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Chemical constituents from Melicope pteleifolia leaves.
Nguyen, Ngoc Hieu; Ha, Thi Kim Quy; Choi, Sangho; Eum, Sangmi; Lee, Chul Ho; Bach, Tran The; Chinh, Vu Tien; Oh, Won Keun.
Affiliation
  • Nguyen NH; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 151-742, Republic of Korea.
  • Ha TK; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 151-742, Republic of Korea.
  • Choi S; International Biological Material Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 305-806, Republic of Korea.
  • Eum S; International Biological Material Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 305-806, Republic of Korea.
  • Lee CH; International Biological Material Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 305-806, Republic of Korea.
  • Bach TT; Department of Botany, Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, Hanoi, 10307, Viet Nam.
  • Chinh VT; Department of Botany, Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, Hanoi, 10307, Viet Nam.
  • Oh WK; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 151-742, Republic of Korea. Electronic address: wkoh1@snu.ac.kr.
Phytochemistry ; 130: 291-300, 2016 Oct.
Article in En | MEDLINE | ID: mdl-27374481
ABSTRACT
Five acetophenones bearing spiroketal-hexofuranoside rings, one di-C-glycosidic acetophenone and two benzopyrans, along with 16 known compounds were isolated from the leaves of Melicope pteleifolia. Structures of all the isolates were elucidated using extensive spectroscopic methods, including 1D, 2D-NMR and HRESIMS. All the isolates were also evaluated for their neuraminidase inhibitory activities against H1N1, H9N2, wild-type H1N1 and oseltamivir-resistant H1N1 (H274Y mutation) virus strains. Of the isolates, tamarixetin 3-robinobioside was found to exhibit the strongest enzymatic inhibition (IC50 24.93 ± 3.46, 23.19 ± 5.41, 26.67 ± 5.16 and 40.16 ± 4.50 µM, respectively). Selected candidates, kaempferol 3-robinobioside, kaempferol 3-O-ß-d-glucopyranosyl (1 â†’ 2)-α-d-xylopyranoside and tamarixetin 3-robinobioside, also showed moderate reductions in H1N1-induced cytopathic effects on MDCK cells.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Acetophenones / Benzopyrans / Rutaceae Limits: Animals / Humans Language: En Journal: Phytochemistry Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Acetophenones / Benzopyrans / Rutaceae Limits: Animals / Humans Language: En Journal: Phytochemistry Year: 2016 Document type: Article