Wei Wei , Jing-Hui Yin , Bang-Yong Wang , Lin-Lin Luo , Xiao-Xiao Mo , Qin-Gang Tan
{"title":"花椒中具有细胞毒活性的生物碱。","authors":"Wei Wei , Jing-Hui Yin , Bang-Yong Wang , Lin-Lin Luo , Xiao-Xiao Mo , Qin-Gang Tan","doi":"10.1016/j.fitote.2025.106913","DOIUrl":null,"url":null,"abstract":"<div><div>Two previously undescribed alkaloids, 8-<em>O</em>-demethylmaclekarpine D (<strong>1</strong>) and zanthonitine (<strong>2</strong>), along with a pair of inseparable rotamers, 4-hydroxyl-beecheyamide (<strong>3a</strong>) and (<em>E</em>)-3-(4-hydroxy-3-methoxyphenyl)-<em>N</em>-(4-methoxyphenethyl)-<em>N-</em>methylacrylamide (<strong>3b</strong>), were isolated from <em>Zanthoxylum nitidum</em>. These compounds were accompanied by 35 known alkaloids, including benzophenanthridines (<strong>4–21</strong>), quinolines (<strong>22</strong>−<strong>31</strong>), aporphines (<strong>32</strong>–<strong>35</strong>) and other structural types (<strong>36–38</strong>). Structural elucidation was achieved through comprehensive spectroscopic analyses, including NMR, HRESIMS, X-ray crystallography, ECD and calculated <sup>13</sup>C NMR DP4+ analysis. Cytotoxicity evaluation revealed compounds <strong>6</strong>, <strong>7</strong>, <strong>18</strong> and <strong>33</strong> (IC<sub>50</sub> = 7.29–22.90 μM) exhibited potent inhibitory effects on the proliferation of HepG2 cells, outperforming the efficacy of doxorubicin (IC<sub>50</sub> = 28.92 ± 0.48 μM). Similarly, compounds <strong>9</strong>, <strong>16</strong> and <strong>21</strong> (IC<sub>50</sub> = 21.77–25.13 μM) suppressed SW480 cells, superior to doxorubicin (IC<sub>50</sub> = 31.15 ± 0.24 μM).</div></div>","PeriodicalId":12147,"journal":{"name":"Fitoterapia","volume":"187 ","pages":"Article 106913"},"PeriodicalIF":2.6000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Alkaloids with cytotoxic activities from Zanthoxylum nitidum\",\"authors\":\"Wei Wei , Jing-Hui Yin , Bang-Yong Wang , Lin-Lin Luo , Xiao-Xiao Mo , Qin-Gang Tan\",\"doi\":\"10.1016/j.fitote.2025.106913\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Two previously undescribed alkaloids, 8-<em>O</em>-demethylmaclekarpine D (<strong>1</strong>) and zanthonitine (<strong>2</strong>), along with a pair of inseparable rotamers, 4-hydroxyl-beecheyamide (<strong>3a</strong>) and (<em>E</em>)-3-(4-hydroxy-3-methoxyphenyl)-<em>N</em>-(4-methoxyphenethyl)-<em>N-</em>methylacrylamide (<strong>3b</strong>), were isolated from <em>Zanthoxylum nitidum</em>. These compounds were accompanied by 35 known alkaloids, including benzophenanthridines (<strong>4–21</strong>), quinolines (<strong>22</strong>−<strong>31</strong>), aporphines (<strong>32</strong>–<strong>35</strong>) and other structural types (<strong>36–38</strong>). Structural elucidation was achieved through comprehensive spectroscopic analyses, including NMR, HRESIMS, X-ray crystallography, ECD and calculated <sup>13</sup>C NMR DP4+ analysis. Cytotoxicity evaluation revealed compounds <strong>6</strong>, <strong>7</strong>, <strong>18</strong> and <strong>33</strong> (IC<sub>50</sub> = 7.29–22.90 μM) exhibited potent inhibitory effects on the proliferation of HepG2 cells, outperforming the efficacy of doxorubicin (IC<sub>50</sub> = 28.92 ± 0.48 μM). Similarly, compounds <strong>9</strong>, <strong>16</strong> and <strong>21</strong> (IC<sub>50</sub> = 21.77–25.13 μM) suppressed SW480 cells, superior to doxorubicin (IC<sub>50</sub> = 31.15 ± 0.24 μM).</div></div>\",\"PeriodicalId\":12147,\"journal\":{\"name\":\"Fitoterapia\",\"volume\":\"187 \",\"pages\":\"Article 106913\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fitoterapia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0367326X25005398\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fitoterapia","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0367326X25005398","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Alkaloids with cytotoxic activities from Zanthoxylum nitidum
Two previously undescribed alkaloids, 8-O-demethylmaclekarpine D (1) and zanthonitine (2), along with a pair of inseparable rotamers, 4-hydroxyl-beecheyamide (3a) and (E)-3-(4-hydroxy-3-methoxyphenyl)-N-(4-methoxyphenethyl)-N-methylacrylamide (3b), were isolated from Zanthoxylum nitidum. These compounds were accompanied by 35 known alkaloids, including benzophenanthridines (4–21), quinolines (22−31), aporphines (32–35) and other structural types (36–38). Structural elucidation was achieved through comprehensive spectroscopic analyses, including NMR, HRESIMS, X-ray crystallography, ECD and calculated 13C NMR DP4+ analysis. Cytotoxicity evaluation revealed compounds 6, 7, 18 and 33 (IC50 = 7.29–22.90 μM) exhibited potent inhibitory effects on the proliferation of HepG2 cells, outperforming the efficacy of doxorubicin (IC50 = 28.92 ± 0.48 μM). Similarly, compounds 9, 16 and 21 (IC50 = 21.77–25.13 μM) suppressed SW480 cells, superior to doxorubicin (IC50 = 31.15 ± 0.24 μM).
期刊介绍:
Fitoterapia is a Journal dedicated to medicinal plants and to bioactive natural products of plant origin. It publishes original contributions in seven major areas:
1. Characterization of active ingredients of medicinal plants
2. Development of standardization method for bioactive plant extracts and natural products
3. Identification of bioactivity in plant extracts
4. Identification of targets and mechanism of activity of plant extracts
5. Production and genomic characterization of medicinal plants biomass
6. Chemistry and biochemistry of bioactive natural products of plant origin
7. Critical reviews of the historical, clinical and legal status of medicinal plants, and accounts on topical issues.