Aconicatisulfonines A and B, Analgesic Zwitterionic C20-Diterpenoid Alkaloids with a Rearranged Atisane Skeleton from Aconitum carmichaelii

التفاصيل البيبلوغرافية
العنوان: Aconicatisulfonines A and B, Analgesic Zwitterionic C20-Diterpenoid Alkaloids with a Rearranged Atisane Skeleton from Aconitum carmichaelii
المؤلفون: Jiangong Shi, Shao Shuai, Chengbo Xu, Tiantai Zhang, Huan Xia, Yu-Zhuo Wu, Qing-Lan Guo
المصدر: Organic Letters. 21:6850-6854
بيانات النشر: American Chemical Society (ACS), 2019.
سنة النشر: 2019
مصطلحات موضوعية: biology, 010405 organic chemistry, Stereochemistry, Chemistry, Alkaloid, Organic Chemistry, Analgesic, 010402 general chemistry, biology.organism_classification, 01 natural sciences, Biochemistry, Skeleton (computer programming), Molecular conformation, Terpenoid, 0104 chemical sciences, Aconitum carmichaelii, Acetic acid, chemistry.chemical_compound, Structure–activity relationship, Physical and Theoretical Chemistry
الوصف: Two sulfonated C20-diterpenoid alkaloid iminiums with a novel skeleton, named aconicatisulfonines A (1) and B (2), respectively, were isolated from a water extract of the Aconitum carmichaelii lateral roots. Structures of 1 and 2 were determined by spectroscopic data and quantum calculations as well as X-ray crystallographic analysis. Biosynthetic pathways via semipinacol rearrangements of atisane derivatives are proposed for 1 and 2. Compounds 1 and 2 exhibited remarkable analgesic activities against acetic acid-induced mice writhing.
تدمد: 1523-7052
1523-7060
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e64bac962ce3050fd460e20ca616f69cTest
https://doi.org/10.1021/acs.orglett.9b02479Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........e64bac962ce3050fd460e20ca616f69c
قاعدة البيانات: OpenAIRE