| Literature DB >> 28128938 |
Kai-Bo Wang1, Da-Hong Li, Yu Bao, Fei Cao2, Wen-Jing Wang, Clement Lin1, Wen Bin, Jiao Bai, Yue-Hu Pei, Yong-Kui Jing, Danzhou Yang1, Zhan-Lin Li, Hui-Ming Hua.
Abstract
Investigation of the alkaloids from Peganum harmala seeds yielded two pairs of unique racemic pyrroloindole alkaloids, (±)-peganines A-B (1-2); two rare thiazole derivatives, peganumals A-B (3-4); six new β-carboline alkaloids, pegaharmines F-K (5-10); and 12 known analogues. Their structures, including stereochemistry, were elucidated through spectroscopic analyses, quantum chemistry calculations, and single-crystal X-ray diffraction. Notably, the incorporation of pyrrole and indole moieties in peganines A-B, thiazole fragments in peganumals A-B, and a C-1 α,β-unsaturated ester motif in pegaharmine F (5) are all rare, and their presence in the genus Peganum were demonstrated for the first time. All isolates were tested for antiproliferative activities against the HL-60, PC-3, and SGC-7901 cancer cell lines, and compounds 9, 11, 12, and 13 exhibited moderate cytotoxicity against HL-60 cancer cell lines with IC50 values in the range of 4.36-9.25 μM.Entities:
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Year: 2017 PMID: 28128938 PMCID: PMC5518681 DOI: 10.1021/acs.jnatprod.6b01146
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050