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NVP-LAF237

Known as: NVP-LAF-237 
 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

vildagliptin

Papers overview

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2018
2018
Targeting BCR-ABL-Independent TKI Resistance in Chronic Myeloid Leukemia by mTOR and Autophagy Inhibition
Background Imatinib and second-generation tyrosine kinase inhibitors (TKIs) nilotinib and dasatinib have statistically… Expand
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2015
2015
The small molecule tyrosine kinase inhibitor NVP-BHG712 antagonizes ABCC10-mediated paclitaxel resistance: a preclinical and pharmacokinetic study
Paclitaxel exhibits clinical activity against a wide variety of solid tumors. However, resistance to paclitaxel significantly… Expand
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Highly Cited
2010
Highly Cited
2010
89Zr-bevacizumab PET of early antiangiogenic tumor response to treatment with HSP90 inhibitor NVP-AUY922.
UNLABELLED Angiogenesis is a critical step in tumor development, in which vascular endothelial growth factor (VEGF) is a key… Expand
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Highly Cited
2010
Highly Cited
2010
Novel HSP90 inhibitors, NVP-AUY922 and NVP-BEP800, radiosensitise tumour cells through cell-cycle impairment, increased DNA damage and repair protraction
Background:Heat-shock protein 90 (Hsp90) has a crucial role in both the stabilisation and regulation of various proteins… Expand
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2010
2010
89 Zr-Bevacizumab PET of Early Antiangiogenic Tumor Response to Treatment with HSP 90 Inhibitor NVP-AUY 922
1Department of Medical Oncology, University of Groningen, Groningen, The Netherlands; 2Department of Pathology, University of… Expand
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2009
2009
The metabolic modulators, Etomoxir and NVP-LAB121, fail to reverse pressure overload induced heart failure in vivo
Shifting substrate oxidation in heart muscle from fatty acids to glucose (substrate-switch) may improve contractile function in… Expand
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2008
2008
Antileukemic effects of the novel, mutant FLT3 inhibitor NVP-AST487: effects on PKC412-sensitive and -resistant FLT3-expressing cells.
An attractive target for therapeutic intervention is constitutively activated, mutant FLT3, which is expressed in a subpopulation… Expand
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Highly Cited
2003
Highly Cited
2003
1-[[(3-hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties.
Dipeptidyl peptidase IV (DPP-IV) inhibition has the potential to become a valuable therapy for type 2 diabetes. The synthesis and… Expand
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Highly Cited
2002
Highly Cited
2002
Long-term inhibition of dipeptidyl peptidase IV improves glucose tolerance and preserves islet function in mice.
OBJECTIVES Inhibitors of the glucagon-like peptide-1 (GLP-1)-degrading enzyme, dipeptidyl peptidase IV (DPPIV), are being… Expand
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Highly Cited
2002
Highly Cited
2002
Inhibition of dipeptidyl peptidase IV improves metabolic control over a 4-week study period in type 2 diabetes.
OBJECTIVE Glucagon-like peptide-1 (GLP-1) has been proposed as a new treatment modality for type 2 diabetes. To circumvent the… Expand
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