Chemical constituents of the seeds of <i>Citrus reticulata</i> and their bioactivity

Four new limonoids (<b>1-4</b>), reticulactone A <b>(1)</b>, 21,23-dihydro-23-ethoxy-21-oxolimonin <b>(2)</b>, tetrahydro-20,22-dihydroxy-21,23-diethoxy-nomilin <b>(3)</b>, and dasycarinone B <b>(4)</b>, as well as 11 known limonoids and one known carbolic acid, were isolated from the EtOH extract of the seeds of <i>Citrus reticulata</i> Blanco. The inhibitory effects of 15 limonoids (<b>1</b>-<b>15</b>) on the proliferation of HepG2 liver cancer cells were evaluated using the CCK-8 assay. Based on their structural characteristics, the results revealed that the typical limonoid compounds <b>2</b>, <b>5</b>, <b>10</b>, and <b>12</b> exhibited stronger cytotoxicity compared to other limonoid compounds. Notably, the novel compound <b>2</b> demonstrated the strongest cytotoxic activity (IC<sub>50</sub> = 18.24 ± 2.78 μM).

Authors

Institutions

Publication Details

Journal
Journal of Asian Natural Products Research
Published
2026-02-09
DOI
https://doi.org/10.1080/10286020.2026.2625940
Primary Topic
Phytochemical compounds biological activities
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Chemical constituents of the seeds of Citrus reticulata and their bioactivity

Gui‐Xin Chou, Hong-Tao Xu, Jun-Jie Yang, Meng-Jue Rui
Journal of Asian Natural Products Research
Phytochemical compounds biological activities
article

Chemical constituents of the seeds of Citrus reticulata and their bioactivity

Gui‐Xin Chou, Hong-Tao Xu, Jun-Jie Yang, Meng-Jue Rui
article en

Abstract

Four new limonoids (<b>1-4</b>), reticulactone A <b>(1)</b>, 21,23-dihydro-23-ethoxy-21-oxolimonin <b>(2)</b>, tetrahydro-20,22-dihydroxy-21,23-diethoxy-nomilin <b>(3)</b>, and dasycarinone B <b>(4)</b>, as well as 11 known limonoids and one known carbolic acid, were isolated from the EtOH extract of the seeds of <i>Citrus reticulata</i> Blanco. The inhibitory effects of 15 limonoids (<b>1</b>-<b>15</b>) on the proliferation of HepG2 liver cancer cells were evaluated using the CCK-8 assay. Based on their structural characteristics, the results revealed that the typical limonoid compounds <b>2</b>, <b>5</b>, <b>10</b>, and <b>12</b> exhibited stronger cytotoxicity compared to other limonoid compounds. Notably, the novel compound <b>2</b> demonstrated the strongest cytotoxic activity (IC<sub>50</sub> = 18.24 ± 2.78 μM).

Journal of Asian Natural Products Research
Shanghai University of Traditional Chinese Medicine (CN), Jilin Academy of Traditional Chinese Medicine (CN)
Openalex Percentile: Top 63%
Phytochemical compounds biological activities
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Chemical constituents of the seeds of <i>Citrus reticulata</i> and their bioactivity — Gui‐Xin Chou, Hong-Tao Xu, et al. · Journal of Asian Natural Products Research (2026) | TGRS Research Map | TGRS