In silico studies on modified hydroxamic acid and valporic acid as potential inhibitors for HDAC2
Histone deacetylases2, Class 1 HDAC family are emerged as an important therapeutic target for the treatment of various cancers. HDAC2 inhibitors are potent anti-cancer agents. Two inhibitors of HDAC2 are hydroxamic acid and valporic acid which are potent inducers of growth arrest, differentiation, a...
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Bangladesh Pharmacological Society,
2013-07-01T00:00:00Z.
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A1234.567 |
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