2011
DOI: 10.1016/j.bmc.2010.12.028
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New imidazolidinedione derivatives as antimalarial agents

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Cited by 16 publications
(28 citation statements)
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“…Imidazolidinedione compounds are oxygen and N‐heterocyclic nonaromatic compounds with ketone groups that have been identified in the pyrolysis of glycine or human hair . It has been suggested that these N‐heterocyclic compounds are formed during amino acid pyrolysis . Imidazolidinedione derivatives are considered to be valuable products thanks to their pharmacological, antibacterial, antifungal, antiprotozoal, antimalarial, or anthelmintic properties .…”
Section: Resultsmentioning
confidence: 99%
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“…Imidazolidinedione compounds are oxygen and N‐heterocyclic nonaromatic compounds with ketone groups that have been identified in the pyrolysis of glycine or human hair . It has been suggested that these N‐heterocyclic compounds are formed during amino acid pyrolysis . Imidazolidinedione derivatives are considered to be valuable products thanks to their pharmacological, antibacterial, antifungal, antiprotozoal, antimalarial, or anthelmintic properties .…”
Section: Resultsmentioning
confidence: 99%
“…[78] It has been suggestedt hat these N-heterocyclic compounds are formed during amino acid pyrolysis. [79] Imidazolidinedione derivatives are considered to be valuable products thankst ot heir pharmacological, antibacterial, antifungal, antiprotozoal, antimalarial, or anthelmintic properties. [79] They could also be formed from melanoidin compounds,w hich are generatedi nt he Maillardr eactionf rom reducing sugars and proteinso ra mino acids.…”
Section: Imidazolidinedione Compoundsmentioning
confidence: 99%
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“…Data are reported for primaquine, 40 ato-vaquone, 41,42 proguanil, 43 and its active metabolite cycloguanil. 44 …”
Section: Methodsmentioning
confidence: 99%
“…CHP) rendszer segítségével a korábban ismert 161 dijódizocianid intermedieren keresztül a 162 karbodiimideket állították elő (25. ábra) 137. A reakció során az izocianidot a katalitikus mennyiségben alkalmazott elemi jód oxidálja, míg a peroxid reagens (CHP) az eliminálódó hidrogén-jodid oxidálásával és elvonásával egyrészt a katalitikus 20-25 °C) rendszerint néhány óra alatt végbemegy [151][152][153][154][155]. A ciánamid izolálását követően erélyes reakciókörülmények (>100 °C) mellett egy újabb amin molekula nukleofil addíciója szolgáltatja a 200 guanidin terméket [151][152][153][154][155].…”
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