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Table · dataset · 2026

<b>Tomatidine Derivatives Suppress </b><b><i>Dengue Virus</i></b><b> Infection Through Entry and Post-Entry Inhibition</b>

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<p dir="ltr">Dengue is a rapidly spreading disease transmitted by mosquitoes and is caused by the <i>Dengue virus</i> (DENV), affecting approximately 390 million individuals globally.

Description

The only vaccine approved by the FDA, Dengvaxia, has limited effectiveness and is not authorized for use in India. Tomatidine, a steroidal alkaloid obtained from <i>Solanum</i> species, has demonstrated broad-spectrum antiviral properties, leading to the investigation of its derivatives for their anti-DENV activity.

In the current study, the anti-DENV potential of twelve such derivatives was assessed using a combination of <i>in vitro</i> and <i>in silico </i>approaches.<i> </i>this study, Vero CCL-81 cells were used to evaluate the cytotoxicity and antiviral effects of the derivatives in pre-, co-, and post-treatment settings. The results indicated that the derivatives 5c, 5d and 5f possessed the most potent antiviral effect. 5d achieved a 2.81 log decrease in viral RNA, while both 5f and 5c suppressed viral activity under both pre- and post-treatment conditions (5f has a selectivity index of 43.36), including the entry phase, as indicated by the entry assay.

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Furthermore, effective inhibition was noted between 0 and 9 h post-infection (hpi) and 15–21 hpi <i>via </i>time-of-addition assay, indicating dual-phase activity. Additionally, docking and molecular dynamics studies revealed stable interactions of compounds 5c and 5d with the non-structural proteins NS1 and NS5-RdRp of DENV, reinforcing the experimental observations. Furthermore, network pharmacology analysis predicted five major host proteins i.e. NFκB, MAPK11, HSP90AB1, TLR4 that might be targeted by the effective compounds.

In conclusion, tomatidine derivatives, especially 5d, 5f, and 5c, showed significant potential as anti-DENV therapeutics, necessitating additional mechanistic and <i>in vivo</i> studies to determine their clinical efficacy.</p>

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Inferred from text
Disease 75%
Provenance · 1 source records, 20 field assertions
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