Michelle van Rensburg
Synthesis and antiproliferative activity of 2-chlorophenyl carboxamide thienopyridines
van Rensburg, Michelle; Leung, Euphemia; Haverkate, Natalie A.; Eurtivong, Chatchakorn; Pilkington, Lisa I.; Reynisson, Jóhannes; Barker, David
Authors
Euphemia Leung
Natalie A. Haverkate
Chatchakorn Eurtivong
Lisa I. Pilkington
Johannes Reynisson j.reynisson@keele.ac.uk
David Barker
Abstract
3-Amino-2-arylcarboxamide-thieno[2,3-b]pyridines are a known class of antiproliferative compounds with activity against the phospholipase C enzyme. To further investigate the structure activity relationships of these derivatives a series of analogues were prepared modifying key functional groups. It was determined that modification of the 3-amino and 2-aryl carboxamide functionalities resulted in complete elimination of activity, whilst modification at C-5 allowed compounds of greater activity to be prepared.
Citation
van Rensburg, M., Leung, E., Haverkate, N. A., Eurtivong, C., Pilkington, L. I., Reynisson, J., & Barker, D. (2017). Synthesis and antiproliferative activity of 2-chlorophenyl carboxamide thienopyridines. Bioorganic and Medicinal Chemistry Letters, 27(2), 135-138. https://doi.org/10.1016/j.bmcl.2016.12.009
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 2, 2016 |
Online Publication Date | Dec 5, 2016 |
Publication Date | 2017-01 |
Deposit Date | Jun 13, 2023 |
Journal | Bioorganic & Medicinal Chemistry Letters |
Print ISSN | 0960-894X |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 27 |
Issue | 2 |
Pages | 135-138 |
DOI | https://doi.org/10.1016/j.bmcl.2016.12.009 |
Keywords | Organic Chemistry; Clinical Biochemistry; Drug Discovery; Pharmaceutical Science; Molecular Biology; Molecular Medicine; Biochemistry |
Additional Information | This article is maintained by: Elsevier; Article Title: Synthesis and antiproliferative activity of 2-chlorophenyl carboxamide thienopyridines; Journal Title: Bioorganic & Medicinal Chemistry Letters; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.bmcl.2016.12.009; Content Type: article; Copyright: © 2016 Elsevier Ltd. All rights reserved. |
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