Journal of Enzyme Inhibition and Medicinal Chemistry · 2013 · 33 citations · 33 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoverySynthetic Medicinal ChemistryAntiparasitic AgentsStructure-activity Relationship AnalysisAntileishmanial TreatmentAntimalarial AgentsAntimalarial Drug DevelopmentNovel Antiparasitic Compound ClassesTreatment Of Leishmaniasis
A series of 29 previously reported N(4)-substituted 5-nitroisatin-3-thiosemicarbazones 2-30 has been screened for leishmanicidal potential. Compounds 2-4, 7, 8, 10-13, 15-19, 21, 23, 24, 26, 28 and 30 exhibited good to excellent antileishmanial activities with IC50 values ranging from 0.44 ± 0.02 to 32.38 ± 0.66 µg/mL. Of these, 5, 7, 19 and 28 proved to be the most active antileishmanial agents, displaying activities with IC50 values 1.78 ± 0.35, 0.44 ± 0.02, 1.91 ± 0.04 and 4.28 ± 0.75 µg/mL, respectively, which were even better than the standard drug, pentamidine (IC50 = 5.09 ± 0.04 µg/mL). This study presents the first example of exhibition of leishmanicidal potential by isatin-thiosemicarbazones and as such furnishes a solid basis for further research on these compounds to develop more potent antileishmanial agents.
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Xiaohui Du, Chun Guo, Elizabeth Hansell et al. · Journal of Medicinal Chemistry · 2002 · 383 citations · Full text
Miltefosine for New World Cutaneous Leishmaniasis
Jaime Soto, Byron Arana, Julia Toledo et al. · Clinical Infectious Diseases · 2004 · 381 citations
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Biological activities of isatin and its derivatives.
Surendra N. Pandeya, Sivakumar Smitha, Mayank Jyoti et al. · PubMed · 2005 · 345 citations · Full text