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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18371
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dc.contributor.authorKumar, Gautam-
dc.date.accessioned2025-03-15T05:16:24Z-
dc.date.available2025-03-15T05:16:24Z-
dc.date.issued2018-04-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0223523418301016-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18371-
dc.description.abstractA series of pyrazole-pyrazoline substituted with benzenesulfonamide were synthesized and evaluated for their antimalarial activity in vitro and in vivo. The compounds were active against both chloroquine (CQ) sensitive (3D7) and CQ resistant (RKL-9) strains of Plasmodium falciparum. Seven compounds (7e, 7i, 7j, 7l, 7m, 7o and 7p) exhibiting EC50 less than 2 μM. A mechanistic study of compound 7o revealed that these compound act through the inhibition of β-hematin. The study indicated that these compounds can serve as lead compounds for further development of potent antimalarial drugs.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPharmacyen_US
dc.subjectPlasmodium falciparumen_US
dc.subjectAntimalarialen_US
dc.subjectHeme bindingen_US
dc.subjectPyrazolineen_US
dc.titlePyrazole-pyrazoline as promising novel antimalarial agents: a mechanistic studyen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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