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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…
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National Institutes of Health
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Related topics
Related topics
7 relations
FLT3 protein, human
Mast/Stem Cell Growth Factor Receptor Kit, human
Platelet-Derived Growth Factor Receptor Beta, Human
Receptor Tyrosine Kinase Inhibition
Narrower (1)
MLN-518
Broader (2)
Piperazines
Quinazolines
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Synthesis of Novel Thieno[2,3-d]pyrimidine Derivatives and Evaluation of Their Cytotoxicity and EGFR Inhibitory Activity.
M. Adly
,
E. M. Gedawy
,
A. El-Malah
,
F. El-Telbany
Anti-Cancer Agents in Medicinal Chemistry
2018
Corpus ID: 46799034
BACKGROUND 4-Substitutedaminoquinazoline scaffolds were reported to possess potent cytotoxic and EGFR inhibitory activity such as…
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2017
2017
Dual inhibition of Fes and Flt3 tyrosine kinases potently inhibits Flt3-ITD+ AML cell growth
Mark C. Weir
,
S. Hellwig
,
L. Tan
,
Yao Liu
,
N. Gray
,
T. Smithgall
PLoS ONE
2017
Corpus ID: 34845704
Acute myelogenous leukemia (AML) is often associated with activating mutations in the receptor tyrosine kinase, Flt3, including…
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2016
2016
Feasibility and phase I trial of tandutinib in patients with recurrent glioblastoma.
J. Supko
,
S. Grossman
,
+6 authors
T. Batchelor
Journal of Clinical Oncology
2016
Corpus ID: 31575995
2039 Background: Platelet-derived growth factor signaling is important in gliomagenesis and PDGFR-β is expressed on >90% of…
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2013
2013
Tandutinib (MLN518) reverses multidrug resistance by inhibiting the efflux activity of the multidrug resistance protein 7 (ABCC10)
Wen-jing Deng
,
Chun-ling Dai
,
+5 authors
Zhe-Sheng Chen
Oncology Report
2013
Corpus ID: 15797203
It is well established that ATP-binding cassette (ABC) transporter-mediated multidrug resistance (MDR) is one of the major…
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2013
2013
FLT 3 Inhibitors for the Treatment of Acute Myeloid Leukemia
P. Wiernik
2013
Corpus ID: 37118967
634. 42. Hexner EO, Serdikoff C, Jan M, et al. Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and…
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2012
2012
Preclinical Testing of Tandutinib in a Transgenic Medulloblastoma Mouse Model
S. Ohshima-Hosoyama
,
M. Davare
,
+8 authors
C. Keller
Journal of pediatric hematology/oncology
2012
Corpus ID: 205861897
Overexpression of platelet-derived growth factor receptor alpha (PDGFR-A) has been documented in association with primary tumors…
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2011
2011
Neuromuscular junction toxicity with tandutinib induces a myasthenic-like syndrome
T. Lehky
,
F. Iwamoto
,
T. Kreisl
,
M. Floeter
,
H. Fine
Neurology
2011
Corpus ID: 24729232
Background: Tandutinib (MLN 518, Millennium Pharmaceuticals, Cambridge, MA) is an orally active multitargeted tyrosine kinase…
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Review
2011
Review
2011
Novel and emerging drugs for acute myeloid leukemia: pharmacology and therapeutic activity.
T. Robak
,
A. Szmigielska-Kaplon
,
+4 authors
A. Wierzbowska
Current Medicinal Chemistry
2011
Corpus ID: 23135848
For the last twenty years, significant progress in Molecular and Cellular Biology has resulted in a better characterization and…
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Review
2010
Review
2010
FLT3 inhibitors for the treatment of acute myeloid leukemia.
P. Wiernik
Clinical advances in hematology & oncology : H&O
2010
Corpus ID: 43049364
The fms-like receptor tyrosine kinase-3 (FLT3), which is important for the normal development of hematopoietic stem cells and…
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2008
2008
Tandutinib inhibits FMS receptor signalling, and macrophage and osteoclast formation in vitro
N. Brownlow
,
M. Vaid
,
N. Dibb
Leukemia
2008
Corpus ID: 7078297
Tandutinib inhibits FMS receptor signalling, and macrophage and osteoclast formation in vitro
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