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Chemistry of Natural Compounds最新文献

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Synthesis, Antiurease and Antioxidant Study of Two Novel Derivatives of Oleanolic Acid 齐墩果酸两种新型衍生物的合成、抗脲酶及抗氧化研究
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-13 DOI: 10.1007/s10600-026-05079-w
Nuzhat Arshad, Sadia Ansari, Anjum Ayub, Shumaila Jawaid, Jamshed Hashim, Maaz Bin Khalid, Zarish Alamgir
{"title":"Synthesis, Antiurease and Antioxidant Study of Two Novel Derivatives of Oleanolic Acid","authors":"Nuzhat Arshad, Sadia Ansari, Anjum Ayub, Shumaila Jawaid, Jamshed Hashim, Maaz Bin Khalid, Zarish Alamgir","doi":"10.1007/s10600-026-05079-w","DOIUrl":"10.1007/s10600-026-05079-w","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"840 - 842"},"PeriodicalIF":1.1,"publicationDate":"2026-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962309","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}
引用次数: 0
Isolation and Structural Characterization of Chemical Constituents from the Roots of Moringa oleifera 辣木根化学成分的分离与结构表征
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-13 DOI: 10.1007/s10600-026-05083-0
Yuya Ota, Tetsuya Saito, Yuria Kurosu, Takahiro Hosoya
{"title":"Isolation and Structural Characterization of Chemical Constituents from the Roots of Moringa oleifera","authors":"Yuya Ota,&nbsp;Tetsuya Saito,&nbsp;Yuria Kurosu,&nbsp;Takahiro Hosoya","doi":"10.1007/s10600-026-05083-0","DOIUrl":"10.1007/s10600-026-05083-0","url":null,"abstract":"<p>In this study, 14 compounds, including a novel pyrrole alkaloid glycoside (<b>6</b>), were isolated from <i>Moringa oleifera</i> roots, and their structures were determined using spectroscopic analyses. This is to our knowledge the first report of compounds <b>1</b>–<b>5</b>, <b>7</b>, and <b>10</b> isolated from <i>M. oleifera</i> roots, and compounds <b>8</b>, <b>9</b>, and <b>11</b>–<b>14</b> from the plant. Our findings highlight the chemical diversity of <i>M. oleifera</i> and provide novel insights into its chemical profile.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"772 - 777"},"PeriodicalIF":1.1,"publicationDate":"2026-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962195","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}
引用次数: 0
New Flavone Glycoside from the Aerial Part of Datisca cannabina and Its Antiradical Activity 大戟地部新黄酮苷及其抗自由基活性研究
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-13 DOI: 10.1007/s10600-026-05042-9
D. Sh. Akhmedova, A. A. Ganiev, Kh. M. Bobakulov, S. Z. Nishanbaev, D. A. Narbutaeva, N. D. Abdullaev, K. K. Turgunov
{"title":"New Flavone Glycoside from the Aerial Part of Datisca cannabina and Its Antiradical Activity","authors":"D. Sh. Akhmedova,&nbsp;A. A. Ganiev,&nbsp;Kh. M. Bobakulov,&nbsp;S. Z. Nishanbaev,&nbsp;D. A. Narbutaeva,&nbsp;N. D. Abdullaev,&nbsp;K. K. Turgunov","doi":"10.1007/s10600-026-05042-9","DOIUrl":"10.1007/s10600-026-05042-9","url":null,"abstract":"<p>The new flavone glycoside datiscetinoside (datiscetin-2′-O-β-D-glucopyranoside) (<b>1</b>) and ten known aglycon and glycosylated flavonoids (<b>2</b>–<b>11</b>) were isolated from the aerial part of <i>Datisca cannabina</i> (Datiscaceae). The chemical structures of the isolated compounds were proved and identified using IR, UV, <sup>1</sup>H and <sup>13</sup>C NMR spectra and COSY, HSQC, and HMBC experiments. The antiradical activity of total flavonoids obtained from the EtOAc fraction of the aqueous EtOH extract of the aerial part of <i>D. cannabina</i> was investigated.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"677 - 681"},"PeriodicalIF":1.1,"publicationDate":"2026-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962305","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}
引用次数: 0
Secondary Metabolites from the Grape Endophytic Aspergillus pseudodeflectus 葡萄内生假偏转曲霉的次生代谢物
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-12 DOI: 10.1007/s10600-026-05070-5
Chuan-Mao Zhang, Dong-Ping Li, Yu-Qin Yang, Jin-Feng Cao, Jian-Hai Ding
{"title":"Secondary Metabolites from the Grape Endophytic Aspergillus pseudodeflectus","authors":"Chuan-Mao Zhang,&nbsp;Dong-Ping Li,&nbsp;Yu-Qin Yang,&nbsp;Jin-Feng Cao,&nbsp;Jian-Hai Ding","doi":"10.1007/s10600-026-05070-5","DOIUrl":"10.1007/s10600-026-05070-5","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"811 - 813"},"PeriodicalIF":1.1,"publicationDate":"2026-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962136","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}
引用次数: 0
Secondary Metabolites of Hibiscus sabdariffa 木槿次生代谢物的研究
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-12 DOI: 10.1007/s10600-026-05064-3
P. H. Lee, M. J. Cheng, C. L. Kao, C. E. Kuo, S. T. Huang, H. T. Li, C. Y. Chen
{"title":"Secondary Metabolites of Hibiscus sabdariffa","authors":"P. H. Lee,&nbsp;M. J. Cheng,&nbsp;C. L. Kao,&nbsp;C. E. Kuo,&nbsp;S. T. Huang,&nbsp;H. T. Li,&nbsp;C. Y. Chen","doi":"10.1007/s10600-026-05064-3","DOIUrl":"10.1007/s10600-026-05064-3","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"792 - 795"},"PeriodicalIF":1.1,"publicationDate":"2026-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962137","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}
引用次数: 0
A New Apocarotenoid Glucoside of Synsepalum dulcificum 一种新的麻瓜类伪麻甙
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-12 DOI: 10.1007/s10600-026-05046-5
K. E. Chang, M. J. Cheng, C. L. Kao, S. T. Huang, C. Y. Chen, H. T. Li
{"title":"A New Apocarotenoid Glucoside of Synsepalum dulcificum","authors":"K. E. Chang,&nbsp;M. J. Cheng,&nbsp;C. L. Kao,&nbsp;S. T. Huang,&nbsp;C. Y. Chen,&nbsp;H. T. Li","doi":"10.1007/s10600-026-05046-5","DOIUrl":"10.1007/s10600-026-05046-5","url":null,"abstract":"<p>A new apocarotenoid glucoside, syndulcific acid (<b>1</b>) as well as (+)-vomifoliol (<b>2</b>), (+)-dehydrovomifoliol (<b>3</b>), 4-acetonyl-3,5-dimethoxy-p-quinol (<b>4</b>), protocatechuic alcohol (<b>5</b>), protocatechuic acid (<b>6</b>), malic acid (<b>7</b>), and 3-hydroxypropionic acid (<b>8</b>), were isolated from the fruits of <i>Synsepalum dulcificum</i> (Sapotaceae). The structure of the new apocarotenoid glucoside was elucidated by chemical and physical evidence.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"693 - 696"},"PeriodicalIF":1.1,"publicationDate":"2026-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962133","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}
引用次数: 0
Phenolic Compounds from Artemisia porrecta 茯苓中的酚类化合物
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-12 DOI: 10.1007/s10600-026-05071-4
O. A. Abdullajanov, A. A. Ganiev, N. B. Begmatov, Kh. M. Bobakulov, G. Mamajanov, J. Zhao, F. He, Sh. V. Abdullaev, I. Askarov, Kh. Bozorov, A. Turak
{"title":"Phenolic Compounds from Artemisia porrecta","authors":"O. A. Abdullajanov,&nbsp;A. A. Ganiev,&nbsp;N. B. Begmatov,&nbsp;Kh. M. Bobakulov,&nbsp;G. Mamajanov,&nbsp;J. Zhao,&nbsp;F. He,&nbsp;Sh. V. Abdullaev,&nbsp;I. Askarov,&nbsp;Kh. Bozorov,&nbsp;A. Turak","doi":"10.1007/s10600-026-05071-4","DOIUrl":"10.1007/s10600-026-05071-4","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"814 - 816"},"PeriodicalIF":1.1,"publicationDate":"2026-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962135","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}
引用次数: 0
Secondary Metabolites of Castanea mollissima 板栗的次生代谢物
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-12 DOI: 10.1007/s10600-026-05066-1
P. H. Lee, M. J. Cheng, C. L. Kao, C. E. Kuo, S. T. Huang, H. T. Li, C. Y. Chen
{"title":"Secondary Metabolites of Castanea mollissima","authors":"P. H. Lee,&nbsp;M. J. Cheng,&nbsp;C. L. Kao,&nbsp;C. E. Kuo,&nbsp;S. T. Huang,&nbsp;H. T. Li,&nbsp;C. Y. Chen","doi":"10.1007/s10600-026-05066-1","DOIUrl":"10.1007/s10600-026-05066-1","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"799 - 802"},"PeriodicalIF":1.1,"publicationDate":"2026-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148962138","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}
引用次数: 0
Chemical Constituents of Cydonia oblonga and Their Anti-Inflammatory Activity Cydonia oblonga的化学成分及其抗炎活性
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-11 DOI: 10.1007/s10600-026-05069-y
Y. Zhou, C. Liu, Z. Li, Y. Yuan, J. Zhao, H. A. Aisa
{"title":"Chemical Constituents of Cydonia oblonga and Their Anti-Inflammatory Activity","authors":"Y. Zhou,&nbsp;C. Liu,&nbsp;Z. Li,&nbsp;Y. Yuan,&nbsp;J. Zhao,&nbsp;H. A. Aisa","doi":"10.1007/s10600-026-05069-y","DOIUrl":"10.1007/s10600-026-05069-y","url":null,"abstract":"","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"808 - 810"},"PeriodicalIF":1.1,"publicationDate":"2026-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148961909","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}
引用次数: 0
Synthetic Transformations of Higher Terpenoids. 48. Synthesis and Cytotoxic Properties of 18-Nor-Labdatriene-Containing Ureas 高等萜类化合物的合成转化。含18- no - labdatri烯脲的合成及细胞毒性研究
IF 1.1 4区 化学
Chemistry of Natural Compounds Pub Date : 2026-08-11 DOI: 10.1007/s10600-026-05055-4
Yu. V. Kharitonov, V. I. Antipova, M. K. Marenina, Yu. V. Meshkova, T. G. Tolstikova, E. E. Shults
{"title":"Synthetic Transformations of Higher Terpenoids. 48. Synthesis and Cytotoxic Properties of 18-Nor-Labdatriene-Containing Ureas","authors":"Yu. V. Kharitonov,&nbsp;V. I. Antipova,&nbsp;M. K. Marenina,&nbsp;Yu. V. Meshkova,&nbsp;T. G. Tolstikova,&nbsp;E. E. Shults","doi":"10.1007/s10600-026-05055-4","DOIUrl":"10.1007/s10600-026-05055-4","url":null,"abstract":"<p>A series of 4-ureido-18-nor-15,16-epoxy-8(17),13,14-labdatrienes were synthesized by the reaction of 4-isocyanato-18-nor-lambertianic acid with ammonia, primary and secondary amines, amino acids, and phenylamines. The reactions occurred under mild conditions with high yields of the target products. The cytotoxicity of the synthesized compounds was assessed against cultivated human tumor cells MCF-7 and HEK293T and fibroblasts hTERT-BJ1 (MTT assay). Hierarchical clustering was used for qualitative analysis of the structure–cytotoxicity relationship and revealed several patterns for the effect of the substituent nature on the cytotoxicity and selectivity. The highest selectivity against tumor cells (SI = 2.2–2.3) was found for <b>3</b>, <b>5e</b>, and <b>11b</b>.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"62 4","pages":"736 - 746"},"PeriodicalIF":1.1,"publicationDate":"2026-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148961908","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}
引用次数: 0
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