{"title":"Two new bergamotane-type sesquiterpeniods from the plant endophytic fungus <i>Paraconiothyrium brasiliense</i>.","authors":"Ying Shi, Ling Liu","doi":"10.1080/10286020.2025.2477631","DOIUrl":null,"url":null,"abstract":"<p><p>One new bergamotane-type sesquiterpeniod lactam brasilactam A (<b>1</b>) and one new bergamotane-type sesquiterpeniod spiroketal lactone brasiketalolide A (<b>2</b>), along with two known compounds ampullicin (<b>3</b>) and isoampullicin (<b>4</b>) were isolated from the crude extract of the plant endophytic fungus <i>Paraconiothynium brasiliense</i> Verkley. The structures of the new compounds were elucidated on the basis of extensive 2D NMR techniques. The absolute configurations of <b>1</b> and <b>2</b> were assigned by <sup>13</sup>C NMR and electronic circular dichroism (ECD) calculations. Furthermore, compounds <b>1 </b>-<b> 4</b> were tested for their cytotoxicity against four human cancer cell lines.</p>","PeriodicalId":15180,"journal":{"name":"Journal of Asian Natural Products Research","volume":" ","pages":"1-10"},"PeriodicalIF":1.3000,"publicationDate":"2025-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Asian Natural Products Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10286020.2025.2477631","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
One new bergamotane-type sesquiterpeniod lactam brasilactam A (1) and one new bergamotane-type sesquiterpeniod spiroketal lactone brasiketalolide A (2), along with two known compounds ampullicin (3) and isoampullicin (4) were isolated from the crude extract of the plant endophytic fungus Paraconiothynium brasiliense Verkley. The structures of the new compounds were elucidated on the basis of extensive 2D NMR techniques. The absolute configurations of 1 and 2 were assigned by 13C NMR and electronic circular dichroism (ECD) calculations. Furthermore, compounds 1 - 4 were tested for their cytotoxicity against four human cancer cell lines.
期刊介绍:
The Journal of Asian Natural Products Research (JANPR) publishes chemical and pharmaceutical studies in the English language in the field of natural product research on Asian ethnic medicine. The journal publishes work from scientists in Asian countries, e.g. China, Japan, Korea and India, including contributions from other countries concerning natural products of Asia. The journal is chemistry-orientated. Major fields covered are: isolation and structural elucidation of natural constituents (including those for non-medical uses), synthesis and transformation (including biosynthesis and biotransformation) of natural products, pharmacognosy, and allied topics. Biological evaluation of crude extracts are acceptable only as supporting data for pure isolates with well-characterized structures.
All published research articles in this journal have undergone rigorous peer review, based on initial editor screening and anonymized refereeing by at least two expert referees.