Structure identification and prophylactic antimalarial efficacy of 2-guanidinoimidazolidinedione derivatives
| Autor: | Gettayacamin Montip, Jian Guan, Charles A. DiTusa, Donald R. Skillman, Wilbur K. Milhous, Quan Zhang, Ai J. Lin, Jean M. Karle |
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| Rok vydání: | 2005 |
| Předmět: |
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Molecular Carbamate Magnetic Resonance Spectroscopy medicine.medical_treatment Clinical Biochemistry Pharmaceutical Science Crystallography X-Ray Guanidines Biochemistry Antimalarials Drug Discovery medicine Animals Organic chemistry Molecule Malaria Falciparum Solubility Molecular Biology Alkyl chemistry.chemical_classification Molecular Structure Organic Chemistry Imidazoles Chemical modification Biological activity Nuclear magnetic resonance spectroscopy Prodrug Macaca mulatta chemistry Molecular Medicine |
| Zdroj: | Bioorganic & Medicinal Chemistry. 13:699-704 |
| ISSN: | 0968-0896 |
| DOI: | 10.1016/j.bmc.2004.10.052 |
| Popis: | The reported synthetic procedure of WR182393, a 2-guanidinoimidazolidinedione derivative with high prophylactic antimalarial activity, was found to be a mixture of three closely related products. Poor solubility of WR182393 in both water and organic solvents and its impractical synthetic method have made the purification and structure identification of the reaction mixture a highly challenging task. The problems were circumvented by prodrug approach involving carbamate formation of the mixture, which enhances the solubility of the mixture in common organic solvents and facilitates the separation and structure determination of the two products. The structures of the two components were determined by X-ray crystallography and NMR of their corresponding carbamates 3a and 4a. Additional alkyl carbamates were prepared according to the same approach and two new carbamates 3b and 4d were found to possess higher intramuscular (im) efficacy than the parent compound WR182393 against Plasmodium cynomolgi in Rhesus monkey. |
| Databáze: | OpenAIRE |
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