Hydroxamic acid derivatives are potential histone deacetylase inhibitors, and several hydroxamic acidbased histone deacetylase inhibitors have already been used clinically as potent anticancer agents, so hydroxamic acid derivatives are useful scaffolds for the development of novel anticancer agents. Hybridization of hydroxamic acid moiety with other anticancer pharmacophores can overcome drug resistance and improve the specificity, so rational design of hydroxamic acid hybrids may provide valuable therapeutic interventions for the treatment of cancers. The purpose of the present review article is to update the current developments in hydroxamic acid hybrids with an emphasis on anticancer activity, structure-activity relationships, and mechanisms of action. (C) 2020 Elsevier Masson SAS. All rights reserved.
机构:
Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Biol Reprod Dr Carlos Gual Castro, Ciudad De Mexico 14080, MexicoUniv Guanajuato, Dept Quim, Guanajuato 36050, Gto, Mexico
Ordaz-Rosado, David
Santos-Martinez, Nancy
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Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Biol Reprod Dr Carlos Gual Castro, Ciudad De Mexico 14080, MexicoUniv Guanajuato, Dept Quim, Guanajuato 36050, Gto, Mexico
Santos-Martinez, Nancy
Garcia-Becerra, Rocio
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Univ Nacl Autonoma Mexico, Inst Invest Biomed, Dept Biol Mol & Biotecnol, Ciudad De Mexico 04510, MexicoUniv Guanajuato, Dept Quim, Guanajuato 36050, Gto, Mexico