Drugs in development for toxoplasmosis: advances, challenges, and current status

PH Alday, JS Doggett - Drug design, development and therapy, 2017 - Taylor & Francis
Toxoplasma gondii causes fatal and debilitating brain and eye diseases. Medicines that are
currently used to treat toxoplasmosis commonly have toxic side effects and require …

Quinolines and structurally related heterocycles as antimalarials

K Kaur, M Jain, RP Reddy, R Jain - European journal of medicinal …, 2010 - Elsevier
The quinoline scaffold is prevalent in a variety of pharmacologically active synthetic and
natural compounds. The discovery of chloroquine, the most famous drug containing this …

The methods of synthesis, modification, and biological activity of 4-quinolones

AA Boteva, OP Krasnykh - Chemistry of heterocyclic compounds, 2009 - Springer
THE METHODS OF SYNTHESIS, MODIFICATION, AND BIOLOGICAL ACTIVITY OF 4-QUINOLONES
(REVIEW) Page 1 Chemistry of Heterocyclic Compounds, Vol. 45, No. 7, 2009 THE …

Bicyclic conformationally restricted diamines

OO Grygorenko, DS Radchenko… - Chemical …, 2011 - ACS Publications
The term “conformational restriction” can be found very often in contemporary chemical
literature. Despite the lack of strict definitions, this term is usually intuitively understood and …

Antibiotics in malaria therapy: which antibiotics except tetracyclines and macrolides may be used against malaria?

T Gaillard, M Madamet, FF Tsombeng, J Dormoi… - Malaria journal, 2016 - Springer
Malaria, a parasite vector-borne disease, is one of the most significant health threats in
tropical regions, despite the availability of individual chemoprophylaxis. Malaria …

Design, synthesis and activity against Toxoplasma gondii, Plasmodium spp., and Mycobacterium tuberculosis of new 6-fluoroquinolones

G Anquetin, J Greiner, N Mahmoudi… - European journal of …, 2006 - Elsevier
This paper reports on the rational design of a series of new 6-fluoroquinolones by QSAR
analysis against Toxoplasma (T.) gondii, their synthesis, their biological evaluation against …

Synthesis and evaluation of novel 1, 3, 4-thiadiazole--fluoroquinolone hybrids as antibacterial, antituberculosis, and anticancer agents

A Demirci, KG KARAYEL, E Tatar… - Turkish Journal of …, 2018 - journals.tubitak.gov.tr
Abstract A series of 5-substituted-1, 3, 4-thiadiazole-based fluoroquinolone derivatives were
designed as potential antibacterial and anticancer agents using a molecular hybridization …

The anticoccidial activity of the fluoroquinolone lomefloxacin against experimental Eimeria tenella infection in broiler chickens

KA El-Shazly, AA El-Latif, W Abdo, A El-Morsey… - Parasitology …, 2020 - Springer
Coccidiosis is a crucial parasitic disease of the poultry industry. As a result of the enormous
global economic losses and the increased resistance to the conventional anticoccidial …

Evaluation of the in vitro activity of commercially available moxifloxacin and voriconazole eye-drops against clinical strains of Acanthamoeba

CM Martín-Navarro, A López-Arencibia… - Graefe's Archive for …, 2013 - Springer
Purpose Acanthamoeba is an opportunistic pathogen which is the causal agent of a sight-
threatening ulceration of the cornea known as “Acanthamoeba keratitis”(AK) and, more …

Synthesis and antimalarial activity of pyrazolo and pyrimido benzothiazine dioxide derivatives

A Barazarte, G Lobo, N Gamboa, JR Rodrigues… - European journal of …, 2009 - Elsevier
A series of phenylsubstituted pyrazolo and pyrimido benzothiazine dioxide derivatives were
synthesized and investigated for their abilities to inhibit β-hematin formation, hemoglobin …