[HTML][HTML] QSAR and molecular docking studies of 1, 3-dioxoisoindoline-4-aminoquinolines as potent antiplasmodium hybrid compounds

AW Mahmud, GA Shallangwa, A Uzairu - Heliyon, 2020 - cell.com
Quantitative structure–activity relationships (QSAR) provides a model that link biological
activities of compounds to thier chemical stuctures and molecular docking study reveals the …

[HTML][HTML] Toxoplasma gondii: the effect of fluconazole combined with sulfadiazine and pyrimethamine against acute toxoplasmosis in murine model

ÉS Martins-Duarte, W de Souza, RC Vommaro - Experimental parasitology, 2013 - Elsevier
Toxoplasma gondii is an important opportunistic pathogen for immunocompromised patients
and responsible for toxoplasmic encephalitis, which is often lethal. Treatment for this …

In search of suitable protein targets for anti-malarial and anti-dengue drug discovery

PTV Nguyen, GLT Nguyen, OT Đinh, CQ Duong… - Journal of Molecular …, 2022 - Elsevier
Selecting suitable targets is the critical first step in drug discovery. However, for malaria and
dengue this is quite a challenging step due to a large number of available structures for …

Photoaffinity probe‐based antimalarial target identification of artemisinin in the intraerythrocytic developmental cycle of Plasmodium falciparum

P Gao, J Wang, C Qiu, H Zhang, C Wang, Y Zhang… - iMeta, 2024 - Wiley Online Library
Malaria continues to pose a serious global health threat, and artemisinin remains the core
drug for global malaria control. However, the situation of malaria resistance has become …

A novel compound purified from Alstonia boonei inhibits Plasmodium falciparum lactate dehydrogenase and plasmepsin II

JO Olanlokun, AF Olotu, OM David… - Journal of …, 2019 - Taylor & Francis
Malarial infection is a disease that has defied many therapeutic and chemopreventive
interventions due to persistent resistance to currently available drugs. This is driven by the …

[HTML][HTML] Analogues of Oxamate, Pyruvate, and Lactate as Potential Inhibitors of Plasmodium knowlesi Lactate Dehydrogenase Identified Using Virtual Screening and …

FA Ahmad Fuad, N Ogu Salim - Processes, 2022 - mdpi.com
Malaria management remains a challenge, due to the resistance of malaria parasites to
current antimalarial agents. This resistance consequently delays the global elimination of …

High-efficiency production of Plasmodium falciparum lactate dehydrogenase from bacteria and its functional characterization

YJ Kim, G Ahn, JY Ahn, JW Choi - Process Biochemistry, 2024 - Elsevier
Plasmodium falciparum is the pathogen responsible for 90% of all malaria cases and is
associated with severe complications and the highest fatality rate. Plasmodium falciparum …

A structure guided drug-discovery approach towards identification of Plasmodium inhibitors

B Aneja, B Kumar, MA Jairajpuri, M Abid - RSC advances, 2016 - pubs.rsc.org
Rapidly increasing resistance to the currently available antimalarial drugs has drawn
attention globally for the search for more potent novel drugs with a high therapeutic index …

Cloning, overexpression, purification and characterization of Plasmodium knowlesi lactate dehydrogenase

V Singh, DC Kaushal, S Rathaur, N Kumar… - Protein expression and …, 2012 - Elsevier
Plasmodial lactate dehydrogenase, key enzyme of anaerobic glycolysis, has been shown to
be a potential immunodiagnostic marker as well as a novel target for chemotherapy. We …

[HTML][HTML] Implementation and continued validation of the malaria Plasmodium falciparum lactate dehydrogenase-based colorimetric assay for use in antiplasmodial …

PVT Fokou, BMT Tali, D Dize, CDJ Mbouna… - Analytical …, 2022 - Elsevier
Antimalarial drug discovery has been facilitated by the development of various in vitro drug
susceptibility testing methods suitable for medium-throughput or high-throughput …