Two new yohimbine-type monoterpene indole alkaloids, rauvines A and B, and six known derivatives were obtained from the leaves of R. vomitoria. The structures of rauvines A and B were determined by extensive spectroscopic analyses, C-NMR, and ECD calculations. This is the first time to determine the absolute configurations of yohimbine-type N-oxides by quantum chemistry calculations ( C-NMR and ECD calculations). All the isolates were tested for their cytotoxicity against five human cancer cell lines. Rauvine B showed moderate cytotoxicity on human MCF-7 breast, SWS80 colon, and A549 lung cancer cell lines with IC values of 25.5, 22.6, and 26.0 μM, respectively.
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http://dx.doi.org/10.1002/cbdv.202000647 | DOI Listing |
Phytochemistry
December 2024
College of Marine Sciences and Biotechnology, Guangxi Key Laboratory of Polysaccharide Materials and Modification, Guangxi Minzu University, Nanning, 530008, China. Electronic address:
Nine previously undescribed azulenoid-type sesquiterpenoids, including four common (1-4), four 5/6-cleaved (5-8), and one rearranged (9), were isolated from the edible-medicinal fungi Irpex lacteus. The structures of the compounds were established by combining spectroscopic methods, including integrated NMR, MS, and UV, as well as quantum C NMR and ECD calculations. All compounds exhibited a meaningful reduction in triglycerides activity.
View Article and Find Full Text PDFPhytochemistry
December 2024
Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Ministry of Education, Gannan Medical University, Ganzhou, Jiangxi, 341000, China; Jiangxi Provincal Key Laboratory of Tissue Engineering, 2024SSY06291, Gannan Medical University, Ganzhou, Jiangxi, 341000, China; School of Pharmacy, Nanchang Medical College, Nanchang, Jiangxi, 330052, China. Electronic address:
Thirteen abietane-type diterpenoids, including seven previously undescribed compounds and six known analogs, were isolated from the root and aerial parts of Phlegmariurus carinatus. Their structures were elucidated by comprehensive spectroscopic data analysis (UV, IR, NMR, and HRESIMS) and quantum chemical calculations (calculated ECD or C NMR). Notably, these compounds exhibited high structural diversity.
View Article and Find Full Text PDFNat Prod Res
November 2024
Center of Excellence for Innovation in Chemistry (PERCH-CIC), Department of Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, Thailand.
Fitoterapia
January 2025
Guangdong Key Laboratory for Research and Development of Natural Drugs, The First Dongguan Affiliated Hospital, School of Pharmacy, Guangdong Medical University, Dongguan 523808, China; College of Pharmacy, Jinan University, #855Xingye Avenue, Guangzhou 510632, China; Dongguan Key Laboratory for Marine Innovative Drugs and Bioproducts, Guangdong Medical University, Dongguan 523808, China. Electronic address:
Ten new limonoids, named xylomolones E-N (1-10), and two new protolimonoids, named xylomolones O (11) and P (12), were isolated from seeds of the Thai mangrove Xylocarpus moluccensis, together with the known compound, hispidone acetonide (13). The structures of these compounds were established by extensive NMR spectroscopic data, single-crystal X-ray diffraction analysis, and comparison of experimental ECD spectra. The absolute configurations of xylomolones E (1) and L (8) were unambiguously determined by single-crystal X-ray diffraction analyses, conducted with Cu Kα radiation.
View Article and Find Full Text PDFPhytochemistry
February 2025
State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization and The Key Laboratory of Plants Resources and Chemistry of Arid Zone, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, China; University of Chinese Academy of Sciences, Beijing, 100049, China; College of Pharmacy, Xinjiang Medical University, Urumqi 830011, China. Electronic address:
Eleven undescribed sesquiterpenes, vachanins A-K covering types of germacrane, eudesmane, guaiacane, and cadinane, along with fifteen known analogs were isolated from the aerial parts of Artemisia vachanica Krasch. ex Poljakov. Their structures were established on the basis of HRMS and NMR data, and their absolute configurations were successfully determined by single-crystal X-ray diffraction analysis, C-NMR calculations and DP4+ probability analysis, and ECD data in corporation with quantum chemical calculations.
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