{"title":"来自金钗石斛的 Isosativene 和 sativene 倍半萜衍生物。","authors":"","doi":"10.1016/j.fitote.2024.106281","DOIUrl":null,"url":null,"abstract":"<div><div>Two unusual isosativene sesquiterpene derivatives, named dendronobilol A (<strong>1</strong>) and dendronobilside A (<strong>2</strong>), and two unusual sativene sesquiterpene derivatives, named dendronobilsides B (<strong>3</strong>) and C (<strong>4</strong>), had been isolated from the stems of <em>Dendrobium nobile</em>. The structures of all the compounds were established using spectroscopic methods and by comparison with literature data, and their absolute configurations were confirmed via single-crystal X-ray diffraction data and electronic circular dichroism (ECD) calculations. Dendronobilol A (<strong>1</strong>) and dendronobilside A (<strong>2</strong>) possessed a unique tricyclo[4.3.0.1<sup>2, 8</sup>]decan ring system, while dendronobilsides B (<strong>3</strong>) and C (<strong>4</strong>) presented a unique tricyclo[4.4.0.0<sup>2, 8</sup>]decan core carbon skeleton. The above two types of sesquiterpene derivatives had been isolated and purified from plants for the first time. Compounds <strong>1</strong> and <strong>2</strong> exhibited significant effects on glucose consumption with doses of 20 and 40 μmol/L in insulin-resistant HepG2 cells, and thus improve insulin resistance.</div></div>","PeriodicalId":12147,"journal":{"name":"Fitoterapia","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isosativene and sativene sesquiterpene derivatives from Dendrobium nobile\",\"authors\":\"\",\"doi\":\"10.1016/j.fitote.2024.106281\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Two unusual isosativene sesquiterpene derivatives, named dendronobilol A (<strong>1</strong>) and dendronobilside A (<strong>2</strong>), and two unusual sativene sesquiterpene derivatives, named dendronobilsides B (<strong>3</strong>) and C (<strong>4</strong>), had been isolated from the stems of <em>Dendrobium nobile</em>. The structures of all the compounds were established using spectroscopic methods and by comparison with literature data, and their absolute configurations were confirmed via single-crystal X-ray diffraction data and electronic circular dichroism (ECD) calculations. Dendronobilol A (<strong>1</strong>) and dendronobilside A (<strong>2</strong>) possessed a unique tricyclo[4.3.0.1<sup>2, 8</sup>]decan ring system, while dendronobilsides B (<strong>3</strong>) and C (<strong>4</strong>) presented a unique tricyclo[4.4.0.0<sup>2, 8</sup>]decan core carbon skeleton. The above two types of sesquiterpene derivatives had been isolated and purified from plants for the first time. Compounds <strong>1</strong> and <strong>2</strong> exhibited significant effects on glucose consumption with doses of 20 and 40 μmol/L in insulin-resistant HepG2 cells, and thus improve insulin resistance.</div></div>\",\"PeriodicalId\":12147,\"journal\":{\"name\":\"Fitoterapia\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fitoterapia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0367326X24004647\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fitoterapia","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0367326X24004647","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
摘要
从金钗石斛的茎中分离出了两种不同寻常的异亚梓倍半萜衍生物,分别命名为树枝烯醇 A (1) 和树枝烯侧 A (2),以及两种不同寻常的亚梓倍半萜衍生物,分别命名为树枝烯侧 B (3) 和树枝烯侧 C (4)。通过光谱方法以及与文献数据的比较,确定了所有化合物的结构,并通过单晶 X 射线衍射数据和电子圆二色性(ECD)计算确认了它们的绝对构型。Dendronobilol A (1) 和 dendronobilside A (2) 具有独特的三环[4.3.0.12, 8]癸烷环系统,而 dendronobilsides B (3) 和 C (4) 则呈现独特的三环[4.4.0.02, 8]癸烷核心碳骨架。上述两种倍半萜衍生物是首次从植物中分离和纯化出来的。化合物 1 和 2 对胰岛素抵抗的 HepG2 细胞的葡萄糖消耗有显著影响,剂量分别为 20 和 40 μmol/L,从而改善了胰岛素抵抗。
Isosativene and sativene sesquiterpene derivatives from Dendrobium nobile
Two unusual isosativene sesquiterpene derivatives, named dendronobilol A (1) and dendronobilside A (2), and two unusual sativene sesquiterpene derivatives, named dendronobilsides B (3) and C (4), had been isolated from the stems of Dendrobium nobile. The structures of all the compounds were established using spectroscopic methods and by comparison with literature data, and their absolute configurations were confirmed via single-crystal X-ray diffraction data and electronic circular dichroism (ECD) calculations. Dendronobilol A (1) and dendronobilside A (2) possessed a unique tricyclo[4.3.0.12, 8]decan ring system, while dendronobilsides B (3) and C (4) presented a unique tricyclo[4.4.0.02, 8]decan core carbon skeleton. The above two types of sesquiterpene derivatives had been isolated and purified from plants for the first time. Compounds 1 and 2 exhibited significant effects on glucose consumption with doses of 20 and 40 μmol/L in insulin-resistant HepG2 cells, and thus improve insulin resistance.
期刊介绍:
Fitoterapia is a Journal dedicated to medicinal plants and to bioactive natural products of plant origin. It publishes original contributions in seven major areas:
1. Characterization of active ingredients of medicinal plants
2. Development of standardization method for bioactive plant extracts and natural products
3. Identification of bioactivity in plant extracts
4. Identification of targets and mechanism of activity of plant extracts
5. Production and genomic characterization of medicinal plants biomass
6. Chemistry and biochemistry of bioactive natural products of plant origin
7. Critical reviews of the historical, clinical and legal status of medicinal plants, and accounts on topical issues.