The role of glutathione-S-transferase in anti-cancer drug resistance

DM Townsend, KD Tew - Oncogene, 2003 - nature.com
Abstract Glutathione-S-transferases (GSTs) are a family of Phase II detoxification enzymes
that catalyse the conjugation of glutathione (GSH) to a wide variety of endogenous and …

Antimalarial drug discovery: efficacy models for compound screening

DA Fidock, PJ Rosenthal, SL Croft, R Brun… - Nature reviews Drug …, 2004 - nature.com
Increased efforts in antimalarial drug discovery are urgently needed. The goal must be to
develop safe and affordable new drugs to counter the spread of malaria parasites that are …

Hybrid molecules with a dual mode of action: dream or reality?

B Meunier - Accounts of chemical research, 2008 - ACS Publications
The drug market is still dominated by small molecules, and more than 80% of the clinical
development of drug candidates in the top 20 pharmaceutical firms is still based on small …

Oxidative stress in malaria parasite-infected erythrocytes: host–parasite interactions

K Becker, L Tilley, JL Vennerstrom, D Roberts… - International journal for …, 2004 - Elsevier
Experimenta naturae, like the glucose-6-phosphate dehydrogenase deficiency, indicate that
malaria parasites are highly susceptible to alterations in the redox equilibrium. This offers a …

Next‐generation antimalarial drugs: hybrid molecules as a new strategy in drug design

FW Muregi, A Ishih - Drug development research, 2010 - Wiley Online Library
Malaria is a disease that affects nearly 40% of the global population, and chemotherapy
remains the mainstay of its control strategy. The global malaria situation is increasingly …

New antimalarial drugs

J Wiesner, R Ortmann, H Jomaa… - Angewandte Chemie …, 2003 - Wiley Online Library
Approximately 40% of the world population live in areas with the risk of malaria. Each year,
300–500 million people suffer from acute malaria, and 0.5–2.5 million die from the disease …

Thioredoxin Glutathione Reductase from Schistosoma mansoni: An Essential Parasite Enzyme and a Key Drug Target

AN Kuntz, E Davioud-Charvet, AA Sayed… - PLoS …, 2007 - journals.plos.org
Background Schistosomiasis—infection with helminth parasites in the genus Schistosoma,
including S. mansoni—is a widespread, devastating tropical disease affecting more than …

A review of modifications of quinoline antimalarials: mefloquine and (hydroxy) chloroquine

DJ Kucharski, MK Jaszczak, PJ Boratyński - Molecules, 2022 - mdpi.com
Late-stage modification of drug molecules is a fast method to introduce diversity into the
already biologically active scaffold. A notable number of analogs of mefloquine, chloroquine …

Malaria chemotherapeutics part I: History of antimalarial drug development, currently used therapeutics, and drugs in clinical development

M Schlitzer - ChemMedChem: Chemistry Enabling Drug …, 2007 - Wiley Online Library
Since ancient times, humankind has had to struggle against the persistent onslaught of
pathogenic microorganisms. Nowadays, malaria is still the most important infectious disease …

Methylene blue as an antimalarial agent

RH Schirmer, B Coulibaly, A Stich, M Scheiwein… - Redox …, 2003 - Taylor & Francis
Methylene blue has intrinsic antimalarial activity and it can act as a chloroquine sensitizer. In
addition, methylene blue must be considered for preventing methemoglobinemia, a serious …