"One-Pot" Synthesis and Antimalarial Activity of Formamidine Derivatives of 4-Anilinoquinoline.
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- DELARUE Sandrine
- UMR CNRS 8525, Institut de Biologie et Institut Pasteur de Lille, Faculté de Pharmacie, Université de Lille II
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- GIRAULT Sophie
- UMR CNRS 8525, Institut de Biologie et Institut Pasteur de Lille, Faculté de Pharmacie, Université de Lille II
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- DALI ALI Fouad
- Laboratoire de Biologie Parasitaire, IFR CNRS 63, Muséum National d’Histoire Naturelle
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- MAES Louis
- TIBOTEC, L11 Général de Wittelaan
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- GRELLIER Philippe
- Laboratoire de Biologie Parasitaire, IFR CNRS 63, Muséum National d’Histoire Naturelle
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- SERGHERAERT Christian
- UMR CNRS 8525, Institut de Biologie et Institut Pasteur de Lille, Faculté de Pharmacie, Université de Lille II
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Abstract
Amodiaquine (AQ) is an antimalarial which is effective against chloroquino-resistant strains of Plasmodium falciparum but whose clinical use is severely restricted because of associated hepatotoxicity and agranulocytosis. “One-pot” synthesis of formamidines likely to be transformed into AQ derivatives is reported. Compared with AQ, the new compounds were devoid of in vitro cytotoxicity upon human embryonic lung cells and mouse peritoneal macrophages. One showed a potent in vivo activity in mice infected with P. berghei. Transformation of this compound by reductive amination led to a new type of AQ derivatives that displayed an in vitro activity similar to that of AQ but did not lead to toxic quinone-imines.
Journal
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- Chemical and Pharmaceutical Bulletin
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Chemical and Pharmaceutical Bulletin 49 (8), 933-937, 2001
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390001204162068736
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- NII Article ID
- 110003616023
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- NII Book ID
- AA00602100
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- COI
- 1:CAS:528:DC%2BD3MXlvVCnu78%3D
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- ISSN
- 13475223
- 00092363
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- NDL BIB ID
- 5850704
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- PubMed
- 11515580
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed