Yikao Hu , Wen Xu , Li Wang , Yuanbiao He , Yong Zhao
{"title":"具有显著α-葡萄糖苷酶抑制活性的翅果茜草酸衍生物","authors":"Yikao Hu , Wen Xu , Li Wang , Yuanbiao He , Yong Zhao","doi":"10.1016/j.phytol.2024.03.016","DOIUrl":null,"url":null,"abstract":"<div><p>Our continuous effort to search for antidiabetic constituents from the leaves of <em>Syzygium samarangense</em> resulted in the isolation of one new anacardic acid derivative, 2-[(<em>Z</em>)-nonadec-14-enyl]-6-hydroxylbenzoic acid (<strong>1</strong>) along with four known analogues (<strong>2</strong>−<strong>5</strong>). The new structure was elucidated by means of extensive spectroscopic data including 1D and 2D NMR along with HRESIMS. The anacardic acid derivatives were isolated from this species for the first time<em>.</em> All compounds exhibited significant inhibitory effect with IC<sub>50</sub> value of 0.75−3.60 μM against <em>α</em>-glucosidase.</p></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"61 ","pages":"Pages 75-77"},"PeriodicalIF":1.3000,"publicationDate":"2024-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anacardic acid derivatives with significant α-glucosidase inhibitory activity from Syzygium samarangense\",\"authors\":\"Yikao Hu , Wen Xu , Li Wang , Yuanbiao He , Yong Zhao\",\"doi\":\"10.1016/j.phytol.2024.03.016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Our continuous effort to search for antidiabetic constituents from the leaves of <em>Syzygium samarangense</em> resulted in the isolation of one new anacardic acid derivative, 2-[(<em>Z</em>)-nonadec-14-enyl]-6-hydroxylbenzoic acid (<strong>1</strong>) along with four known analogues (<strong>2</strong>−<strong>5</strong>). The new structure was elucidated by means of extensive spectroscopic data including 1D and 2D NMR along with HRESIMS. The anacardic acid derivatives were isolated from this species for the first time<em>.</em> All compounds exhibited significant inhibitory effect with IC<sub>50</sub> value of 0.75−3.60 μM against <em>α</em>-glucosidase.</p></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"61 \",\"pages\":\"Pages 75-77\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-03-30\",\"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/S1874390024000557\",\"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/S1874390024000557","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Anacardic acid derivatives with significant α-glucosidase inhibitory activity from Syzygium samarangense
Our continuous effort to search for antidiabetic constituents from the leaves of Syzygium samarangense resulted in the isolation of one new anacardic acid derivative, 2-[(Z)-nonadec-14-enyl]-6-hydroxylbenzoic acid (1) along with four known analogues (2−5). The new structure was elucidated by means of extensive spectroscopic data including 1D and 2D NMR along with HRESIMS. The anacardic acid derivatives were isolated from this species for the first time. All compounds exhibited significant inhibitory effect with IC50 value of 0.75−3.60 μM against α-glucosidase.
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.