Ting-Yu Cheng , Chia-Jung Yang , Po-Jen Chen , Yu-Li Chen , Bo-Rong Peng , Te-An Kung , Zhi-Hong Wen , Kuei-Hung Lai , Hsu-Ming Chung
{"title":"从软珊瑚 Capnella imbricata 中分离出的新类固醇 Capnesterones A 和 B","authors":"Ting-Yu Cheng , Chia-Jung Yang , Po-Jen Chen , Yu-Li Chen , Bo-Rong Peng , Te-An Kung , Zhi-Hong Wen , Kuei-Hung Lai , Hsu-Ming Chung","doi":"10.1016/j.phytol.2024.03.015","DOIUrl":null,"url":null,"abstract":"<div><p>Two new non-withanolidal steroids with a cross-conjugated dienone structural unit in ring A, capnesterones A (<strong>1</strong>) and B (<strong>2</strong>), were isolated from the soft coral <em>Capnella imbricata</em> in the southeast waters of Taiwan. The compounds' structures were elucidated through a comprehensive analysis of spectroscopic data, including IR, ESIMS, <sup>1</sup>H NMR, and <sup>13</sup>C NMR, and through comparison with previous literature. At a concentration of 10 μM, steroids <strong>1</strong> and <strong>2</strong> exhibited reductions in iNOS levels (60 % and 82 %) compared to LPS-stimulated control cells, along with increased release (134 % and 110 %) against COX-2 protein expressions.</p></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"61 ","pages":"Pages 115-119"},"PeriodicalIF":1.3000,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Capnesterones A and B, new steroids isolated from the soft coral Capnella imbricata\",\"authors\":\"Ting-Yu Cheng , Chia-Jung Yang , Po-Jen Chen , Yu-Li Chen , Bo-Rong Peng , Te-An Kung , Zhi-Hong Wen , Kuei-Hung Lai , Hsu-Ming Chung\",\"doi\":\"10.1016/j.phytol.2024.03.015\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Two new non-withanolidal steroids with a cross-conjugated dienone structural unit in ring A, capnesterones A (<strong>1</strong>) and B (<strong>2</strong>), were isolated from the soft coral <em>Capnella imbricata</em> in the southeast waters of Taiwan. The compounds' structures were elucidated through a comprehensive analysis of spectroscopic data, including IR, ESIMS, <sup>1</sup>H NMR, and <sup>13</sup>C NMR, and through comparison with previous literature. At a concentration of 10 μM, steroids <strong>1</strong> and <strong>2</strong> exhibited reductions in iNOS levels (60 % and 82 %) compared to LPS-stimulated control cells, along with increased release (134 % and 110 %) against COX-2 protein expressions.</p></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"61 \",\"pages\":\"Pages 115-119\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-04-12\",\"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/S1874390024000521\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1874390024000521","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Capnesterones A and B, new steroids isolated from the soft coral Capnella imbricata
Two new non-withanolidal steroids with a cross-conjugated dienone structural unit in ring A, capnesterones A (1) and B (2), were isolated from the soft coral Capnella imbricata in the southeast waters of Taiwan. The compounds' structures were elucidated through a comprehensive analysis of spectroscopic data, including IR, ESIMS, 1H NMR, and 13C NMR, and through comparison with previous literature. At a concentration of 10 μM, steroids 1 and 2 exhibited reductions in iNOS levels (60 % and 82 %) compared to LPS-stimulated control cells, along with increased release (134 % and 110 %) against COX-2 protein expressions.
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.