AI Article Synopsis

  • Dianthus superbus (DS) has significant medicinal potential, with extracts (ethyl acetate, butanol, distilled water) showing varying biological activities.
  • Ethyl acetate extracts exhibited strong anticancer effects against specific cancer cell lines, while butanol extracts showed potent antiviral activity against influenza A and B viruses.
  • Chemical analysis highlighted that flavonol glycosides are linked to anti-influenza activity, and cyclic peptides are associated with anticancer effects, suggesting DS could be effectively utilized in medicine and therapy.

Article Abstract

Dianthus superbus (DS) is a traditional medicinal herb well known for its medicinal and therapeutic potential and widely distributed in various Asian countries. The ethyl acetate (EA), butanol (Bu) and distilled water (DW) extracts of DS assessed for extraction of bioactive compounds and their biological activities. The chemical analysis was done using LC-MS/MS and antioxidant, anticancer and antiviral activities were determined. EA extracts showed strong anticancer activity with IC of 9.5, 13.8 and 69.9 μg/mL on SKOV, NCL-H1299 and Caski cancer cell lines, respectively. The Bu extracts exhibited strongest antiviral activity with respect to both influenza A and B viruses with IC values of 4.97 and 3.9 μg/mL, respectively. Also the metabolic profile for EA, Bu and DW extracts shows high variations and influence precisely the antioxidant, anticancer and antiviral properties. The quercetin 3- rutinoside and isorhamnetin 3- glucoside showed higher neuraminidase inhibition activity in dose dependent manner. Molecular docking study revealed that flavonol glycosides have higher binding activities towards influenza polymerase membrane glycoprotein. Correlation study showed that flavonol glycosides were linked to anti-influenza activity and cyclic peptides with anticancer activities. This study provides vital information for effective utilization of DS for medicinal, food and therapeutic purposes.

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Source
http://dx.doi.org/10.1016/j.fct.2019.01.013DOI Listing

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