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MK 2206
Known as:
Akt inhibitor MK2206
, MK-2206
, MK2206
An orally bioavailable allosteric inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity. Akt…
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Heterocyclic Compounds, 3-Ring
NCIt Antineoplastic Agent Terminology
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Exogenous hydrogen sulfide attenuates the development of diabetic cardiomyopathy via the FoxO1 pathway
Peng Ye
,
Yue Gu
,
+7 authors
Shaoliang Chen
Journal of Cellular Physiology
2018
Corpus ID: 51921187
Previous studies have suggested that exogenous hydrogen sulfide can alleviate the development of diabetic cardiomyopathy (DCM) by…
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2017
2017
MTA1 promotes epithelial to mesenchymal transition and metastasis in non-small-cell lung cancer
K. Ma
,
Yangwei Fan
,
+11 authors
Yinying Wu
OncoTarget
2017
Corpus ID: 27617648
The present study assessed the role of metastasis-associated protein 1 (MTA1) in epithelial to mesenchymal transition (EMT) and…
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2015
2015
Maslinic acid promotes synaptogenesis and axon growth via Akt/GSK-3β activation in cerebral ischemia model.
Yisong Qian
,
Menghao Huang
,
+7 authors
Hongbin Sun
European Journal of Pharmacology
2015
Corpus ID: 33763459
2015
2015
Adaptively randomized trial of neoadjuvant chemotherapy with or without the Akt inhibitor MK-2206: Graduation results from the I-SPY 2 Trial.
D. Tripathy
,
A. J. Chien
,
+16 authors
D. Yee
2015
Corpus ID: 79045520
524 Background: A key node of growth and survival signaling pathways is the Akt serine/threonine kinase that activates mTOR and…
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2014
2014
A phase I trial of MK‐2206 in children with refractory malignancies: A Children's Oncology Group study
M. Fouladi
,
J. Perentesis
,
+10 authors
S. Blaney
Pediatric Blood & Cancer
2014
Corpus ID: 25865707
We report results of a phase I trial designed to estimate the maximum tolerated dose (MTD), describe dose‐limiting toxicities…
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2014
2014
Nucleolin enhances internal ribosomal entry site (IRES)-mediated translation of Sp1 in tumorigenesis.
Chia-Yang Hung
,
Wen-Bin Yang
,
Shao-An Wang
,
T. Hsu
,
Wen-Chang Chang
,
J. Hung
Biochimica et Biophysica Acta
2014
Corpus ID: 46179951
2013
2013
AKT collaborates with ERG and Gata1s to dysregulate megakaryopoiesis and promote AMKL
M. Stankiewicz
,
J. Crispino
Leukemia
2013
Corpus ID: 5914907
The requirement that leukemic Gata1 mutations be present in cells harboring trisomy 21 led to the discovery that overexpression…
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2013
2013
Combination therapy using Notch and Akt inhibitors is effective for suppressing invasion but not proliferation in glioma cells
Rihua Jin
,
M. Nakada
,
+8 authors
J. Hamada
Neuroscience Letters
2013
Corpus ID: 19345384
2010
2010
First-in-class phase I trial of a selective Akt inhibitor, MK2206 (MK), evaluating alternate day (QOD) and once weekly (QW) doses in advanced cancer patients (pts) with evidence of target modulation…
T. Yap
,
A. Patnaik
,
+7 authors
A. Tolcher
2010
Corpus ID: 78162555
3009 Background: Akt mediates cell proliferation, survival, and angiogenesis and is deregulated in cancer. MK is a potent…
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2009
2009
Abstract #3714: In vitro and in vivo antitumor activities of MK-2206, a new allosteric Akt inhibitor
Wei Lu
,
D. Defeo-jones
,
+15 authors
B. Pan
2009
Corpus ID: 86650218
Aberrant activation of the serine/threonine kinase Akt, a central node of the PI3K pathway, has been found in a significant…
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