Zeitschrift für Naturforschung B · 2012 · 16 citations · 25 references
Organic ChemistryPharmacotherapyHeterocycle ChemistryAntiviral DrugPharmaceutical ChemistryNew Aryl-1,3-thiazole-4-carbohydrazidesMolecular PharmacologyMedicinal ChemistryAntiviral Drug DevelopmentTheir 1,3,4-Oxadiazole-2-Arylthiazolyl Carbohydrazide AnalogsCarboxamide DerivativesDerivativesCompounds 9BHobt/dcc ReagentsHivPharmacologyAntiviral CompoundBiomolecular EngineeringNatural SciencesAntiviral TherapyMedicineSmall MoleculesDrug Discovery
A series of isatin-3-ylidene (6a-i) and arylthiazolyl-1,3,4-oxadiazole-2-thione derivatives 7a-i derived from arylthiazolyl carbohydrazide analogs 4a-i were synthesized. Analogously, coupling of 4f with various amino acid methyl esters in the presence of HOBt/DCC reagents afforded the carboxamide derivatives 9a-d. The newly synthesized compounds were assayed against HIV-1 and HIV-2 in MT-4 cells. All compounds are inactive, except compounds 9b and 9c which showed inhibition of HIV-1 with EC 50 = 2:34 μg mL -1 , and 1.12 μg mL -1 with therapeutic indexes (SI) of 9 and <1, respectively.
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Hiroaki Mitsuya, Kent J. Weinhold, P A Furman et al. · Proceedings of the National Academy of Sciences · 1985 · 1.8K citations · Full text
Ali A. El‐Emam, Omar A. Al‐Deeb, Mohamed A. Al‐Omar et al. · Bioorganic & Medicinal Chemistry · 2004 · 357 citations
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Molecular Biology, Small Substituents, Heterocycle Chemistry +16