{"title":"Croton tiglium种子中的Tigliane型二萜类化合物","authors":"Qian-Wen Niu, Lijuan Zhang, Fei-Fei Li, Jianyong Zhu","doi":"10.25135/rnp.344.2205.2455","DOIUrl":null,"url":null,"abstract":": A new tigliane-type diterpenoid ( 1 ) and three known analogues ( 2 − 4 ) were isolated from the seeds of Croton tiglium . Extensive spectroscopic analyses, especially the 2D NMR experiments were used to determine their structures. The absolute configuration of 1 was defined by single-crystal X-ray diffraction data. The cytotoxicity 1 − 4 was evaluated against melanoma cell line A375, and the results showed that compounds 1 , 3 , and 4 exhibited certain cytotoxicities.","PeriodicalId":21053,"journal":{"name":"Records of Natural Products","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2022-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tigliane-Type Diterpenoids from the Seeds of Croton tiglium\",\"authors\":\"Qian-Wen Niu, Lijuan Zhang, Fei-Fei Li, Jianyong Zhu\",\"doi\":\"10.25135/rnp.344.2205.2455\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": A new tigliane-type diterpenoid ( 1 ) and three known analogues ( 2 − 4 ) were isolated from the seeds of Croton tiglium . Extensive spectroscopic analyses, especially the 2D NMR experiments were used to determine their structures. The absolute configuration of 1 was defined by single-crystal X-ray diffraction data. The cytotoxicity 1 − 4 was evaluated against melanoma cell line A375, and the results showed that compounds 1 , 3 , and 4 exhibited certain cytotoxicities.\",\"PeriodicalId\":21053,\"journal\":{\"name\":\"Records of Natural Products\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2022-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Records of Natural Products\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.25135/rnp.344.2205.2455\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Records of Natural Products","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.25135/rnp.344.2205.2455","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Tigliane-Type Diterpenoids from the Seeds of Croton tiglium
: A new tigliane-type diterpenoid ( 1 ) and three known analogues ( 2 − 4 ) were isolated from the seeds of Croton tiglium . Extensive spectroscopic analyses, especially the 2D NMR experiments were used to determine their structures. The absolute configuration of 1 was defined by single-crystal X-ray diffraction data. The cytotoxicity 1 − 4 was evaluated against melanoma cell line A375, and the results showed that compounds 1 , 3 , and 4 exhibited certain cytotoxicities.
期刊介绍:
Records of Natural Products is a journal of natural product chemistry. Reviews, book reviews, research papers and short reports are considered on the substances of plants, microbes and animals.
Discussions on the structure elucidation, synthesis of naturally occurring compounds and biological activity of natural compounds and plant extracts, biosynthesis of natural products and essential oils of aromatic plants as well as chemotaxonomy in the field of plants are welcomed in the journal.
All published research articles in Records of Natural Products have undergone rigorous peer review, based on initial editor screening and anonymized refereeing by expert referees.