1. Academic Validation
  2. Structurally Diverse Alkaloids from the Seeds of Peganum harmala

Structurally Diverse Alkaloids from the Seeds of Peganum harmala

  • J Nat Prod. 2017 Feb 24;80(2):551-559. doi: 10.1021/acs.jnatprod.6b01146.
Kai-Bo Wang 1 Da-Hong Li Yu Bao Fei Cao 2 Wen-Jing Wang Clement Lin 1 Wen Bin Jiao Bai Yue-Hu Pei Yong-Kui Jing Danzhou Yang 1 Zhan-Lin Li Hui-Ming Hua
Affiliations

Affiliations

  • 1 Department of Medicinal Chemistry and Molecular Pharmacology, College of Pharmacy, Purdue University , West Lafayette, Indiana 47907, United States.
  • 2 Key Laboratory of Pharmaceutical Quality Control of Hebei Province, College of Pharmaceutical Sciences, Hebei University , Baoding 071002, People's Republic of China.
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.

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