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• W2885688891 startingPage "339" @default.
• W2885688891 abstract "Leishmaniasis is an infectious disease caused by various species of protozoan parasite known as Leishmania, which is transmitted to its mammalian host via bite of an infected sandfly. Clinically, Leishmaniasis appears as following four conditions: Cutaneous Leishmaniasis, Mucocutaneous Leishmaniasis, Visceral Leishmaniasis/Kala-azar, Post Kala azar dermal Leishmaniasis. Current therapies include pentavalent antimonials, Amphotericin B, Paromomycin, Miltefosine, Pentamidine, Sitamaquine. Presence of diverse survival pathways in the parasite to carry out various physiological functions has rendered targeting via drugs inefficient and troublesome. Moreover, emerging resistance mechanisms in the well-established key targets are affecting the use of current drug treatment options thus leading to treatment failure. Therefore, development of novel anti-leishmanial compounds with alternative and efficient mechanisms of actions is required to eradicate this disease. This review provides an overview of leishmaniasis along with the main emphasis on novel heterocycles reported for their anti-leishmanial activity in recent years." @default.
• W2885688891 created "2018-08-22" @default.
• W2885688891 creator A5004042220 @default.
• W2885688891 creator A5024604731 @default.
• W2885688891 creator A5082481022 @default.
• W2885688891 date "2018-09-01" @default.
• W2885688891 modified "2023-10-12" @default.
• W2885688891 title "An update on small molecule strategies targeting leishmaniasis" @default.
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• W2885688891 doi "https://doi.org/10.1016/j.ejmech.2018.08.012" @default.
• W2885688891 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30099256" @default.
• W2885688891 hasPublicationYear "2018" @default.
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