Title : Docking and QSAR Studies of Aryl-valproic Acid Derivatives to Identify Antiproliferative Agents Targeting the HDAC8.

Pub. Date : 2017

PMID : 27774878






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 BACKGROUND: Histone deacetylase 8 (HDAC8) is a plausible target for the development of novel anticancer drugs using a metal-chelating group and hydrophobic moieties as pharmacophores. Metals histone deacetylase 8 Homo sapiens
2 BACKGROUND: Histone deacetylase 8 (HDAC8) is a plausible target for the development of novel anticancer drugs using a metal-chelating group and hydrophobic moieties as pharmacophores. Metals histone deacetylase 8 Homo sapiens