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tandutinib

Known as: 1-Piperazinecarboxamide, 4-(6-Methoxy-7-(3-(1-piperidinyl)propoxy)-4-quinazolinyl)-N-(4-(1-methylethoxy)phenyl)-, 4-(6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl)piperazine-1-carboxylic acid (4-isopropoxyphenyl)amide 
A piperazinyl quinazoline receptor tyrosine kinase inhibitor with antineoplastic activity. Tandutinib inhibits the autophosphorylation of FLT3 (FMS… 
National Institutes of Health

Papers overview

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2018
2018
BACKGROUND 4-Substitutedaminoquinazoline scaffolds were reported to possess potent cytotoxic and EGFR inhibitory activity such as… 
2017
2017
Acute myelogenous leukemia (AML) is often associated with activating mutations in the receptor tyrosine kinase, Flt3, including… 
2016
2016
2039 Background: Platelet-derived growth factor signaling is important in gliomagenesis and PDGFR-β is expressed on >90% of… 
2013
2013
It is well established that ATP-binding cassette (ABC) transporter-mediated multidrug resistance (MDR) is one of the major… 
2013
2013
634. 42. Hexner EO, Serdikoff C, Jan M, et al. Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and… 
2012
2012
Overexpression of platelet-derived growth factor receptor alpha (PDGFR-A) has been documented in association with primary tumors… 
2011
2011
Background: Tandutinib (MLN 518, Millennium Pharmaceuticals, Cambridge, MA) is an orally active multitargeted tyrosine kinase… 
Review
2011
Review
2011
For the last twenty years, significant progress in Molecular and Cellular Biology has resulted in a better characterization and… 
Review
2010
Review
2010
The fms-like receptor tyrosine kinase-3 (FLT3), which is important for the normal development of hematopoietic stem cells and… 
2008
2008
Tandutinib inhibits FMS receptor signalling, and macrophage and osteoclast formation in vitro