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crenolanib

Known as: [1-[2-[5-(3-Methyloxetan-3-ylmethoxy)benzimidazol-1-yl]quinolin-8-yl]piperidin-4-yl]amine, PDGFR Inhibitor CP-868596, PDGFR inhibitor CP-868,596 
An orally bioavailable benzimidazole targeting the platelet-derived growth factor receptor (PDGFR) subtypes alpha and beta and FMS-related tyrosine… 
National Institutes of Health

Papers overview

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2019
2019
Charakteristika der „neuen“ FLT-3-Inhibitoren Crenolanib ist ein starker Typ-1-Inhibitor, der gegen FLT3-ITD und FLT3-D835… 
2018
2018
FLT3, KIT and CSF1R are members of the class III receptor tyrosine kinase family, characterized by an autoinhibitory… 
2017
2017
Tyrosine kinase inhibitors (TKI) have limited impact as single agents in FLT3-ITD+ acute myeloid leukemia (AML), failing to… 
2016
2016
Crenolanib, a type I pan FLT3 inhibitor, had activity in a group of patients with FLT3-positive acute myeloid leukemia (AML… 
2013
2013
The present invention is constitutively active and use of Crenolanib pharmaceutically acceptable salt form in the treatment of… 
2013
2013
A composition comprising a therapeutically effective amount of crenolanib or a pharmaceutically acceptable salt thereof for use… 
2013
2013
Inflammatory breast cancer (IBC) is the most lethal form of locally advanced breast cancer and carries a guarded prognosis. IBC…