{"title":"Hendersines J–M: Isoquinoline alkaloids from Corydalis hendersonii Hemsl. with cardiomyocyte protective and NO production inhibitory effects","authors":"Xiaochun Zhou , Zefeng Zhang , Changxin Liu , Shungang Jiao , Fuxing Ge , Qiuyuan Ding , Yiru Shen , Qiang Guo , Xingyun Chai","doi":"10.1016/j.phytochem.2024.114365","DOIUrl":null,"url":null,"abstract":"<div><div>Six isoquinoline alkaloids were identified from the alkaloid-rich fraction of <em>Corydalis hendersonii</em> Hemsl, including five previously undescribed isoquinoline alkaloids hendersines J–M (<strong>1a</strong>, <strong>1b</strong>, and <strong>2</strong>–<strong>4</strong>) and isobicuculline (<strong>5</strong>), a compound reported for the first time from a natural source. Their structures were elucidated based on spectroscopic analysis of HR-ESI-MS, 1D and 2D NMR, X-ray diffraction, and ECD. Compounds <strong>1a</strong> and <strong>1b</strong> represent a pair of rare three-nitrogen isoquinoline alkaloid enantiomers, while <strong>2</strong> and <strong>3</strong> are isoquinoline alkaloids featuring a benzo-fused <em>N</em>-heterocycle. Compounds <strong>1a</strong> and <strong>3</strong> exhibited moderate protective effects against oxygen-glucose deprivation-induced H9c2 cells injury, <strong>1b</strong> and <strong>2</strong> showed moderate inhibitory effects on NO production in lipopolysaccharide-induced RAW264.7 cells.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"232 ","pages":"Article 114365"},"PeriodicalIF":3.2000,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942224004023","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Six isoquinoline alkaloids were identified from the alkaloid-rich fraction of Corydalis hendersonii Hemsl, including five previously undescribed isoquinoline alkaloids hendersines J–M (1a, 1b, and 2–4) and isobicuculline (5), a compound reported for the first time from a natural source. Their structures were elucidated based on spectroscopic analysis of HR-ESI-MS, 1D and 2D NMR, X-ray diffraction, and ECD. Compounds 1a and 1b represent a pair of rare three-nitrogen isoquinoline alkaloid enantiomers, while 2 and 3 are isoquinoline alkaloids featuring a benzo-fused N-heterocycle. Compounds 1a and 3 exhibited moderate protective effects against oxygen-glucose deprivation-induced H9c2 cells injury, 1b and 2 showed moderate inhibitory effects on NO production in lipopolysaccharide-induced RAW264.7 cells.
期刊介绍:
Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.