Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.

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 Pi...

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Main Authors: Ee , Gwendoline Cheng Lian, Lim, Chyi Meei, Rahmani, Mawardi, Shaari, Khozirah, Bong, Choon Fah Joseph
Format: Article
Language:English
English
Published: MDPI 2010
Online Access:http://psasir.upm.edu.my/id/eprint/16064/1/Pellitorine.pdf
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author Ee , Gwendoline Cheng Lian
Lim, Chyi Meei
Rahmani, Mawardi
Shaari, Khozirah
Bong, Choon Fah Joseph
author_facet Ee , Gwendoline Cheng Lian
Lim, Chyi Meei
Rahmani, Mawardi
Shaari, Khozirah
Bong, Choon Fah Joseph
author_sort Ee , Gwendoline Cheng Lian
collection UPM
description 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.
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spelling upm.eprints-160642015-09-10T06:54:16Z http://psasir.upm.edu.my/id/eprint/16064/ Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum. Ee , Gwendoline Cheng Lian Lim, Chyi Meei Rahmani, Mawardi Shaari, Khozirah Bong, Choon Fah Joseph 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. MDPI 2010 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/16064/1/Pellitorine.pdf Ee , Gwendoline Cheng Lian and Lim, Chyi Meei and Rahmani, Mawardi and Shaari, Khozirah and Bong, Choon Fah Joseph (2010) Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum. Molecules, 15 (4). pp. 2398-2404. ISSN 1420-3049 10.3390/molecules15042398 English
spellingShingle Ee , Gwendoline Cheng Lian
Lim, Chyi Meei
Rahmani, Mawardi
Shaari, Khozirah
Bong, Choon Fah Joseph
Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.
title Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.
title_full Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.
title_fullStr Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.
title_full_unstemmed Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.
title_short Pellitorine, a potential anti-cancer lead compound against HL60 and MCT-7 cell lines and microbial transformation of piperine from Piper nigrum.
title_sort pellitorine a potential anti cancer lead compound against hl60 and mct 7 cell lines and microbial transformation of piperine from piper nigrum
url http://psasir.upm.edu.my/id/eprint/16064/1/Pellitorine.pdf
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