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Kinase Inhibitors [MoA]
Known as:
Kinase Inhibitors
National Institutes of Health
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Related topics
Related topics
11 relations
Cobimetinib
alectinib
idelalisib
kinase inhibitor
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Practical Recommendations for Therapeutic Drug Monitoring of Kinase Inhibitors in Oncology
R. Verheijen
,
Huixin Yu
,
J. Schellens
,
J. Beijnen
,
N. Steeghs
,
A. Huitema
Clinical pharmacology and therapy
2017
Corpus ID: 30295157
Despite the fact that pharmacokinetic exposure of kinase inhibitors (KIs) is highly variable and clear relationships exist…
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Highly Cited
2017
Highly Cited
2017
Novel Pieces for the Emerging Picture of Sulfoximines in Drug Discovery: Synthesis and Evaluation of Sulfoximine Analogues of Marketed Drugs and Advanced Clinical Candidates
J. A. Sirvent
,
U. Lücking
ChemMedChem
2017
Corpus ID: 11201696
Sulfoximines have gained considerable recognition as an important structural motif in drug discovery of late. In particular, the…
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Highly Cited
2017
Highly Cited
2017
Optimal sequencing of ibrutinib, idelalisib, and venetoclax in chronic lymphocytic leukemia: results from a multicenter study of 683 patients.
A. Mato
,
B. Hill
,
+26 authors
C. Nabhan
Annals of Oncology
2017
Corpus ID: 54562008
Background Ibrutinib, idelalisib, and venetoclax are approved for treating CLL patients in the United States. However, there is…
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Review
2016
Review
2016
Survival of patients with advanced metastatic melanoma: The impact of novel therapies.
S. Ugurel
,
J. Röhmel
,
+11 authors
C. Garbe
European Journal of Cancer
2016
Corpus ID: 11345567
Highly Cited
2016
Highly Cited
2016
High-content screening identifies kinase inhibitors that overcome venetoclax resistance in activated CLL cells.
S. Oppermann
,
J. Ylanko
,
+7 authors
D. Andrews
Blood
2016
Corpus ID: 8258392
Novel agents such as the Bcl-2 inhibitor venetoclax (ABT-199) are changing treatment paradigms for chronic lymphocytic leukemia…
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Review
2016
Review
2016
Deregulation of the protein phosphatase 2A, PP2A in cancer: complexity and therapeutic options
G. Grech
,
S. Baldacchino
,
+5 authors
C. Scerri
Tumor Biology
2016
Corpus ID: 24784814
The complexity of the phosphatase, PP2A, is being unravelled and current research is increasingly providing information on the…
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Highly Cited
2016
Highly Cited
2016
Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
Jun Zhang
,
Alec T. Salminen
,
+10 authors
Q. Shi
Archives of Toxicology
2016
Corpus ID: 4791687
The FDA has approved 31 small-molecule kinase inhibitors (KIs) for human use as of November 2016, with six having black box…
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Review
2016
Review
2016
Quinoxaline‐Based Scaffolds Targeting Tyrosine Kinases and Their Potential Anticancer Activity
Aliya M S El Newahie
,
Nasser S M Ismail
,
D. A. Abou El Ella
,
K. Abouzid
Archiv der Pharmazie
2016
Corpus ID: 26223493
Quinoxaline derivatives, also called benzopyrazines, are an important class of heterocyclic compounds. Quinoxalines have drawn…
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Review
2015
Review
2015
Aurora Kinase Inhibitors: Current Status and Outlook
V. Bavetsias
,
S. Linardopoulos
Frontiers in Oncology
2015
Corpus ID: 16143557
The Aurora kinase family comprises of cell cycle-regulated serine/threonine kinases important for mitosis. Their activity and…
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Review
2010
Review
2010
Why do kinase inhibitors cause cardiotoxicity and what can be done about it?
Hui Cheng
,
T. Force
Progress in cardiovascular diseases
2010
Corpus ID: 36570777
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