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New lupane-type and ursane-type triterpene saponins from the leaves of Trevesia palmata.
Yen, Pham Hai; Doan, Vu Van; Lien, Giang Thi Kim; Chuong, Nguyen Thi Hong; Thanh, Nguyen Thi Viet; Trang, Do Thi; Dung, Duong Thi; Nhiem, Nguyen Xuan; Tai, Bui Huu; Minh, Chau Van; Kiem, Phan Van.
Afiliação
  • Yen PH; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
  • Doan VV; Graduate University of Science and Technology, VAST, Hanoi, Vietnam.
  • Lien GTK; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
  • Chuong NTH; The University of Danang, Danang, Vietnam.
  • Thanh NTV; University of Education, The University of Danang, Danang, Vietnam.
  • Trang DT; School of Chemical Engineering, Hanoi University of Science and Technology, Hanoi, Vietnam.
  • Dung DT; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
  • Nhiem NX; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
  • Tai BH; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
  • Minh CV; Graduate University of Science and Technology, VAST, Hanoi, Vietnam.
  • Kiem PV; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi Vietnam.
Nat Prod Res ; 35(19): 3285-3292, 2021 Oct.
Article em En | MEDLINE | ID: mdl-31790291
ABSTRACT
Three new triterpene saponins including two lupane-types and an ursane-type were isolated from the leaves of Trevesia palmata. Their structures were determined as 2α,3ß,23-trihydroxylup-20(29)-en-28-oic acid 3-O-α-L-arabinopyranoside (1), 2α,3ß,23-trihydroxylup-20(29)-en-28-oic acid 3-O-[α-L-arabinopyranoside]-28-O-[ß-D-glucopyranosyl] ester (2), and 2α,3ß,23-trihydroxyurs-12-en-28-oic acid 3-O-[α-L-arabinopyranoside]-28-O-[ß-D-glucopyranosyl(1→2)-ß-D-glucopyranosyl] ester (3) by analysis of their HR-ESI-MS, 1D and 2D NMR spectra. The 2α,3ß,23-trioxygenated pentacyclic triterpenes were uncommonly found in the nature. At concentration of 100 µM, compounds 1-3 inhibited NO production in LPS activated BV2 cells with inhibitory rates of 17.4 ± 1.8%, 33.1 ± 1.2%, and 11.7 ± 2.2%, respectively. But, they did not significantly inhibit yeast α-glucosidase activity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saponinas / Triterpenos / Araliaceae / Triterpenos Pentacíclicos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saponinas / Triterpenos / Araliaceae / Triterpenos Pentacíclicos Idioma: En Ano de publicação: 2021 Tipo de documento: Article