نتایج جستجو برای: chelators

تعداد نتایج: 2210  

Journal: :Pharmacological reviews 2005
Danuta S Kalinowski Des R Richardson

The evolution of iron chelators from a range of primordial siderophores and aromatic heterocyclic ligands has lead to the formation of a new generation of potent and efficient iron chelators. For example, various siderophore analogs and synthetic ligands, including ICL670A [4-[3,5-bis-(hydroxyphenyl)-1,2,4-triazol-1-yl]-benzoic acid], 4'-hydroxydesazadesferrithiocin, and Triapine, have been dev...

Journal: :Current Opinion in Chemical Biology 2013

Journal: :PloS one 2015
Pabla Aguirre Natalia P Mena Carlos M Carrasco Yorka Muñoz Patricio Pérez-Henríquez Rodrigo A Morales Bruce K Cassels Carolina Méndez-Gálvez Olimpo García-Beltrán Christian González-Billault Marco T Núñez

Neuronal death in Parkinson's disease (PD) is often preceded by axodendritic tree retraction and loss of neuronal functionality. The presence of non-functional but live neurons opens therapeutic possibilities to recover functionality before clinical symptoms develop. Considering that iron accumulation and oxidative damage are conditions commonly found in PD, we tested the possible neuritogenic ...

Journal: :Hematology. American Society of Hematology. Education Program 2010
Ellis J Neufeld

Over the past four decades, there have been dramatic improvements in survival for patients with thalassemia major due in large measure to improved iron chelators. Two chelators are approved for use in the United States and Canada, parenteral deferoxamine and oral deferasirox. Three are available in much of the rest of the world, where oral deferiprone is also approved (in the United States, def...

2017
José A G Pertusa Trinidad León-Quinto Genoveva Berná Juan R Tejedo Abdelkrim Hmadcha Francisco J Bedoya Franz Martín Bernat Soria

β-cells release hexameric Zn2+-insulin into the extracellular space, but monomeric Zn2+-free insulin appears to be the only biologically active form. The mechanisms implicated in dissociation of the hexamer remain unclear, but they seem to be Zn2+ concentration-dependent. In this study, we investigate the influence of albumin binding to Zn2+ on Zn2+-insulin dissociation into Zn2+-free insulin a...

2006
Shigeki KOBAYASHI Atuhiro MIZUSHIMA Asako SASUGA Makoto WATANABE

Many studies have described the determination of luminescence, radiotherapeutic applications, and development of chelators for lanthanide ions (Ln ) in the past several years. In the application of lanthanide ions for photometry, fluorometry and bioassay, the development of selective chelators and probes for lanthanide ions is important. The electronic configurations of lanthanide ions have 4f ...

Journal: :Al-Azhar Journal of Pediatrics 2022

β-thalassemia is one of the most common hereditary diseases in Egypt. The leading causes renal dysfunction thalassemic patients include chronic anemia, iron overload from repeated blood transfusions, and kidney-induced damage use chelators.

Journal: :Free radical biology & medicine 2008
Brandon J Reeder Robert C Hider Michael T Wilson

Iron chelators such as desferrioxamine have been shown to ameliorate oxidative damage in vivo. The mechanism of this therapeutic action under non-iron-overload conditions is, however, complex, as desferrioxamine has properties that can impact on oxidative damage independent of its capacity to act as an iron chelator. Desferrioxamine can act as a reducing agent to remove cytotoxic ferryl myoglob...

Journal: :Blood 1988
D G Heppner P E Hallaway G J Kontoghiorghes J W Eaton

The appearance of widespread multiple drug resistance in human malaria has intensified the search for new antimalarial compounds. Metal chelators, especially those with high affinity for iron, represent one presently unexploited class of antimalarials. Unfortunately the use of previously identified chelators as antimalarials has been precluded by their toxicity and, in the case of desferrioxami...

Journal: :Journal of neurophysiology 2000
N Chen T H Murphy L A Raymond

Calcium chelators have been widely used in electrophysiological recordings of N-methyl-D-aspartate (NMDA) receptor-mediated currents, as well as in studies of excitotoxicity. Intracellularly applied calcium chelators are known to inhibit, at least in part, such calcium-dependent processes as calmodulin-dependent inactivation, calcineurin-dependent desensitization, and rundown of NMDA receptors....

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