Xuelin Chen , Hanlei Wang , Kun Zhang , Jing Lu , Yumei Zhang
{"title":"Chemical constituents from the fruits of Kochia scoparia and their chemotaxonomic significance","authors":"Xuelin Chen , Hanlei Wang , Kun Zhang , Jing Lu , Yumei Zhang","doi":"10.1016/j.bse.2025.105141","DOIUrl":"10.1016/j.bse.2025.105141","url":null,"abstract":"<div><div>For the phytochemical studies of the fruits of <em>Kochia scoparia</em> (L.) Schrad. (Kochiae Fructus, KF), we isolated chemical components from KF. Twenty compounds, including six alkaloids (<strong>1</strong>–<strong>6</strong>), nine polyphenols (<strong>7</strong>–<strong>15</strong>), three flavonoids (<strong>16</strong>–<strong>18</strong>), and two sterols (<strong>19</strong>–<strong>20</strong>) were isolated and identified from the ethanol extract of KF by chromatographic and spectroscopic techniques. Compounds <strong>2</strong>, <strong>3</strong>, and <strong>5</strong>–<strong>16</strong> were isolated from KF and <em>Kochia</em> genus for the first time. Furthermore, by discussing the taxonomic significance of these secondary metabolites, we found that Araliaceae, Compositae, Ranunculaceae, and Leguminosae might have a close evolutionary relationship. In conclusion, these results provide new insights into the chemical diversity and chemotaxonomic significance of <em>K. scoparia</em> in the <em>Kochia</em> genus and the Chenopodiaceae family.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105141"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145106553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Phytochemical and chemotaxonomic study on Saussurea medusa Maxim. (Compositae) Ⅱ","authors":"Nan Wu , Ruitao Yu","doi":"10.1016/j.bse.2025.105174","DOIUrl":"10.1016/j.bse.2025.105174","url":null,"abstract":"<div><div>A phytochemical investigation of <em>Saussurea medusa</em> Maxim. led to the isolation of ten compounds, including salicifoliol (<strong>1</strong>), 1-hydroxy-6-epipinoresinol (<strong>2</strong>), (7<em>R</em>,7′<em>R</em>,7″<em>R</em>,8<em>S</em>,8′<em>S</em>,8″<em>S</em>)-4′,4″-dihydroxy-3,3′,3″,5-tetramethoxy-7,9':7′,9-diepoxy-4,8″-oxy-8,8′-sesquineolignan-7″,9″-diol (<strong>3</strong>), diarctigenin (<strong>4</strong>), quercetin 3-rutinoside-7-glucoside (<strong>5</strong>), isololiolide (<strong>6</strong>), (<em>E</em>)-3-(3′-hydroxybut-1′-enyl)-2,4,4-trimethylcyclohexa-2,5-dien-1-one (<strong>7</strong>), (3<em>S</em>,5<em>R</em>,8<em>R</em>)-3,5-dihydroxymegastigma-6,7-dien-9-one (<strong>8</strong>), crotonine (<strong>9</strong>), and nudifloric acid (<strong>10</strong>). The structures of these compounds were elucidated based on spectroscopic analysis and comparison with previously reported data. All isolated compounds (<strong>1</strong>–<strong>10</strong>) are reported from <em>S. medusa</em> for the first time, with compounds <strong>1</strong>, <strong>5</strong>, 6<strong>, 8</strong>, and <strong>9</strong> being new to the genus <em>Saussurea</em>, and compounds <strong>2</strong>, <strong>3</strong>, <strong>7</strong>, and <strong>10</strong> being new to the Compositae family. The chemotaxonomic significance of these isolated compounds was discussed.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105174"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145525878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chemical constituents from Helvella leucopus and their chemotaxonomic significance","authors":"Zhao-Zhao Zhang , Yi-Yang Xie , Li-Ping Teng , Zhong-Bo Zhou","doi":"10.1016/j.bse.2025.105159","DOIUrl":"10.1016/j.bse.2025.105159","url":null,"abstract":"<div><div>Phytochemical investigation of <em>Helvella</em> <em>l</em><em>eucopus</em> led to the isolation of thirteen compounds, comprising six nucleosides <strong>(1</strong>–<strong>6</strong>), one pyrimidine (<strong>7</strong>), one fatty acid (<strong>8</strong>), one sterol (<strong>9</strong>), one indole derivative (<strong>10</strong>), one pyridine derivative (<strong>11</strong>), one heterocyclic compound (<strong>12</strong>) and one amino acid (<strong>13</strong>). Significantly, with the exception of compounds <strong>7</strong> and <strong>9</strong>, all other compounds were isolated from <em>H</em>. <em>l</em><em>eucopus</em> for the first time. Additionally, compounds <strong>8</strong> and <strong>10</strong>–<strong>12</strong> represent the first reports of their presence in the Helvellaceae family. The chemotaxonomic implications of these findings were also discussed in this study.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105159"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145424692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hao Fan , Pingping Wu , Xin Wang , Yuze Li , Chong Deng , Wei Wang , Xiaomei Song , Xin Zhang , Dongdong Zhang
{"title":"OSMAC-activated and GNPS-guided investigation of alkaloids from an endophytic fungus Aspergillus sp. FH-1 of Valeriana officinalis L.","authors":"Hao Fan , Pingping Wu , Xin Wang , Yuze Li , Chong Deng , Wei Wang , Xiaomei Song , Xin Zhang , Dongdong Zhang","doi":"10.1016/j.bse.2025.105151","DOIUrl":"10.1016/j.bse.2025.105151","url":null,"abstract":"<div><div>Guided by an integrated OSMAC and GNPS molecular networking strategy, a chemical investigation of the endophytic fungus <em>Aspergillus</em> sp. FH-1, isolated from <em>Valeriana officinalis</em> L., yielded sixteen alkaloids (<strong>1</strong>–<strong>16</strong>), including one new compound (<strong>1</strong>) and 15 known ones (<strong>2</strong>–<strong>16</strong>). The structures of all compounds were unambiguously elucidated by comprehensive spectroscopic analyses (including HRESIMS, 1D and 2D NMR) and by comparison with literature data. Notably, compounds <strong>13</strong> and <strong>14</strong> were discovered from a microbial source for the first time. Compounds <strong>2</strong> and <strong>3</strong> were isolated from the genus <em>Aspergillus</em> for the first time, while compounds <strong>4</strong>–<strong>7</strong>, <strong>11</strong>, <strong>12</strong>, and <strong>15</strong> were reported from this specific fungus for the first time. In bioactivity assays, compounds <strong>1</strong>–<strong>4</strong>, <strong>7</strong>, <strong>12</strong>, and <strong>14</strong> exhibited significant antifungal activity against the phytopathogen <em>Colletotrichum gloeosporioides</em>, with EC<sub>50</sub> values ranging from 28.54 ± 1.34 to 83.74 ± 1.12 μg/mL. Furthermore, the chemotaxonomic significance of these alkaloids within the genus <em>Aspergillus</em> is also discussed.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105151"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145333158","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jin-Xin Zhu , Ze-Yu Zhao , Chi Song , Juan Xiong , Jin-Feng Hu
{"title":"Chemical constituents from the endangered tertiary relict conifer Pseudotaxus chienii (W. C. Cheng) W. C. Cheng and their chemotaxonomic significance","authors":"Jin-Xin Zhu , Ze-Yu Zhao , Chi Song , Juan Xiong , Jin-Feng Hu","doi":"10.1016/j.bse.2025.105136","DOIUrl":"10.1016/j.bse.2025.105136","url":null,"abstract":"<div><div>The white-berry yew [<em>Pseudotaxus chienii</em> (W. C. Cheng) W. C. Cheng], a monotypic species of the genus within the family Taxaceae, is an endangered Chinese endemic relict conifer. A preliminary phytochemical investigation on the ethyl acetate soluble fraction of the 90 % methanol extract from the renewable twigs and needles of <em>P. chienii</em> resulted in the isolation and characterization of 14 compounds, including one <em>δ-</em>tocopherol derivative (<strong>1</strong>), one <em>nor</em>-labdane (<strong>2</strong>) with a rare C14-skeleton, two taxoids (<strong>3</strong>, <strong>4</strong>), one abietane-type diterpenoid (<strong>5</strong>), five <em>ent</em>-kaurane-type diterpenoids (<strong>6</strong>–<strong>10</strong>), one isopimarane-type diterpenoid (<strong>11</strong>), and three pentacyclic triterpenoids (<strong>12</strong>–<strong>14</strong>). Among them, compound <strong>1</strong> is previously undescribed. Compound <strong>2</strong> is reported herein as a new natural product. This study also briefly discussed the chemotaxonomic significance of the isolated taxane-type compounds (<strong>3</strong>, <strong>4</strong>), which were obtained from the genus <em>Pseudotaxus</em> for the first time.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105136"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145046802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Khadijeh Rihai Rad , Alireza Babaei , Mahmoud Kiani , Daniel Potter , Hamidreza Ardalani
{"title":"Metabolome fingerprinting elucidates chemodiversity in Ornithogalum, Loncomelos, and Melomphis (Asparagaceae)","authors":"Khadijeh Rihai Rad , Alireza Babaei , Mahmoud Kiani , Daniel Potter , Hamidreza Ardalani","doi":"10.1016/j.bse.2025.105121","DOIUrl":"10.1016/j.bse.2025.105121","url":null,"abstract":"<div><div>This research employed GC-MS metabolomics profiling on bulbs of three genera i.e., <em>Ornithogalum</em>, <em>Loncomelos</em>, and <em>Melomphis</em> (Asparagaceae), to elucidate their taxonomic relationships. The analysis of 30 specimens across 8 species (<em>Ornithogalum</em> comprising 3 species: <em>O. cuspidatum</em>, <em>O. neurostegium</em>, <em>O. orthophyllum</em>; <em>Loncomelos</em> including 4 species: <em>L. arcuatum</em>, <em>L. brachystachys</em>, <em>L. bungei</em>, <em>L. kurdicum</em>; and <em>Melomphis persica</em>) from Iran revealed 147 detected metabolites, classified in several main superclasses e.g., organic oxygen compounds (40 %), organic acids (23 %), and lipids (18 %). Additionally, the metabolites were grouped into classes, with carbohydrates comprising the majority (42 %), followed by carboxylic acids (17 %) and fatty acids (14 %). Multivariate statistics including the variable importance in projection, and hierarchical clustering heat map discerned metabolites differentiating the genera. Projections to latent structures discriminant analysis revealed that <em>Ornithogalum</em> exhibited significant metabolic divergence from the closely related taxa <em>Loncomelos</em> and <em>Melomphis</em>, aligning with their established phylogenetic divisions. Overall, this work significantly expands knowledge of the chemodiversity of these taxa. The findings provide a phylogenetic framework to guide further ethno-pharmacological, phytochemical, and evolutionary research on these geophyte taxa.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105121"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145046803","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yan Piao , Ze Wu , Yue Zhang, Qiong Wu, Jinglin Piao, Mengwei Gao, Fang Ye, Changhao Zhang, Lili Jin
{"title":"Chemical constituents of Parasenecio auriculatus (DC.) H. koyama and their chemotaxonomic significance","authors":"Yan Piao , Ze Wu , Yue Zhang, Qiong Wu, Jinglin Piao, Mengwei Gao, Fang Ye, Changhao Zhang, Lili Jin","doi":"10.1016/j.bse.2025.105143","DOIUrl":"10.1016/j.bse.2025.105143","url":null,"abstract":"<div><div>A total of 18 compounds were isolated from whole <em>Parasenecio auriculatus</em> (DC.) H. Koyama plants, including eleven flavonoids (<strong>1</strong>–<strong>11</strong>), four mono-phenols (<strong>12</strong>–<strong>15</strong>), one triterpenoid (<strong>16</strong>), one coumarin (<strong>17</strong>), and one sterol (<strong>18</strong>). The chemical structures of these compounds were determined via nuclear magnetic resonance spectroscopy and mass spectrometry, then compared with published chemical structural data. All compounds were isolated from <em>P</em>. <em>auriculatus</em> for the first time, while compounds <strong>4</strong>, <strong>5</strong>, <strong>7</strong> and <strong>10</strong> were isolated from a species in the genus <em>Parasenecio</em> for the first time. The chemotaxonomic significance of these compounds is discussed.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105143"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145109782","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sesquiterpenoids from the aerial parts of Hypericum lancasteri (Hypericaceae) and their chemotaxonomic significance","authors":"Qi Zhou , Jiang Wan , Chun-Xiao Jiang , Shou-Yuan Wu , Peng-Jun Zhou , Ying-Peng Tong","doi":"10.1016/j.bse.2025.105145","DOIUrl":"10.1016/j.bse.2025.105145","url":null,"abstract":"<div><div>The phytochemical investigation on the aerial parts of <em>Hypericum lancasteri</em> led to the isolation and characterization of eight sesquiterpenoids, including an undescribed one belonging to guaiane-type (<strong>1</strong>) and seven known sesquiterpenoids (<strong>2</strong>–<strong>7</strong>). The structure of the new compound was elucidated by spectroscopic techniques, including 1D-/2D-NMR spectroscopy and HR-ESI-MS analysis. The known compounds were identified by comparison of their observed physicochemical properties and spectroscopic data with those reported in the literature. Notably, all isolated sesquiterpenoids were obtained from <em>H. lancasteri</em> for the first time, and compounds <strong>1</strong>–<strong>6</strong> and <strong>8</strong> are reported here for the first time in the family Hypericaceae. The taxonomic significance of these isolated sesquiterpenoids was discussed, contributing to a broader understanding of the chemotaxonomic classification within the family Hypericaceae.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105145"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145227419","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zhen-Xiang Liu , Lin-Fen Ding , Ye-Ting Shi , Zhou Liu , Shi-Huan Yin , Qiu-Ye Zhao , Liu-Dong Song , Xing-De Wu
{"title":"Chemical constituents from the fruits of Illicium henryi Diels and their chemotaxonomic significance","authors":"Zhen-Xiang Liu , Lin-Fen Ding , Ye-Ting Shi , Zhou Liu , Shi-Huan Yin , Qiu-Ye Zhao , Liu-Dong Song , Xing-De Wu","doi":"10.1016/j.bse.2025.105144","DOIUrl":"10.1016/j.bse.2025.105144","url":null,"abstract":"<div><div>A phytochemical investigation of <em>Illicium henryi</em> fruits resulted in the identification of 31 compounds, including fourteen sesquiterpenoids (<strong>1</strong>–<strong>14</strong>), two flavonoids (<strong>15</strong>–<strong>16</strong>), seven lignans (<strong>17</strong>–<strong>23</strong>), one shikimic acid derivative (<strong>24</strong>), one phenylpropanoid derivative (<strong>25</strong>), two phenolic compounds (<strong>26</strong> and <strong>27</strong>), three monoterpenoids (<strong>28</strong>–<strong>30</strong>), and one C13 norsesquiterpenoid (<strong>31</strong>). The structures of these compounds were elucidated through <sup>1</sup>H and <sup>13</sup>C NMR spectroscopic analyses and comparison with previously documented data. Twenty compounds (<strong>2</strong>–<strong>4</strong>, <strong>8</strong>, <strong>9</strong>, <strong>14</strong>, <strong>15</strong>, <strong>17</strong>–<strong>19</strong>, <strong>21</strong>, and <strong>23</strong>–<strong>31</strong>) were isolated from <em>I. henryi</em> for the first time, and among them, eleven compounds (<strong>15</strong>, <strong>17</strong>–<strong>19</strong>, <strong>23</strong>, <strong>25</strong>–<strong>28</strong>, <strong>30</strong>, and <strong>31</strong>) had never been previously isolated from any <em>Illicium</em> species. Additionally, this article discusses the chemotaxonomic significance of these compounds.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105144"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145109781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Guy Paulin M. Kemayou , Ya-shi Wang , Wen-Chao Zhou , Gervais M. Happi , Shi-qi Liu , Wei Su , Bin Li , Simeon F. Kouam , Wei Wang , Yu-pei Yang
{"title":"Hepatoprotective compounds from fruits of Kadsura coccinea (Lem.) A. C. Smith (Schisandraceae) and their chemotaxonomic significance","authors":"Guy Paulin M. Kemayou , Ya-shi Wang , Wen-Chao Zhou , Gervais M. Happi , Shi-qi Liu , Wei Su , Bin Li , Simeon F. Kouam , Wei Wang , Yu-pei Yang","doi":"10.1016/j.bse.2025.105147","DOIUrl":"10.1016/j.bse.2025.105147","url":null,"abstract":"<div><div>A phytochemical investigation of <em>Kadsura coccinea</em> fruits resulted in the isolation of twenty-eight secondary metabolites, including twenty-four lignans (<strong>1−24</strong>), a triterpenoid (<strong>25</strong>), a steroid (<strong>26</strong>), a shikimic acid (<strong>27</strong>), and a furan derivative (<strong>28</strong>). The structures of these compounds were identified using extensive spectroscopic methods, as well as comparison with literature data. To the best of our knowledge, compounds <strong>9</strong>, <strong>13−15</strong>, <strong>21</strong>, and <strong>25−28</strong> were newly isolated from <em>Kadsura coccinea</em>, and compounds <strong>14</strong>, <strong>27,</strong> and <strong>28</strong> were isolated from the genus <em>Kadsura</em> for the first time. All the isolated compounds were evaluated for their hepatoprotective activity against APAP-induced toxicity in HepG-2 cells. Kadsuphilol A (<strong>1</strong>) showed significant hepatoprotective activity, with a cell survival rate of 60.7 ± 1.5 % at 20 μM (positive control, bicyclol, 60.4 ± 1.6 %). The lignans (<strong>2−17</strong>) exhibited moderate activity, with cell survival rates ranging from 49.3 ± 1.0 % to 56.5 ± 0.9 %. The structure-activity relationship of the tested compounds was investigated, and their chemotaxonomic significance was also discussed.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"124 ","pages":"Article 105147"},"PeriodicalIF":2.0,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145262930","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}