Shan-Shan Liu , Yun Li , Yun-He An , Jing-Jing Zhu , Mei Zhang , Wei Wang , Li-Hua Yan , Zhi-Min Wang
{"title":"泽泻的倍半萜对映体。","authors":"Shan-Shan Liu , Yun Li , Yun-He An , Jing-Jing Zhu , Mei Zhang , Wei Wang , Li-Hua Yan , Zhi-Min Wang","doi":"10.1016/j.phytochem.2024.114359","DOIUrl":null,"url":null,"abstract":"<div><div>A pair of dinor-sesquiterpene enantiomers (<strong>1a/1b</strong>), eight pairs of guaiane-type sesquiterpenes enantiomers (<strong>2a/2b, 3a/3b, 4a/4b, 5a/5b, 6a/6b, 7a/7b, 8a/8b, 9a/9b</strong>) and two guaiane-type sesquiterpenes (<strong>10, 11</strong>), including eleven undescribed ones (<strong>1a, 1b, 2a, 2b, 3a, 3b, 4a, 5b, 6a, 10,</strong> and <strong>11</strong>), were isolated from the aqueous extract of Alismatis Rhizoma. The structures were elucidated by combining 1D and 2D NMR and HRESIMS spectroscopic data. The absolute configurations were determined by experimental and calculated ECD spectra, [Mo<sub>2</sub>(OAc)<sub>4</sub>]-induced ECD spectral analysis, and comparison of the experimental ECD spectra with those of similar analogs. Compound <strong>5b</strong> (NO inhibition rate, 52.63%) and <strong>8b</strong> (36.49%) showed comparable activity to indomethacin (46.36%) against LPS-induced NO production in RAW 264.7 murine macrophages at 100 μM with obvious stereoselectivity, whereas compounds <strong>1</strong>–<strong>10</strong> exerted no or extremely low cytotoxicities against MCF-7 and MDA-MB-231 cells (IC<sub>50</sub> > 100 μM).</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"232 ","pages":"Article 114359"},"PeriodicalIF":3.2000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sesquiterpene enantiomers from Alismatis Rhizoma\",\"authors\":\"Shan-Shan Liu , Yun Li , Yun-He An , Jing-Jing Zhu , Mei Zhang , Wei Wang , Li-Hua Yan , Zhi-Min Wang\",\"doi\":\"10.1016/j.phytochem.2024.114359\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A pair of dinor-sesquiterpene enantiomers (<strong>1a/1b</strong>), eight pairs of guaiane-type sesquiterpenes enantiomers (<strong>2a/2b, 3a/3b, 4a/4b, 5a/5b, 6a/6b, 7a/7b, 8a/8b, 9a/9b</strong>) and two guaiane-type sesquiterpenes (<strong>10, 11</strong>), including eleven undescribed ones (<strong>1a, 1b, 2a, 2b, 3a, 3b, 4a, 5b, 6a, 10,</strong> and <strong>11</strong>), were isolated from the aqueous extract of Alismatis Rhizoma. The structures were elucidated by combining 1D and 2D NMR and HRESIMS spectroscopic data. The absolute configurations were determined by experimental and calculated ECD spectra, [Mo<sub>2</sub>(OAc)<sub>4</sub>]-induced ECD spectral analysis, and comparison of the experimental ECD spectra with those of similar analogs. Compound <strong>5b</strong> (NO inhibition rate, 52.63%) and <strong>8b</strong> (36.49%) showed comparable activity to indomethacin (46.36%) against LPS-induced NO production in RAW 264.7 murine macrophages at 100 μM with obvious stereoselectivity, whereas compounds <strong>1</strong>–<strong>10</strong> exerted no or extremely low cytotoxicities against MCF-7 and MDA-MB-231 cells (IC<sub>50</sub> > 100 μM).</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"232 \",\"pages\":\"Article 114359\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-12-12\",\"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/S0031942224003960\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942224003960","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}
A pair of dinor-sesquiterpene enantiomers (1a/1b), eight pairs of guaiane-type sesquiterpenes enantiomers (2a/2b, 3a/3b, 4a/4b, 5a/5b, 6a/6b, 7a/7b, 8a/8b, 9a/9b) and two guaiane-type sesquiterpenes (10, 11), including eleven undescribed ones (1a, 1b, 2a, 2b, 3a, 3b, 4a, 5b, 6a, 10, and 11), were isolated from the aqueous extract of Alismatis Rhizoma. The structures were elucidated by combining 1D and 2D NMR and HRESIMS spectroscopic data. The absolute configurations were determined by experimental and calculated ECD spectra, [Mo2(OAc)4]-induced ECD spectral analysis, and comparison of the experimental ECD spectra with those of similar analogs. Compound 5b (NO inhibition rate, 52.63%) and 8b (36.49%) showed comparable activity to indomethacin (46.36%) against LPS-induced NO production in RAW 264.7 murine macrophages at 100 μM with obvious stereoselectivity, whereas compounds 1–10 exerted no or extremely low cytotoxicities against MCF-7 and MDA-MB-231 cells (IC50 > 100 μM).
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.