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Phytochemical Screening, In Vitro and In Silico Studies of Volatile Compounds from Petroselinum crispum (Mill) Leaves Grown in Saudi Arabia.
Foudah, Ahmed I; Alqarni, Mohammad H; Alam, Aftab; Salkini, Mohammad Ayman; Ross, Samir A; Yusufoglu, Hasan S.
Afiliación
  • Foudah AI; Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 11942, Saudi Arabia.
  • Alqarni MH; Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 11942, Saudi Arabia.
  • Alam A; Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 11942, Saudi Arabia.
  • Salkini MA; Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 11942, Saudi Arabia.
  • Ross SA; National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS 38677, USA.
  • Yusufoglu HS; Department of Biomolecular Sciences, School of Pharmacy, The University of Mississippi, University, MS 38677, USA.
Molecules ; 27(3)2022 Jan 29.
Article en En | MEDLINE | ID: mdl-35164196
ABSTRACT
The herbal plant Petroselinum crispum (P. crispum) (Mill) is commonly available around the world. In this study, the leaves of the herbal plant P. crispum were collected from the central region of Al-Kharj, Saudi Arabia, to explore their in vitro pharmacological activity. Essential oil from the leaves of P. crispum was isolated using the hydrodistillation method. The composition of P. crispum essential oil (PCEO) was determined using Gas chromatography-mass spectrometry (GC-MS). A total of 67 components were identified, representing approximately 96.02% of the total volatile composition. Myristicin was identified as the principal constituent (41.45%). The in vitro biological activity was assessed to evaluate the antioxidant, antimicrobial, and anti-inflammatory potential of PCEO. PCEO showed the highest antimicrobial activity against Candida albicans and Staphylococcus aureus among all the evaluated microbial species. In vitro anti-inflammatory evaluation using albumin and trypsin assays showed the excellent anti-inflammatory potential of PCEO compared to the standard drugs. An in silico study of the primary PCEO compound was conducted using online tools such as PASS, Swiss ADME, and Molecular docking. In silico PASS prediction results supported our in vitro findings. Swiss ADME revealed the drug likeness and safety properties of the major metabolites present in PCEO. Molecular docking results were obtained by studying the interaction of Myristicin with an antifungal (PDB 1IYL and 3LD6), antibacterial (PDB 1AJ6 and 1JIJ), antioxidant (PDB 3NM8 and 1HD2), and anti-inflammatory (3N8Y and 3LN1) receptors supported the in vitro results. Therefore, PCEO or Myristicin might be valuable for developing anti-inflammatory and antimicrobial drugs.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hojas de la Planta / Magnoliopsida Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies País/Región como asunto: Asia Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hojas de la Planta / Magnoliopsida Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies País/Región como asunto: Asia Idioma: En Año: 2022 Tipo del documento: Article