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pracinostat

Known as: 2-propenamide, 3-(2-butyl-1-(2-(diethylamino)ethyl)-1h-benzimidazol-5-yl)-N-hydroxy-, (2E)-, kaempferol 3-o-beta-d-(6-E-P-coumaroylglucoside) 
An orally available, small-molecule histone deacetylase (HDAC) inhibitor with potential antineoplastic activity. Pracinostat inhibits HDACs, which… 
National Institutes of Health

Papers overview

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2020
2020
7556Background: Hypomethylating agents (HMA), such as azacitidine (AZA), are the standard of care for patients (pts) with higher… 
Review
2019
Review
2019
Histone deacetylases (HDACs) are common targets for cancer therapy as they are expressed in many forms of cancers; several… 
2019
2019
Background: Relapsed/Refractory AML (RR-AML) represents an area in urgent need for new treatments, particularly among patients… 
2019
2019
AIM AND OBJECTIVE Mantle cell lymphoma (MCL) is typically an aggressive and rare disease with poor prognosis, therefore new… 
2019
2019
Background: AML is associated with poor survival rates in patients ineligible for IC or stem cell transplant due to advanced age… 
2018
2018
2018
Introduction: Higher risk MDS is a serious disease associated with poor survival with hypomethylating agents (HMAs) the… 
2017
2017
Chronic myeloid leukemia (CML) treatment has been improved by tyrosine kinase inhibitors (TKIs) such as imatinib mesylate (IM… 
Review
2016
Review
2016
Background: Pracinostat, a potent oral Class I, II, IV histone deacetylase (HDAC) inhibitor, exhibited modest single-agent… 
2014
2014
Background: Pracinostat is a potent oral inhibitor of histone deacetylases (HDAC’s), selective for class I, II and IV isoforms…