Bioactive pentacyclic triterpenoids from the whole plants of Pterocephalus hookeri. (March 2022)
- Record Type:
- Journal Article
- Title:
- Bioactive pentacyclic triterpenoids from the whole plants of Pterocephalus hookeri. (March 2022)
- Main Title:
- Bioactive pentacyclic triterpenoids from the whole plants of Pterocephalus hookeri
- Authors:
- Zhang, Jun-Sheng
Qian, Yong
Xin, Zhen-Qiang
Cao, Xin-Xin
Yang, Zhou
Zhang, Hua - Abstract:
- Abstract: Eight undescribed triterpenoids (pterohoonoids A−H) including four oleananes, one nor-oleanane and three nor-ursanes, along with seven known analogues, were isolated from the whole plants of Pterocephalus hookeri (Dipsacaceae). The structures with relative stereochemistries of these molecules were elucidated mainly by spectroscopic analyses, and the absolute configurations of the undescribed ones were assigned by a variety of methods, including time-dependent density functional theory (TD-DFT) based electronic circular dichroism (ECD) calculation, Rh2 (OCOCF3 )4 -induced ECD experiment and chemical transformation. The inhibitory effects toward the diabetes target α -glucosidase of all the isolates were assessed, and four of them exhibited pronounced activity with IC50 values ranging from 6.8 to 55.8 μ M. In addition, four compounds also showed inhibition against the nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 macrophage cells (IC50 = 12.4–63.7 μ M). Further assays demonstrated that the most active compound pterohoonoid A inhibited the release of two key pro-inflammatory cytokines TNF- α and IL-6 in a dose-dependent manner. Graphical abstract: Image 1 Highlights: Eight undescribed triterpenoids were isolated from Pterocephalus hookeri. The absolute configurations of the compounds were determined by extensive methods. Four compounds exhibited pronounced inhibitory activity against α-glucosidase. Four compounds exhibited inhibitionAbstract: Eight undescribed triterpenoids (pterohoonoids A−H) including four oleananes, one nor-oleanane and three nor-ursanes, along with seven known analogues, were isolated from the whole plants of Pterocephalus hookeri (Dipsacaceae). The structures with relative stereochemistries of these molecules were elucidated mainly by spectroscopic analyses, and the absolute configurations of the undescribed ones were assigned by a variety of methods, including time-dependent density functional theory (TD-DFT) based electronic circular dichroism (ECD) calculation, Rh2 (OCOCF3 )4 -induced ECD experiment and chemical transformation. The inhibitory effects toward the diabetes target α -glucosidase of all the isolates were assessed, and four of them exhibited pronounced activity with IC50 values ranging from 6.8 to 55.8 μ M. In addition, four compounds also showed inhibition against the nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 macrophage cells (IC50 = 12.4–63.7 μ M). Further assays demonstrated that the most active compound pterohoonoid A inhibited the release of two key pro-inflammatory cytokines TNF- α and IL-6 in a dose-dependent manner. Graphical abstract: Image 1 Highlights: Eight undescribed triterpenoids were isolated from Pterocephalus hookeri. The absolute configurations of the compounds were determined by extensive methods. Four compounds exhibited pronounced inhibitory activity against α-glucosidase. Four compounds exhibited inhibition against the nitric oxide production. The inhibitory effects on pro-inflammatory factors TNF-α and IL-6 were investigated. … (more)
- Is Part Of:
- Phytochemistry. Volume 195(2022)
- Journal:
- Phytochemistry
- Issue:
- Volume 195(2022)
- Issue Display:
- Volume 195, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 195
- Issue:
- 2022
- Issue Sort Value:
- 2022-0195-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-03
- Subjects:
- Pterocephalus hookeri -- Dipsacaceae -- Triterpenoids -- α-glucosidase -- Anti-inflammation
Botanical chemistry -- Periodicals
Biochemistry -- Periodicals
Botany -- Periodicals
Chimie végétale -- Périodiques
572.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00319422 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phytochem.2021.113040 ↗
- Languages:
- English
- ISSNs:
- 0031-9422
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6489.800000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20357.xml