{"title":"New yellow pigments related to the pitholides from the Endophyte Sordariomycetes sp.","authors":"Kousei Shimizu , Reo Takahashi , Zulfikar , Mayuka Hakozaki , Yuko Kanno , Shota Uesugi , Takuya Koseki , Yoshihito Shiono","doi":"10.1016/j.phytol.2024.11.008","DOIUrl":null,"url":null,"abstract":"<div><div>Two novel yellow pigments, 7,8-dihydro-12-<em>O</em>-methylpitholide B (<strong>1</strong>) and 12-<em>O</em>-methylpitholide B (<strong>2</strong>), and two known compounds, pitholide B (<strong>3</strong>) and anishidiol (<strong>4</strong>), were isolated from an endophytic strain of <em>Sordariomycetes</em> sp. S-3. The structures of the new compounds, including their absolute configurations, were elucidated by nuclear magnetic resonance, infrared, ultraviolet, mass spectrometry, and electrochemical detection. The cytotoxicity and antimicrobial activities of the isolated compounds were also evaluated. Compound <strong>1</strong> exhibited cytotoxicity against HL60 cells with an IC<sub>50</sub> of 15.8 <em>μ</em>M, whereas compound <strong>3</strong> exhibited moderate cytotoxicity. Compound 3 inhibited <em>B. subtilis</em> at 50 <em>µ</em>g/disk, and <strong>4</strong> inhibited <em>Candida tropicalis</em>, <em>B. subtilis</em>, and <em>Aspergillus niger</em> at 50 µg/disk.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"65 ","pages":"Pages 10-14"},"PeriodicalIF":1.3000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S187439002400154X","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Two novel yellow pigments, 7,8-dihydro-12-O-methylpitholide B (1) and 12-O-methylpitholide B (2), and two known compounds, pitholide B (3) and anishidiol (4), were isolated from an endophytic strain of Sordariomycetes sp. S-3. The structures of the new compounds, including their absolute configurations, were elucidated by nuclear magnetic resonance, infrared, ultraviolet, mass spectrometry, and electrochemical detection. The cytotoxicity and antimicrobial activities of the isolated compounds were also evaluated. Compound 1 exhibited cytotoxicity against HL60 cells with an IC50 of 15.8 μM, whereas compound 3 exhibited moderate cytotoxicity. Compound 3 inhibited B. subtilis at 50 µg/disk, and 4 inhibited Candida tropicalis, B. subtilis, and Aspergillus niger at 50 µg/disk.
期刊介绍:
Phytochemistry Letters invites rapid communications on all aspects of natural product research including:
• Structural elucidation of natural products
• Analytical evaluation of herbal medicines
• Clinical efficacy, safety and pharmacovigilance of herbal medicines
• Natural product biosynthesis
• Natural product synthesis and chemical modification
• Natural product metabolism
• Chemical ecology
• Biotechnology
• Bioassay-guided isolation
• Pharmacognosy
• Pharmacology of natural products
• Metabolomics
• Ethnobotany and traditional usage
• Genetics of natural products
Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.