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alisertib
Known as:
Benzoic Acid, 4-((9-Chloro-7-(2-Fluoro-6-Methoxyphenyl)-5H-Pyrimido(5,4-d)(2)Benzazepin-2-yl)Amino)-2-Methoxy-
A second-generation, orally bioavailable, highly selective small molecule inhibitor of the serine/threonine protein kinase Aurora A kinase with…
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National Institutes of Health
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Related topics
Related topics
3 relations
Aurora Kinase A
NCIt Antineoplastic Agent Terminology
Broader (1)
MLN 8237
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2019
Highly Cited
2019
A Phase II Study of Alisertib in Children with Recurrent/Refractory Solid Tumors or Leukemia: Children's Oncology Group Phase I and Pilot Consortium (ADVL0921)
Y. Mossé
,
E. Fox
,
+13 authors
B. Weigel
Clinical Cancer Research
2019
Corpus ID: 73468436
Purpose: Aurora A kinase (AAK) plays an integral role in mitotic entry, DNA damage checkpoint recovery, and centrosome and…
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Highly Cited
2018
Highly Cited
2018
Phase II Trial of Alisertib in Combination with Irinotecan and Temozolomide for Patients with Relapsed or Refractory Neuroblastoma
S. DuBois
,
Y. Mossé
,
+26 authors
A. Marachelian
Clinical Cancer Research
2018
Corpus ID: 51955314
Purpose: In phase I testing, alisertib tablets with irinotecan and temozolomide showed significant antitumor activity in patients…
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Review
2018
Review
2018
Molecularly Targeted Therapy for Neuroblastoma
Emily G Greengard
Children
2018
Corpus ID: 53220225
Neuroblastoma is the most common extra-cranial solid tumor encountered in childhood and accounts for 15% of pediatric cancer…
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Highly Cited
2015
Highly Cited
2015
Phase II Intergroup Trial of Alisertib in Relapsed and Refractory Peripheral T-Cell Lymphoma and Transformed Mycosis Fungoides: SWOG 1108.
P. Barr
,
Hongli Li
,
+13 authors
J. Friedberg
Journal of Clinical Oncology
2015
Corpus ID: 29354510
PURPOSE Aurora A kinase (AAK) is upregulated in highly proliferative lymphomas, suggesting its potential as a therapeutic target…
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Highly Cited
2015
Highly Cited
2015
Alisertib is active as single agent in recurrent atypical teratoid rhabdoid tumors in 4 children.
C. Wetmore
,
J. Boyett
,
+4 authors
B. Orr
Neuro-Oncology
2015
Corpus ID: 19401400
BACKGROUND Aurora Kinase A (AURKA) encodes a protein that regulates the formation and stability of the mitotic spindle and is…
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Highly Cited
2015
Highly Cited
2015
The investigational Aurora kinase A inhibitor alisertib (MLN8237) induces cell cycle G2/M arrest, apoptosis, and autophagy via p38 MAPK and Akt/mTOR signaling pathways in human breast cancer cells
Jin-Ping Li
,
Yinxue Yang
,
+8 authors
Shufeng Zhou
Drug Design, Development and Therapy
2015
Corpus ID: 16817134
Alisertib (ALS) is an investigational potent Aurora A kinase inhibitor currently undergoing clinical trials for the treatment of…
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Review
2014
Review
2014
Recent advances in diagnosis and treatment of gliomas using chlorotoxin-based bioconjugates.
Yongjun Cheng
,
Jinhua Zhao
,
Wenli Qiao
,
Kai Chen
American Journal of Nuclear Medicine and…
2014
Corpus ID: 20978928
Malignant gliomas, especially glioblastoma multiforme, are the most widely distributed and deadliest brain tumors because of…
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Highly Cited
2012
Highly Cited
2012
Identification of Regulators of Polyploidization Presents Therapeutic Targets for Treatment of AMKL
Q. Wen
,
Benjamin H Goldenson
,
+45 authors
J. Crispino
Cell
2012
Corpus ID: 12117991
Highly Cited
2012
Highly Cited
2012
Phase I Study of Aurora A Kinase Inhibitor MLN8237 in Advanced Solid Tumors: Safety, Pharmacokinetics, Pharmacodynamics, and Bioavailability of Two Oral Formulations
E. Dees
,
Roger B. Cohen
,
+7 authors
J. Infante
Clinical Cancer Research
2012
Corpus ID: 39940242
Purpose: This phase I study evaluated the safety, pharmacokinetics, pharmacodynamics, and efficacy of the investigational oral…
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Highly Cited
2012
Highly Cited
2012
Targeting Aurora A kinase activity with the investigational agent alisertib increases the efficacy of cytarabine through a FOXO‐dependent mechanism
K. Kelly
,
S. Nawrocki
,
+6 authors
J. Carew
International Journal of Cancer
2012
Corpus ID: 30533717
Novel therapies are urgently needed to improve clinical outcomes for patients with acute myeloid leukemia (AML). The…
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