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Molecules 2010, 15(4), 2398-2404; https://doi.org/10.3390/molecules15042398

Pellitorine, a Potential Anti-Cancer Lead Compound against HL60 and MCT-7 Cell Lines and Microbial Transformation of Piperine from Piper Nigrum

1
Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia
2
Department of Crop Science, Faculty of Agriculture & Food Sciences, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia
*
Author to whom correspondence should be addressed.
Received: 12 January 2010 / Revised: 9 March 2010 / Accepted: 18 March 2010 / Published: 5 April 2010
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Abstract

Pellitorine (1), which was isolated from the roots of Piper nigrum, showed strong cytotoxic activities against HL60 and MCT-7 cell lines. Microbial transformation of piperine (2) gave a new compound 5-[3,4-(methylenedioxy)phenyl]-pent-2-ene piperidine (3). Two other alkaloids were also found from Piper nigrum. They are (E)-1-[3’,4’-(methylenedioxy)cinnamoyl]piperidine (4) and 2,4-tetradecadienoic acid isobutyl amide (5). These compounds were isolated using chromatographic methods and their structures were elucidated using MS, IR and NMR techniques.
Keywords: Piper nigrum; pellitorine; alkaloids; cytotoxicity; microbial transformation; aspergillus niger Piper nigrum; pellitorine; alkaloids; cytotoxicity; microbial transformation; aspergillus niger
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).
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Ee, G.C.L.; Lim, C.M.; Rahmani, M.; Shaari, K.; Bong, C.F.J. Pellitorine, a Potential Anti-Cancer Lead Compound against HL60 and MCT-7 Cell Lines and Microbial Transformation of Piperine from Piper Nigrum. Molecules 2010, 15, 2398-2404.

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