Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers

In this research, N-(2-aminoethyl)glycine-linked C-10 non-acetal deoxoartemisinin dimers were synthesized by using solution phase peptide synthesis approach. In addition, chemical modification of the C-10 non-acetal deoxoartemisinin monomers and dimers by adding a lysine unit to the N-terminus has b...

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Main Authors: Phothongkam S., Chancharunee S., Saovapakhiran A., Wichai U., Pohmakotr M.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84867684733&partnerID=40&md5=39febe766c46a733b4fa0592bfd96673
http://cmuir.cmu.ac.th/handle/6653943832/6915
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-69152014-08-30T03:51:23Z Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers Phothongkam S. Chancharunee S. Saovapakhiran A. Wichai U. Pohmakotr M. In this research, N-(2-aminoethyl)glycine-linked C-10 non-acetal deoxoartemisinin dimers were synthesized by using solution phase peptide synthesis approach. In addition, chemical modification of the C-10 non-acetal deoxoartemisinin monomers and dimers by adding a lysine unit to the N-terminus has been performed. The biological activities of all synthesized compounds were evaluated against the colon cancer cell line (Caco-2). The non-acetal deoxoartemisinin monomers 12a, 15a-c and dimers 13a, 16a-c were active against Caco-2 cells and more potent than dihydroartemisinin. © 2012 Elsevier Ltd. All rights reserved. 2014-08-30T03:51:23Z 2014-08-30T03:51:23Z 2012 Article in Press 0960894X 10.1016/j.bmcl.2012.10.020 BMCLE http://www.scopus.com/inward/record.url?eid=2-s2.0-84867684733&partnerID=40&md5=39febe766c46a733b4fa0592bfd96673 http://cmuir.cmu.ac.th/handle/6653943832/6915 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description In this research, N-(2-aminoethyl)glycine-linked C-10 non-acetal deoxoartemisinin dimers were synthesized by using solution phase peptide synthesis approach. In addition, chemical modification of the C-10 non-acetal deoxoartemisinin monomers and dimers by adding a lysine unit to the N-terminus has been performed. The biological activities of all synthesized compounds were evaluated against the colon cancer cell line (Caco-2). The non-acetal deoxoartemisinin monomers 12a, 15a-c and dimers 13a, 16a-c were active against Caco-2 cells and more potent than dihydroartemisinin. © 2012 Elsevier Ltd. All rights reserved.
format Article
author Phothongkam S.
Chancharunee S.
Saovapakhiran A.
Wichai U.
Pohmakotr M.
spellingShingle Phothongkam S.
Chancharunee S.
Saovapakhiran A.
Wichai U.
Pohmakotr M.
Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers
author_facet Phothongkam S.
Chancharunee S.
Saovapakhiran A.
Wichai U.
Pohmakotr M.
author_sort Phothongkam S.
title Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers
title_short Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers
title_full Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers
title_fullStr Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers
title_full_unstemmed Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers
title_sort facile synthesis and anticancer activity of c-10 non-acetal deoxoartemisinin dimers
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84867684733&partnerID=40&md5=39febe766c46a733b4fa0592bfd96673
http://cmuir.cmu.ac.th/handle/6653943832/6915
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