Lian Yang, Dong-Mei Lin, Xiu-Ming Cui, Xiao-Yan Yang
{"title":"Four Alkaloids from the Rice Fermentation of Fungus Penicillium expansum","authors":"Lian Yang, Dong-Mei Lin, Xiu-Ming Cui, Xiao-Yan Yang","doi":"10.1007/s10600-025-04744-w","DOIUrl":"10.1007/s10600-025-04744-w","url":null,"abstract":"<p>One pyrrolizidine alkaloid, (3<i>S</i>,4<i>S</i>,5<i>R</i>,6<i>R</i>)-penexpandine (<b>1</b>), and three indole alkaloids, 11<i>S</i>-(–)-penilloid A (<b>2</b>), roquefortine C (<b>3</b>), and roquefortine D (<b>4</b>), were isolated from the rice fermentation of the fungus <i>Penicillium expansum</i>. Their structures were established through NMR spectroscopic data analysis and comparison with reported data. The structure and absolute configuration of compound <b>1</b> were elucidated based on comprehensive spectroscopic analysis and electronic circular dichroism (ECD) calculations. Ultimately, the absolute configuration of compound <b>1</b> was determined for the first time as (3<i>S</i>,4<i>S</i>,5<i>R</i>,6<i>R</i>)-penexpandine.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"720 - 723"},"PeriodicalIF":0.9,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145167596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Mansurov, R. Rouzimaimaiti, S. Numonov, H. A. Aisa, Z. Bo
{"title":"Chemical Composition of the Etoac Fraction of Nepeta glutinosa Growing in Tajikistan","authors":"M. Mansurov, R. Rouzimaimaiti, S. Numonov, H. A. Aisa, Z. Bo","doi":"10.1007/s10600-025-04762-8","DOIUrl":"10.1007/s10600-025-04762-8","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"794 - 797"},"PeriodicalIF":0.9,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Y. J. Tseng, C. L. Kao, H. T. Li, S. T. Huang, M. J. Cheng, J. J. Wang, C. Y. Chen, W. J. Li
{"title":"Metabolites from Cordyceps sinensis with Antioxidant Activity","authors":"Y. J. Tseng, C. L. Kao, H. T. Li, S. T. Huang, M. J. Cheng, J. J. Wang, C. Y. Chen, W. J. Li","doi":"10.1007/s10600-025-04756-6","DOIUrl":"10.1007/s10600-025-04756-6","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"778 - 781"},"PeriodicalIF":0.9,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168034","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abubakar Siddiq Salihu, Wan Mohd Nuzul Hakimi Wan Salleh, Nurunajah Ab Ghani, Mohsen Gavahian
{"title":"Volatile Oil Components from the Leaves of Macaranga hullettii","authors":"Abubakar Siddiq Salihu, Wan Mohd Nuzul Hakimi Wan Salleh, Nurunajah Ab Ghani, Mohsen Gavahian","doi":"10.1007/s10600-025-04766-4","DOIUrl":"10.1007/s10600-025-04766-4","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"808 - 809"},"PeriodicalIF":0.9,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145160562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chung Yi Chen, Su Ting Huang, Hui Min David Wang, Su Ling Liu, Ming Jen Cheng, Hsing Tan Li
{"title":"Metabolites from Michelia alba with Antioxidant Activity","authors":"Chung Yi Chen, Su Ting Huang, Hui Min David Wang, Su Ling Liu, Ming Jen Cheng, Hsing Tan Li","doi":"10.1007/s10600-025-04739-7","DOIUrl":"10.1007/s10600-025-04739-7","url":null,"abstract":"<p>A new pyridine, 4-(2′-methylpropoxyl)-2-methylpyridine (<b>14</b>), as well as michelenolide, 11,13-dehydrolanuginolide, parthenolide, santamarine, dihydrosantamarine, (–)-anonaine, oxoxylopine, liriodenine, (–)-<i>N</i>-formylstepharine, scopoletin, coumarin, (3<i>S</i>,4<i>R</i>)-4-hydroxymellein, and (3<i>S</i>,4<i>S</i>)-4-hydroxymellein, were isolated from the stems of <i>Michelia alba</i>. The structure of the new pyridine was elucidated by chemical and physical evidence.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"698 - 701"},"PeriodicalIF":0.9,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. L. Yang, M. Y. Chen, S. T. Huang, M. J. Cheng, C. Y. Chen, H. T. Li
{"title":"Secondary Metabolites of Foeniculum vulgare","authors":"T. L. Yang, M. Y. Chen, S. T. Huang, M. J. Cheng, C. Y. Chen, H. T. Li","doi":"10.1007/s10600-025-04742-y","DOIUrl":"10.1007/s10600-025-04742-y","url":null,"abstract":"<p>A new pyridine, named 4-(2′-methylpropoxyl)pyridine-2-carboxylic acid (mengyunine) (<b>1</b>) as well as 1′-(7-methoxybenzo[<i>d</i>][1,3]dioxol-5-yl)butan-1′-ol (<b>2</b>), 4,7-dimethoxy-5-(propanoyl)benzo[<i>d</i>][1,3]dioxole (<b>3</b>), scopoletin (<b>4</b>), aesculetin dimethyl ester (<b>5</b>), xanthyletin (<b>6</b>), demethylluvangetin (<b>7</b>), chromenylacrylic acid (<b>8</b>), apigenin (<b>9</b>), luteolin (<b>10</b>), ferulic acid (<b>11</b>), methyl ferulate (<b>12</b>), methyl caffeate (<b>13</b>), 3′,4′,5′-trimethoxycinnamyl alcohol (<b>14</b>), methyl indole-3-carboxylate (<b>15</b>), picolinic acid (<b>16</b>), and 3-methylpicolinic acid (<b>17</b>), were isolated from the MeOH extract of the roots of <i>Foeniculum vulgare</i>. The structure of the new pyridine was elucidated by chemical and physical evidence.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"713 - 716"},"PeriodicalIF":0.9,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145168027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A New Bisbenzylisoquinoline Alkaloid Isolated from Nelumbinis Plumula","authors":"Dongge Wang, Wenjun Wei, Yu. Fu, Xiaojuan An, Jiarui Han, Suxiang Feng","doi":"10.1007/s10600-025-04740-0","DOIUrl":"10.1007/s10600-025-04740-0","url":null,"abstract":"<p>Five isoquinoline alkaloids were isolated from the extract of Nelumbinis Plumula, including a new bisbenzylisoquinoline alkaloid identified as 6′-demethyl-13′-O-methylisoliensinine. The structures of these compounds were elucidated using comprehensive spectroscopic analyses.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"702 - 704"},"PeriodicalIF":0.9,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145167565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. U. Zhuraev, Kh. M. Bobakulov, D. R. Siddikov, O. K. Askarova, E. Kh. Botirov, K. K. Turgunov, S. A. Sasmakov, B. Tashkhodzhaev
{"title":"Components of Roots of Perovskia angustifolia","authors":"M. U. Zhuraev, Kh. M. Bobakulov, D. R. Siddikov, O. K. Askarova, E. Kh. Botirov, K. K. Turgunov, S. A. Sasmakov, B. Tashkhodzhaev","doi":"10.1007/s10600-025-04757-5","DOIUrl":"10.1007/s10600-025-04757-5","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"773 - 777"},"PeriodicalIF":0.9,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145167562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chemical Constituents from the Branches and Leaves of Elaeagnus mollis and Screening of Anti-Liver Injury Activity","authors":"Ying Zhang, Hongfeng Quan, Jun Liu, Lin Dong","doi":"10.1007/s10600-025-04733-z","DOIUrl":"10.1007/s10600-025-04733-z","url":null,"abstract":"<p>In this research, 19 compounds were isolated from the leaves and branches of <i>Elaeagnus mollis</i> Diels. Of these, compound <b>1</b> was a new natural product, while compounds <b>2–11</b>, <b>13–19</b> were isolated for the first time from this genus. The isolated compounds were screened for hepatocyte proliferation and protective activity <i>in vitro</i>. Compounds <b>6–10</b>, <b>12</b>, and <b>18</b> exhibited both in vitro AML12 cell proliferation activity and protective activity against LPS-induced injury.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"666 - 672"},"PeriodicalIF":0.9,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145167558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}