Title : Enantioselective apoptosis induction in histiocytic lymphoma cells and acute promyelocytic leukemia cells.

Pub. Date : 2013 Feb

PMID : 23010695






4 Functional Relationships(s)
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1 The aim of this study was to identify valproic acid (VPA) analogs with a broad spectrum of anti-cancer activities and an increased apoptosis-inducing potential compared with the parent VPA, which is enrolled as histone deacetylase (HDAC) inhibitor in a large number of clinical trials. Valproic Acid histone deacetylase 9 Homo sapiens
2 The aim of this study was to identify valproic acid (VPA) analogs with a broad spectrum of anti-cancer activities and an increased apoptosis-inducing potential compared with the parent VPA, which is enrolled as histone deacetylase (HDAC) inhibitor in a large number of clinical trials. Valproic Acid histone deacetylase 9 Homo sapiens
3 The aim of this study was to identify valproic acid (VPA) analogs with a broad spectrum of anti-cancer activities and an increased apoptosis-inducing potential compared with the parent VPA, which is enrolled as histone deacetylase (HDAC) inhibitor in a large number of clinical trials. Valproic Acid histone deacetylase 9 Homo sapiens
4 The aim of this study was to identify valproic acid (VPA) analogs with a broad spectrum of anti-cancer activities and an increased apoptosis-inducing potential compared with the parent VPA, which is enrolled as histone deacetylase (HDAC) inhibitor in a large number of clinical trials. Valproic Acid histone deacetylase 9 Homo sapiens