Matthieu Matcheme , Bernard Dabolé , Djaouda Moussa , Jean Noël Nyemb , Talla Emmanuel , Sophie Laurent , Céline Henoumont , Alessandro Venditti
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(Boraginaceae) resulted in the isolation of the following ten known compounds: 1-naphthaleneacetic-5-carboxy-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a-trimethyl-[1<em>S</em>-(1<em>α</em>,2<em>β</em>, 4a,8a<em>α</em>)]-acid (<strong>1</strong>), hexacosanoate-1-glyceryl (<strong>2</strong>), 3<em>β</em>-urs-12,20(30)-diene-27,28-dioic acid (<strong>3</strong>), 3<em>β</em>-D-glucopyranosylurs-12,20(30)-diene-27,28-dioic acid (<strong>4</strong>), stigmasterol (<strong>5</strong>), stigmasterol-3-<em>O</em>-<em>β</em>-D-glucopyranoside (<strong>6</strong>), oleanolic-acid (<strong>7</strong>), 3-<em>O</em>-acetyl-oleanolic acid (<strong>8</strong>), betulin (<strong>9</strong>) and spinasterol-3<em>β</em>-<em>O</em>-D-glucopyranoside (<strong>10</strong>). The isolated compounds were characterised by using spectroscopic methods, 1D and 2D NMR, mass spectroscopy (ESI-MS) and by comparison with the literature data. To the best of our knowledge, compounds <strong>1</strong>, <strong>3</strong>, <strong>4</strong>, <strong>8</strong> and <strong>10</strong> were isolated for the first time from the <em>Cordia</em> genus. This result improves the chemotaxonomy knowledge of the <em>Cordia</em> genus. The antibacterial activities were performed by the Muller–Hinton agar diffusion method. The antibacterial activities were studied on <em>Salmonella typhi</em>, <em>Staphylococcus aureus</em>, <em>Vibrio cholerae</em>, <em>Pseudomonas aeruginosa</em> and <em>Escherichia coli</em> ATCC 25922. Compounds <strong>8</strong> and <strong>9</strong>, at 20.0 mg/mL resulted to be effective antimicrobial against <em>E. coli</em>, <em>V. cholerae</em> and <em>P. aeruginosa.</em></div></div>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":"39 4","pages":"Pages 725-733"},"PeriodicalIF":1.9000,"publicationDate":"2025-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chemical constituents from Cordia myxa L. (Boraginaceae) and their antibacterial activity\",\"authors\":\"Matthieu Matcheme , Bernard Dabolé , Djaouda Moussa , Jean Noël Nyemb , Talla Emmanuel , Sophie Laurent , Céline Henoumont , Alessandro Venditti\",\"doi\":\"10.1080/14786419.2023.2288928\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Chemical investigation of <em>Cordia myxa</em> L. (Boraginaceae) resulted in the isolation of the following ten known compounds: 1-naphthaleneacetic-5-carboxy-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a-trimethyl-[1<em>S</em>-(1<em>α</em>,2<em>β</em>, 4a,8a<em>α</em>)]-acid (<strong>1</strong>), hexacosanoate-1-glyceryl (<strong>2</strong>), 3<em>β</em>-urs-12,20(30)-diene-27,28-dioic acid (<strong>3</strong>), 3<em>β</em>-D-glucopyranosylurs-12,20(30)-diene-27,28-dioic acid (<strong>4</strong>), stigmasterol (<strong>5</strong>), stigmasterol-3-<em>O</em>-<em>β</em>-D-glucopyranoside (<strong>6</strong>), oleanolic-acid (<strong>7</strong>), 3-<em>O</em>-acetyl-oleanolic acid (<strong>8</strong>), betulin (<strong>9</strong>) and spinasterol-3<em>β</em>-<em>O</em>-D-glucopyranoside (<strong>10</strong>). The isolated compounds were characterised by using spectroscopic methods, 1D and 2D NMR, mass spectroscopy (ESI-MS) and by comparison with the literature data. 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引用次数: 0
摘要
从菖蒲科菖蒲草中分离到10个已知化合物:1-萘乙酸-5-羧基-1,2,3,4,4a,7,8,8 -a -八氢-1,2,4 -三甲基-[1S-(1α,2β, 4a,8aα)]-酸(1),己糖酸-1-甘油三酯(2),3- β- 12,20(30)-二烯-27,28-二烯酸(3),3- β- d -葡萄糖吡喃基-12,20(30)-二烯-27,28-二烯酸(4),豆甾醇(5),豆甾醇-3- o- β- d -葡萄糖吡喃苷(6),齐墩果酸(7),3- o-乙酰齐墩果酸(8),桦木素(9)和spinasterol-3 -β- o- d -葡萄糖吡喃苷(10)。通过波谱方法、一维和二维核磁共振、质谱(ESI-MS)以及与文献数据的比较,对分离得到的化合物进行了表征。化合物1、3、4、8和10为首次从该属植物中分离得到。这一结果提高了科迪亚属植物的化学分类学知识。采用Muller-Hinton琼脂扩散法测定其抑菌活性。研究了其对伤寒沙门氏菌、金黄色葡萄球菌、霍乱弧菌、铜绿假单胞菌和大肠埃希菌的抑菌活性。化合物8和9在20.0 mg/mL浓度下对大肠杆菌、霍乱弧菌和铜绿假单胞菌均有较好的抗菌作用。
Chemical constituents from Cordia myxa L. (Boraginaceae) and their antibacterial activity
Chemical investigation of Cordia myxa L. (Boraginaceae) resulted in the isolation of the following ten known compounds: 1-naphthaleneacetic-5-carboxy-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a-trimethyl-[1S-(1α,2β, 4a,8aα)]-acid (1), hexacosanoate-1-glyceryl (2), 3β-urs-12,20(30)-diene-27,28-dioic acid (3), 3β-D-glucopyranosylurs-12,20(30)-diene-27,28-dioic acid (4), stigmasterol (5), stigmasterol-3-O-β-D-glucopyranoside (6), oleanolic-acid (7), 3-O-acetyl-oleanolic acid (8), betulin (9) and spinasterol-3β-O-D-glucopyranoside (10). The isolated compounds were characterised by using spectroscopic methods, 1D and 2D NMR, mass spectroscopy (ESI-MS) and by comparison with the literature data. To the best of our knowledge, compounds 1, 3, 4, 8 and 10 were isolated for the first time from the Cordia genus. This result improves the chemotaxonomy knowledge of the Cordia genus. The antibacterial activities were performed by the Muller–Hinton agar diffusion method. The antibacterial activities were studied on Salmonella typhi, Staphylococcus aureus, Vibrio cholerae, Pseudomonas aeruginosa and Escherichia coli ATCC 25922. Compounds 8 and 9, at 20.0 mg/mL resulted to be effective antimicrobial against E. coli, V. cholerae and P. aeruginosa.
期刊介绍:
The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds.
The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal.
Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section.
All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.