Flavonoids from Pistacia chinensis subsp. integerrima with leishmanicidal activity: computational and experimental evidence.

Autor: Rauf A; Department of Chemistry, University of Swabi, Swabi, Khyber Pakhtunkhwa, Pakistan., Rashid U; Department of Chemistry, COMSATS University Islamabad, Abbottabad Campus, Abbottabad, Pakistan., Shbeer AM; Department of Surgery, Faculty of Medicine, Jazan University, Jazan, Saudi Arabia., Al-Ghorbani M; Department of Chemistry, Faculty of Science and Arts, Ulla, Taibah University, Medina, Saudi Arabia., Muhammad N; Department of Pharmacy, Abdul Wali Khan University, Mardan, Khyber Pakhtunkhwa, Pakistan., Khalil AA; University Institute of Diet and Nutritional Sciences, Faculty of Allied Health Sciences, The University of Lahore, Lahore, Pakistan., Naz H; Department of Biotechnology, Shaheed Benazir Bhutto Women University Peshawar, Peshawar, Khyber Pakhtunkhwa, Pakistan., Sharma R; Department of Rasa Shastra and Bhaishajya Kalpana, Faculty of Ayurveda, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India., Ribaudo G; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Jazyk: angličtina
Zdroj: Natural product research [Nat Prod Res] 2024 Sep; Vol. 38 (18), pp. 3282-3287. Date of Electronic Publication: 2023 Jun 26.
DOI: 10.1080/14786419.2023.2228459
Abstrakt: Pistacia chinensis subsp. integerrima is a valuable medicinal plant as its parts and extracts found application for treating diarrhea, fever, liver disorders, asthma, and inflammation. In this study, we report the leishmanicidal activity of sakuranetin, spinacetin, and patuletin extracted from P. chinensis . The tested compounds revealed a strong anti-leishmanial activity in vitro against Leishmania major showing IC 50 values of 7.98 ± 0.16 µM, 9.23 ± 0.23 µM 11.09 ± 0.87 µM for sakuranetin, spinacetin, and patuletin, respectively. Moreover, to explore the potential mechanism(s) by which the compounds may act, computational docking studies were performed against dihydrofolate reductase and pteridine reductase, showing that the flavonoids could target these two key enzymes to exploit their leishmanicidal activity. In accordance with in vitro results, patuletin was highlighted as the most promising compound of the set, and binding energy values of -6.72 and -6.74 kcal/mol were computed for the two proteins, respectively.
Databáze: MEDLINE