C17-Labdane diterpenoid alkaloids bearing a rare skeleton with anti-inflammatory and anti-oxidant activities from Forsythia suspensa

Two undescribed C<sub>17</sub>-Labdane diterpenoid alkaloids, named forsylinfenines A and B (1-2), attributable to a rare 4,4,10,13-tetramethyl-1(2),3(4),5(10),6(7)-octahydrobenzo[f]quinolin skeleton, along with three known β-carboline-type alkaloids (3-5), were isolated. The chemical structures including absolute configurations of two undescribed compounds were established by means of integrated spectroscopic techniques and electronic circular dichroism (ECD) calculations. In addition, a plausible biosynthetic pathway for the formation of compounds 1 and 2 was proposed. In vitro, five alkaloids (1-5), especially two undescribed alkaloids with rare skeleton (1-2), exhibited significant anti-inflammatory activities due to inhibiting the release of TNF-α, IL-6, and IL-1β, as well as effective anti-oxidant activities owing to preventing the production of ROS in the LPS-induced RAW264.7 cells.

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Publication Details

Journal
Fitoterapia
Published
2024-12-10
DOI
https://doi.org/10.1016/j.fitote.2024.106345
Citations
3
Primary Topic
Plant Toxicity and Pharmacological Properties
Type
article
Field-Weighted Citation Impact
0.70

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article

C17-Labdane diterpenoid alkaloids bearing a rare skeleton with anti-inflammatory and anti-oxidant activities from Forsythia suspensa

Jia-Huan Liu, Xi‐Dian Yue, Dewu Zhang, Sheng‐Jun Dai et al.
3 citations
Fitoterapia
Plant Toxicity and Pharmacological Properties
0.70
article

C17-Labdane diterpenoid alkaloids bearing a rare skeleton with anti-inflammatory and anti-oxidant activities from Forsythia suspensa

Jia-Huan Liu, Xi‐Dian Yue, Dewu Zhang, Sheng‐Jun Dai, Yue Wang
article en
3 citations

Abstract

Two undescribed C<sub>17</sub>-Labdane diterpenoid alkaloids, named forsylinfenines A and B (1-2), attributable to a rare 4,4,10,13-tetramethyl-1(2),3(4),5(10),6(7)-octahydrobenzo[f]quinolin skeleton, along with three known β-carboline-type alkaloids (3-5), were isolated. The chemical structures including absolute configurations of two undescribed compounds were established by means of integrated spectroscopic techniques and electronic circular dichroism (ECD) calculations. In addition, a plausible biosynthetic pathway for the formation of compounds 1 and 2 was proposed. In vitro, five alkaloids (1-5), especially two undescribed alkaloids with rare skeleton (1-2), exhibited significant anti-inflammatory activities due to inhibiting the release of TNF-α, IL-6, and IL-1β, as well as effective anti-oxidant activities owing to preventing the production of ROS in the LPS-induced RAW264.7 cells.

FitoterapiaVol. 180
Yantai University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
Natural Science Foundation of Shandong Province, Yantai Science and Technology Bureau
Zero hunger
Openalex Percentile: Top 28%
Plant Toxicity and Pharmacological Properties
0.70
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