Protein-Protein Interaction Modulators for Epigenetic Therapies

被引:22
|
作者
Diaz-Eufracio, Barbara I. [1 ]
Jesus Naveja, J. [1 ,2 ]
Medina-Franco, Jose L. [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Quim, Mexico City, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Med, PECEM, Mexico City, DF, Mexico
关键词
ACUTE MYELOID-LEUKEMIA; BET BROMODOMAIN INHIBITION; PEPTIDE-BASED DRUGS; CHEMICAL SPACE; THERAPEUTIC TARGETS; MIMICKING PEPTIDE; CANCER-THERAPY; HISTONE H3; DISCOVERY; BINDING;
D O I
10.1016/bs.apcsb.2017.06.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Targeting protein-protein interactions (PPIs) is becoming an attractive approach for drug discovery. This is particularly true for difficult or emerging targets, such as epitargets that may be elusive to drugs that fall into the traditional chemical space. The chemical nature of the PPIs makes attractive the use of peptides or peptidomimetics to selectively modulate such interactions. Despite the fact peptide-based drug discovery has been challenging, the use of peptides as leads compounds for drug discovery is still a valid strategy. This chapter discusses the current status of PPIs in epigenetic drug discovery. A special emphasis is made on peptides and peptide-like compounds as potential drug candidates.
引用
收藏
页码:65 / 84
页数:20
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