Dihydroethanoanthracene Derivatives as In Vitro Malarial Chloroquine Resistance Reversal Agents
Author:
Affiliation:
1. Unité de Parasitologie, Institut de Médecine Tropicale du Service de Santé des Armées
2. Institut Fédératif de la Recherche 48, Marseille, France
3. GERCTOP-UMR CNRS 6009, Faculté de Pharmacie
Abstract
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Link
https://journals.asm.org/doi/pdf/10.1128/AAC.48.7.2753-2756.2004
Reference29 articles.
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2. Alibert, S., C. Santelli-Rouvier, B. Pradines, C. Houdoin, D. Parzy, J. Karolak-Wojciechowska, and J. Barbe. 2002. Synthesis and effects on chloroquine susceptibility in Plasmodium falciparum of a series of new dihydroanthracene derivatives. J. Med. Chem.45:3195-3209.
3. Alibert-Franco, S., C. Santelli-Rouvier, J. Barbe, B. Pradines, C. Houdoin, and D. Parzy. 1999. 9,10-(3′,4′-pyrrolidino)-9,10-dihydroanthracene and structurally related compounds as synergistic antimalarial drugs. Heterocyclic Comm.5:235-240.
4. Barnes, A. J., E. L. Ong, E. M. Dunbar, B. K. Mandal, and E. G. L. Wilkins. 1991. Failure of chloroquine and proguanil prophylaxis in travellers to Kenya. Lancet338:1338-1339.
5. Basco, L. K., P. Ringwald, and J. Le Bras. 1991. Chloroquine potentiating action of antihistaminics in Plasmodium falciparum in vitro. Ann. Trop. Med. Parasitol.85:223-228.
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