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Alkaloids from Piper longum L and Their Anti-inflammatory Properties.
Tran, Thi Thu Phuong; Dang, Nguyen Hai; Nguyen, Xuan Nhiem; Pham, Hai The; Phan, Uyen Thi Tu; Le, Thanh Huong.
Afiliación
  • Tran TTP; University of Science and Technology of Hanoi, Life Sciences, 18 Hoang Quoc Viet, Hanoi, 10000, Hanoi, VIET NAM.
  • Dang NH; Vietnam Academy of Science and Technology, University of Science and Technology of Hanoi, Hoang Quoc Viet, 18 Hoàng Quoc Viet, Vietnam, 100000, Cau Giay, VIET NAM.
  • Nguyen XN; Vietnamese Academy of Science, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, Hanoi, 10000, Hanoi, VIET NAM.
  • Pham HT; University of Science and Technology of Hanoi, Life Sciences, 18 Hoang Quoc Viet, 10000, Hanoi, VIET NAM.
  • Phan UTT; University of Science and Technology of Hanoi, Life Sciences, 18 Hoang Quoc Viet, 10000, Hanoi, VIET NAM.
  • Le TH; University of Science and Technology of Hanoi, General Education Department, 18 Hoang Quoc Viet, 10000, Hanoi, VIET NAM.
Chem Biodivers ; : e202401224, 2024 Aug 16.
Article en En | MEDLINE | ID: mdl-39149874
ABSTRACT
Piper longum L.(PL)  is considered one of the most important species traditionally used for treating various ailments and has indicated the presence of alkaloids, flavonoids, and steroids. In this study, we isolated the chemical compounds of PLleaves,andmeasuredNO, IL-6, iNOS, as well as COX-2 protein levels. In addition, molecular docking analysis were used to further understand anti-inflammation effect of the compounds. We identified one new alkaloid named piperlongumine A (1) with ten known compounds (2-11). The new compound (1) and two other alkaloids 2E)-3-(4-hydroxy-3-methoxyphenyl)-1-(pyrrol-1-yl)propanone (7) and piperchabamide A (8) significantlyreduced NO production in LPS-stimulated RAW 264.7 cells with the IC50 values of 0.97 ± 0.05 mM, 0.91 ± 0.07mM, 1.63 ± 0.14 mM, respectively. Moreover, at concentration of 2 mM, compound 1 inhibited approximately 98 ± 0.64 % of IL-6 secretion, and decreased  iNOS and COX-2 protein level by about 96 and 19 folds compared to LPS treatment alone, respectively. Furthermore, compounds 1, 7, and 8 were predicted to bind and inhibit IL-6, TNF-a, and iNOS, with compound 1 showing the highest binding energy of -7.09 kcal/mol. This study provides new insights for potential anti-inflammatory drug design and warrants further investigation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Biodivers Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Biodivers Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Suiza