Bioactive constituents from Clerodendrum trichotomum and their α-glucosidase inhibitory and PPAR-γ agonist activities

Three new neoclerodane diterpenoids (1-3), two new steroids (4-5), one new monoterpene (6), one new derivative of benzaldehyde (7) and one new iridoid glycoside (8), along with 19 known phenolic compounds, were isolated from Clerodendrum trichotomum. Their structures were established by a combination of detailed spectroscopic analyses (1D and 2D NMR) and high resolution electrospray ionization mass spectroscopy (HRESIMS). The isolated compounds were screened on α-glucosidase inhibitory and the peroxisome proliferator-activated receptor gamma (PPAR-γ) agonist activities, and the results showed that three phenylethanoid glycosides, verbascoside (9), leucosceptoside a (10), and isoacteoside (13), and two flavonoids, apigenin (22) and luteolin (26) showed potent inhibitory effects against α-glucosidase, with IC<sub>50</sub> values in the range from 15 to 700 μM. In addition, four flavonoids apigenin 7-O-β-D-glucuronide (19), apigenin (22), luteolin (26), and quercetin (27) exhibited significant PPAR-γ agonistic activities with EC<sub>50</sub> values in the range 2.3-24.9 μM.

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Publication Details

Journal
Fitoterapia
Published
2024-10-20
DOI
https://doi.org/10.1016/j.fitote.2024.106266
Citations
3
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
1.80

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article

Bioactive constituents from Clerodendrum trichotomum and their α-glucosidase inhibitory and PPAR-γ agonist activities

Zhu‐Zhen Han, Yingbo Yang, Meng Wang, Zhengtao Wang et al.
3 citations
Fitoterapia
Phytochemistry and Biological Activities
1.80
article

Bioactive constituents from Clerodendrum trichotomum and their α-glucosidase inhibitory and PPAR-γ agonist activities

Zhu‐Zhen Han, Yingbo Yang, Meng Wang, Zhengtao Wang, Li Yang, Ying Xiao, Hai-Jun Hu, Qian Zhang, Jia Wang
article en
3 citations

Abstract

Three new neoclerodane diterpenoids (1-3), two new steroids (4-5), one new monoterpene (6), one new derivative of benzaldehyde (7) and one new iridoid glycoside (8), along with 19 known phenolic compounds, were isolated from Clerodendrum trichotomum. Their structures were established by a combination of detailed spectroscopic analyses (1D and 2D NMR) and high resolution electrospray ionization mass spectroscopy (HRESIMS). The isolated compounds were screened on α-glucosidase inhibitory and the peroxisome proliferator-activated receptor gamma (PPAR-γ) agonist activities, and the results showed that three phenylethanoid glycosides, verbascoside (9), leucosceptoside a (10), and isoacteoside (13), and two flavonoids, apigenin (22) and luteolin (26) showed potent inhibitory effects against α-glucosidase, with IC<sub>50</sub> values in the range from 15 to 700 μM. In addition, four flavonoids apigenin 7-O-β-D-glucuronide (19), apigenin (22), luteolin (26), and quercetin (27) exhibited significant PPAR-γ agonistic activities with EC<sub>50</sub> values in the range 2.3-24.9 μM.

FitoterapiaVol. 179
Heilongjiang University of Chinese Medicine (CN), Shanghai University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China, Program of Shanghai Academic Research Leader
Zero hunger
Openalex Percentile: Top 13%
Phytochemistry and Biological Activities
1.80
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Bioactive constituents from Clerodendrum trichotomum and their α-glucosidase inhibitory and PPAR-γ agonist activities — Zhu‐Zhen Han, Yingbo Yang, et al. · Fitoterapia (2024) | TGRS Research Map | TGRS