesh/D009285
https://id.nlm.nih.gov/mesh/D006367
https://id.nlm.nih.gov/mesh/D006564
https://id.nlm.nih.gov/mesh/D018259
https://id.nlm.nih.gov/mesh/D018258
https://id.nlm.nih.gov/mesh/D014709
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by/4.0/
| Summary: | ABSTRACT: Quinones are secondary metabolites of higher plants associated with many biological activities, including antiviral effects and cytotoxicity. In this study, the anti-herpetic and anti-dengue evaluation of 27 terpenyl-1,4-naphthoquinone (NQ), 1,4-anthraquinone (AQ) and heterocycle-fused quinone (HetQ) derivatives was done in vitro against Human Herpesvirus (HHV) type 1 and 2, and Dengue virus serotype 2 (DENV-2). The cytotoxicity on HeLa and Jurkat tumor cell lines was also tested. Using plaque forming unit assays, cell viability assays and molecular docking, we found that NQ 4 was the best antiviral compound, while AQ 11 was the most active and selective molecule on the tested tumor cells. NQ 4 showed a fair antiviral activity against Herpesviruses (EC50: <0.4 µg/mL, <1.28 µM) and DENV-2 (1.6 µg/mL, 5.1 µM) on pre-infective stages. Additionally, NQ 4 disrupted the viral attachment of HHV-1 to Vero cells (EC50: 0.12 µg/mL, 0.38 µM) with a very high selectivity index (SI = 1728). The in silico analysis predicted that this quinone could bind to the prefusion form of the E glycoprotein of DENV-2. These findings demonstrate that NQ 4 is a potent and highly selective antiviral compound, while suggesting its ability to prevent Herpes and Dengue infections. Additionally, AQ 11 can be considered of interest as a leader for the design of new anticancer agents. |
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