A non-cytotoxic N-dehydroabietylamine derivative with potent antimalarial activity

Sadashiva, M. P. and Gowda, R. and Wu, X. and Inamdar, G. S. and Kuzu, O. F. and Rangappa, K. S. and Robertson, G. P. and Gowda, D. C. (2015) A non-cytotoxic N-dehydroabietylamine derivative with potent antimalarial activity. EXPERIMENTAL PARASITOLOGY, 155. pp. 68-73. ISSN 1090-2449

[img] Text (Full Text)
nihms691160.pdf - Published Version
Restricted to Registered users only

Download (836kB) | Request a copy
Official URL: https://doi.org/10.1016/j.exppara.2015.05.002

Abstract

Malaria caused by the Plasmodium parasites continues to be an enormous global health problem owing to wide spread drug resistance of parasites to many of the available antimalarial drugs. Therefore, development of new classes of antimalarial agents is essential to effectively treat malaria. In this study, the efficacy of naturally occurring diterpenoids, dehydroabietylamine and abietic acid, and their synthetic derivatives was assessed for antimalarial activity. Dehydroabietylamine and its N-trifluoroacetyl, N-tribromoacetyl, N-benzoyl, and N-benzyl derivatives showed excellent activity against P. falciparum parasites with IC50 values of 0.36 to 2.6 mu M. Interestingly, N-dehydroabietylbenzamide showed potent antimalarial activity (IC50 0.36), and negligible cytotoxicity (IC50 >100 mu M) to mammalian cells; thus, this compound can be an important antimalarial drug. In contrast, abietic acid was only marginally effective, exhibiting an IC50 value of similar to 82 mu M. Several carboxylic group-derivatives of abietic acid were moderately active with IC50 values of similar to 8.2 to similar to 13.3 mu M. These results suggest that a detailed understanding of the structure-activity relationship of abietane diterpenoids might provide strategies to exploit this class of compounds for malaria treatment. (C) 2015 Elsevier Inc. All rights reserved.

Item Type: Article
Uncontrolled Keywords: Abietane diterpenoids; Dehydroabietylamine derivatives; Abietic acid derivatives; Antimalarial activity
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: Shrirekha N
Date Deposited: 03 Jun 2019 05:35
Last Modified: 03 Jun 2019 05:35
URI: http://eprints.uni-mysore.ac.in/id/eprint/2077

Actions (login required)

View Item View Item