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deferoxamine and Genetic Diseases, X-Chromosome Linked

deferoxamine has been researched along with Genetic Diseases, X-Chromosome Linked in 1 studies

Deferoxamine: Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
desferrioxamine B : An acyclic desferrioxamine that is butanedioic acid in which one of the carboxy groups undergoes formal condensation with the primary amino group of N-(5-aminopentyl)-N-hydroxyacetamide and the second carboxy group undergoes formal condensation with the hydroxyamino group of N(1)-(5-aminopentyl)-N(1)-hydroxy-N(4)-[5-(hydroxyamino)pentyl]butanediamide. It is a siderophore native to Streptomyces pilosus biosynthesised by the DesABCD enzyme cluster as a high affinity Fe(III) chelator.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Heller, T1
Höchstetter, V1
Basler, M1
Borck, V1

Other Studies

1 other study available for deferoxamine and Genetic Diseases, X-Chromosome Linked

ArticleYear
[Vitamin B6-sensitive hereditary sideroblastic anemia].
    Deutsche medizinische Wochenschrift (1946), 2004, Jan-23, Volume: 129, Issue:4

    Topics: Administration, Oral; Adult; Anemia, Sideroblastic; Bone Marrow; Deferoxamine; Diagnosis, Differenti

2004