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Identification and Characterization of Small-Molecule Inducers of Fetal Hemoglobin

Authors
Nam, Tae-gyuLee, JongkookWalker, John R.Brinker, AchimCho, Charles Y.Schultz, Peter G.
Issue Date
May-2011
Publisher
WILEY-BLACKWELL
Keywords
fetal hemoglobin; high-throughput screening; sickle cell disease; STAT3
Citation
CHEMMEDCHEM, v.6, no.5, pp.777 - 780
Indexed
SCIE
SCOPUS
Journal Title
CHEMMEDCHEM
Volume
6
Number
5
Start Page
777
End Page
780
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/38055
DOI
10.1002/cmdc.201000505
ISSN
1860-7179
Abstract
Induction of γ-globin, a component of fetal hemoglobin (HbF, α2γ2), represents one therapeutic strategy to ameliorate the pathological symptoms of sickle cell disease. A high-throughput screen of a large chemical library identified a 2,6-diamino-substituted purine, TN1, which induces HbF more potently than hydroxyurea in KU812 and K562 leukemia cell lines.
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