New Glucosinolates and Alkaloids with Antibacterial Activities from <i>Raphani Semen</i>

Sixteen compounds were isolated from <i>Raphani Semen</i>, including nine new glucosinolate compounds, raseglucosinolate A-I (<b>1</b>-<b>9</b>), four new alkaloids, rasemenine A-D (<b>10</b>-<b>13</b>), two known 4-methylthio-butyl derivatives (<b>14</b>, <b>15</b>), and one known alkaloid (<b>16</b>). Compounds <b>1</b>-<b>13</b> were structurally characterized through a combination of HRESIMS, NMR, UV, IR, and ECD analyses. The potential antibacterial activities of selected compounds were evaluated. Compounds <b>3</b> and <b>10</b> exhibited inhibitory effects against <i>Escherichia coli</i>, with MIC of 32 and 64 μg/mL, respectively. Further mechanistic investigations demonstrated that <b>3</b> exerts its antibacterial activity by compromising the integrity of the cell wall and membrane, resulting in the leakage of intracellular contents and subsequent disruption of cellular metabolism and growth. Molecular docking analysis suggested that DNA gyrase and topoisomerase IV may be potential molecular targets of <b>3</b>. Moreover, the combination of <b>3</b> with ampicillin sodium exhibited an additive antibacterial effect. These studies suggest that <b>3</b> has the potential to become an antibacterial agent and an antibiotic adjuvant.

Authors

Institutions

Publication Details

Journal
Journal of Agricultural and Food Chemistry
Published
2025-09-27
DOI
https://doi.org/10.1021/acs.jafc.5c11051
Primary Topic
Essential Oils and Antimicrobial Activity
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

New Glucosinolates and Alkaloids with Antibacterial Activities from Raphani Semen

Meng‐Qi Yan, Cheng Peng, Zejun Liu, Zhenyue Wang et al.
Journal of Agricultural and Food Chemistry
Essential Oils and Antimicrobial Activity
article

New Glucosinolates and Alkaloids with Antibacterial Activities from Raphani Semen

Meng‐Qi Yan, Cheng Peng, Zejun Liu, Zhenyue Wang, Lihong Wu, Haibo Wu, Sen Li, Kang Yang, Haixue Kuang, De-Qiang Yang, Meng Wang, Ruitong Du
article en

Abstract

Sixteen compounds were isolated from <i>Raphani Semen</i>, including nine new glucosinolate compounds, raseglucosinolate A-I (<b>1</b>-<b>9</b>), four new alkaloids, rasemenine A-D (<b>10</b>-<b>13</b>), two known 4-methylthio-butyl derivatives (<b>14</b>, <b>15</b>), and one known alkaloid (<b>16</b>). Compounds <b>1</b>-<b>13</b> were structurally characterized through a combination of HRESIMS, NMR, UV, IR, and ECD analyses. The potential antibacterial activities of selected compounds were evaluated. Compounds <b>3</b> and <b>10</b> exhibited inhibitory effects against <i>Escherichia coli</i>, with MIC of 32 and 64 μg/mL, respectively. Further mechanistic investigations demonstrated that <b>3</b> exerts its antibacterial activity by compromising the integrity of the cell wall and membrane, resulting in the leakage of intracellular contents and subsequent disruption of cellular metabolism and growth. Molecular docking analysis suggested that DNA gyrase and topoisomerase IV may be potential molecular targets of <b>3</b>. Moreover, the combination of <b>3</b> with ampicillin sodium exhibited an additive antibacterial effect. These studies suggest that <b>3</b> has the potential to become an antibacterial agent and an antibiotic adjuvant.

Journal of Agricultural and Food ChemistryVol. 73(40)
Heilongjiang University of Chinese Medicine (CN), Kementerian Pendidikan Malaysia (MY)
Openalex Percentile: Top 69%
Essential Oils and Antimicrobial Activity
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.