Identification of Metabolite Compounds from A Ethanol Extract of Caulerpa racemosa using LC-MS/MS with Inhibitory Activity of Interleukin-1β and Expression Inhibitory Nitric Oxide Synthase Enzyme; In Silico Virtual Screening

Ega Widya Prayogo, Irawati Sholikhah, Suciati, Wiwied Ekasari, Retno Widyowati

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Osteoarthritis (OA) is the prevailing kind of arthritis, impacting a substantial number of individuals globally. The incidence of OA is on the rise and is projected to further increase due to the aging population and escalating rates of obesity. This study aims to evaluate the anti-OA potential of Caulerpa racemosa. The Caulerpa racemosa 96 % ethanol extract of the plant was analysed using LC-MS/MS. The metabolite compositions were identified as polyunsaturated fatty acids, terpenes, bisindole alkaloids and diterpenoids. The 18 compounds analysed by LC-MS/MS, and the binding affinity of the compounds to the target proteins Interleukin-1 (PDB ID: 1ITB) was assessed by molecular docking fucosterol (∆G = –8.29 kcal/mol), variolin A (∆G = –8.02 kcal/mol), and clionasterol (∆G = –7.50 kcal/mol) and Nitric Oxide Synthase Inducible (3E7G) was assessed by molecular docking. Brassicasterol (∆G = –9.25 kcal/mol), fucosterol (∆G = –9.20 kcal/mol) and 24-methylenecholesterol (∆G = –9.04 kcal/mol) exhibited the highest docking scores, indicating their strong potential as inhibitors of IL1β and nitric oxide (NO). This knowledge is valuable for the future bioassay investigations about the possible applicability of these medicines as innovative solutions for OA.

Original languageEnglish
Article number8026
JournalTrends in Sciences
Volume21
Issue number9
DOIs
Publication statusPublished - Sept 2024

Keywords

  • Caulerpa racemosa
  • Inhibitor interleukin-1β
  • Inhibitory Nitric Oxide Synthase Enzyme
  • LC-MS/MS
  • Molecular docking
  • Osteoarthritis

Fingerprint

Dive into the research topics of 'Identification of Metabolite Compounds from A Ethanol Extract of Caulerpa racemosa using LC-MS/MS with Inhibitory Activity of Interleukin-1β and Expression Inhibitory Nitric Oxide Synthase Enzyme; In Silico Virtual Screening'. Together they form a unique fingerprint.

Cite this