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Patulinervones A and B, two novel α-glucosidase inhibitory spiro-lignans from Melicope patulinervia (Merr. & Chun) C.C. Huang.
Vu, Van-Tuan; Xu, Qi-Qi; Nguyen, Huu Tung; Nguyen, Ngoc-Hieu; Pham, Giang-Nam; Kong, Ling-Yi; Luo, Jian-Guang.
Affiliation
  • Vu VT; Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, PR China.
  • Xu QQ; Faculty of Pharmacy, Phenikaa University, Hanoi, Vietnam.
  • Nguyen HT; Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, PR China.
  • Nguyen NH; Faculty of Pharmacy, Phenikaa University, Hanoi, Vietnam.
  • Pham GN; Faculty of Pharmacy, Phenikaa University, Hanoi, Vietnam.
  • Kong LY; Université Côte d'Azur, Nice Institute of Chemistry UMR 7272, Marine Natural Products Team, Nice, France.
  • Luo JG; Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, PR China.
Nat Prod Res ; 37(21): 3639-3646, 2023.
Article de En | MEDLINE | ID: mdl-35848378
ABSTRACT
(±)-Patulinervones A (1) and B (2), two diastereomers of spiro-lignans sharing an unprecedented dimethyl-spiro[furan-2,2'-furo[2,3-b]furan] 5/5/5 tricyclic moiety were isolated from the leaves of Melicope patulinervia (Merr. & Chun) C.C. Huang. Their structures were established by extensive spectroscopic data and electronic circular dichroism (ECD) analyses. The racemates (±)-1 and 2 and their enantiomers exhibited α-glucosidase inhibitory effect with IC50 values range of 10.08 ± 1.24 - 25.58 ± 1.97 µM.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nat Prod Res Année: 2023 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nat Prod Res Année: 2023 Type de document: Article
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