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Terpenoids from the Stems of Fissistigma polyanthoides and Their Anti-Inflammatory Activity.
Nguyen Ngoc, Hieu; Alilou, Mostafa; Stonig, Marlies; Nghiem, Duc Trong; Kim, Le Thien; Gostner, Johanna M; Stuppner, Hermann; Ganzera, Markus.
Afiliação
  • Nguyen Ngoc H; Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI) , University of Innsbruck , 6020 Innsbruck , Austria.
  • Alilou M; Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI) , University of Innsbruck , 6020 Innsbruck , Austria.
  • Stonig M; Division of Medical Biochemistry, Biocenter , Medical University of Innsbruck , 6020 Innsbruck , Austria.
  • Nghiem DT; Department of Botany , Hanoi University of Pharmacy , Hoan Kiem , Hanoi 100000 , Vietnam.
  • Kim LT; Department of Botany , Hanoi University of Pharmacy , Hoan Kiem , Hanoi 100000 , Vietnam.
  • Gostner JM; Division of Medical Biochemistry, Biocenter , Medical University of Innsbruck , 6020 Innsbruck , Austria.
  • Stuppner H; Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI) , University of Innsbruck , 6020 Innsbruck , Austria.
  • Ganzera M; Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI) , University of Innsbruck , 6020 Innsbruck , Austria.
J Nat Prod ; 82(11): 2941-2952, 2019 11 22.
Article em En | MEDLINE | ID: mdl-31626544
Twelve new terpenoids (1-12) were isolated from the stems of Fissistigma polyanthoides, an anti-inflammatory medicinal plant traditionally used in Vietnam. Most of them (1-9) possess a sesquiterpenoid backbone (e.g., guaiane, germacrane, and cadinane) connected to a 2'-O-trans-cinnamoyl)-ß-d-glucopyranose moiety, which is rare in Nature. Among them, compounds 4 (5/8-fused ring) and 6 (spiran [4,5] ring) represent uncommonly rearranged sesquiterpenoids. Compounds 10-12 are a novel monoterpene and two megastigmane derivatives, respectively. The individual structures were elucidated by combining NMR and MS data, and their configuration was established in NOESY and ECD experiments. Compounds 1-9 were also examined for their potential to interact with nuclear factor-kappa B activator protein 1 (NF-κB/AP-1) signaling by using the myelomonocytic reporter cell line THP-1Blue-CD14. Compounds 1-5 showed dose-dependent inhibitory effects [IC50 13.7 µM (1) to 49.0 µM (5)] on lipopolysaccharide-stimulated cells. However, compounds 1 to 4 also negatively affected cell viability in the same concentration range, while compound 5 was less potently cytotoxic.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terpenos / Anti-Inflamatórios não Esteroides / Caules de Planta / Annonaceae Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Nat Prod Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Áustria País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terpenos / Anti-Inflamatórios não Esteroides / Caules de Planta / Annonaceae Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Nat Prod Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Áustria País de publicação: Estados Unidos