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rigosertib

Known as: RIGOSERTIB SODIUM 
A synthetic benzyl styryl sulfone analogue with potential antineoplastic activity. Polo-like kinase 1 inhibitor ON 01910.Na inhibits polo-like… 
National Institutes of Health

Papers overview

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2019
2019
Aberrant signaling triggered by oncogenic or hyperactive RAS proteins contributes to the malignant phenotypes in a significant… 
2018
2018
Background: AZA is first line therapy for pts with HR-MDS with an overall response rate (ORR) between 35 and 60% in various… 
Review
2017
Review
2017
Abstract Background: Prognosis of advanced pancreatic cancer is dismal and the novel targeted therapies, albeit successfully used… 
2016
2016
ABSTRACT Introduction: Therapeutic options for myelodysplastic syndromes (MDS) are limited to hypomethylating agents (HMA) and… 
2016
2016
Background: Based on a model suggesting leukemia can be driven by combined effect of mutations in an epigenetic gene (DNMT3) and… 
2014
2014
![Graphic][1] Background: No approved treatment options are available to HR-MDS pts after HMA therapy. Study 04-21 (“ONTIME… 
2013
2013
The dual pathway inhibitor rigosertib inhibits phosphoinositide 3-kinase (PI3K) pathway activation as well as polo-like kinase 1… 
2013
2013
![Graphic][1] Rigosertib, a novel orally bioavailable small molecule inhibitor of PI3-Kinase and PLK1 pathways, was tested in a… 
2011
2011
Abstract 3822 Rigosertib is a multi-kinase inhibitor that selectively induces mitotic arrest leading to apoptosis in cancer cells…