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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th-cmuir.6653943832-386482015-06-16T07:53:46Z Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers Phothongkam S. Chancharunee S. Saovapakhiran A. Wichai U. Pohmakotr M. Clinical Biochemistry Drug Discovery Pharmaceutical Science Molecular Medicine Molecular Biology Organic Chemistry Biochemistry 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. 2015-06-16T07:53:46Z 2015-06-16T07:53:46Z 2012-12-15 Article 0960894X 2-s2.0-84870236110 10.1016/j.bmcl.2012.10.020 23103096 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84870236110&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38648 Elsevier Limited |
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Clinical Biochemistry Drug Discovery Pharmaceutical Science Molecular Medicine Molecular Biology Organic Chemistry Biochemistry Phothongkam S. Chancharunee S. Saovapakhiran A. Wichai U. Pohmakotr M. Facile synthesis and anticancer activity of C-10 non-acetal deoxoartemisinin dimers |
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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. |
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Article |
author |
Phothongkam S. Chancharunee S. Saovapakhiran A. Wichai U. Pohmakotr M. |
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 |
publisher |
Elsevier Limited |
publishDate |
2015 |
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http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84870236110&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38648 |
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