Kh. N. Olimova, U. Kh. Kurbanov, R. Ya. Okmanov, B. Tashkhodzhaev, N. I. Mukarramov, S. M. Turaeva
{"title":"Pyrrolizidine Alkaloids from Heliotropium lasiocarpum and Insecticidal Activity of Their Extracts","authors":"Kh. N. Olimova, U. Kh. Kurbanov, R. Ya. Okmanov, B. Tashkhodzhaev, N. I. Mukarramov, S. M. Turaeva","doi":"10.1007/s10600-025-04748-6","DOIUrl":null,"url":null,"abstract":"<p>The new pyrrolizidine alkaloid helasine (<b>1</b>) and known heliotrine (<b>2</b>), lasiocarpine N-oxide (<b>3</b>), trachelanthamine (<b>4</b>), and echinatine (<b>5</b>) were isolated from the plant Heliotropium lasiocarpum. Alkaloids <b>4</b> and <b>5</b> were observed for the first time in H. lasiocarpum. The absolute configurations of isolated alkaloids <b>2</b>–<b>4</b> were established by X-ray crystal structure analyses. The insecticidal activity of the CHCl<sub>3</sub>, n-BuOH, and H<sub>2</sub>O parts of the H. lasiocarpum extract against Callosobruchus maculates and Sitophilus oryzae was examined. The CHCl<sub>3</sub> extract at a dose of 10 mg/L had the highest activity.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"748 - 754"},"PeriodicalIF":0.9000,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04748-6","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
The new pyrrolizidine alkaloid helasine (1) and known heliotrine (2), lasiocarpine N-oxide (3), trachelanthamine (4), and echinatine (5) were isolated from the plant Heliotropium lasiocarpum. Alkaloids 4 and 5 were observed for the first time in H. lasiocarpum. The absolute configurations of isolated alkaloids 2–4 were established by X-ray crystal structure analyses. The insecticidal activity of the CHCl3, n-BuOH, and H2O parts of the H. lasiocarpum extract against Callosobruchus maculates and Sitophilus oryzae was examined. The CHCl3 extract at a dose of 10 mg/L had the highest activity.
期刊介绍:
Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.