ABSTRACT
Histone deacetylase 11 (HDAC11), a member of the HDAC family, has emerged as a critical regulator in numerous physiological as well as pathological processes. Due to its diverse roles, HDAC11 has been a focal point of research in recent times. Different non-selective inhibitors are already approved, and research is going on to find selective HDAC11 inhibitors. The objective of this review is to comprehensively explore the role of HDAC11 as a pivotal regulator in a multitude of physiological and pathological processes. It aims to delve into the intricate details of HDAC11's structural and functional aspects, elucidating its molecular interactions and implications in different disease contexts. With a primary focus on elucidating the structure-activity relationships (SARs) of HDAC11 inhibitors, this review also aims to provide a holistic understanding of how its molecular architecture influences its inhibition. Additionally, by integrating both established knowledge and recent research, the review seeks to contribute novel insights into the potential therapeutic applications of HDAC11 inhibitors. Overall, the scope of this review spans from fundamental research elucidating the complexities of HDAC11 biology to the potential of targeting HDAC11 in therapeutic interventions.
Subject(s)
Drug Design , Epigenesis, Genetic , Histone Deacetylase Inhibitors , Histone Deacetylases , Humans , Histone Deacetylases/metabolism , Histone Deacetylases/chemistry , Histone Deacetylases/genetics , Histone Deacetylase Inhibitors/chemistry , Histone Deacetylase Inhibitors/pharmacology , Animals , Epigenesis, Genetic/drug effects , Structure-Activity RelationshipABSTRACT
New Rh (1) and Ir (2) complexes of an N-heterocyclic carbene (NHC) featuring a terthiophene backbone were synthesized. Single crystal X-ray diffraction studies of 1 and 2 at 100 K and 298 K respectively, revealed two enantiotropic polymorphic phases with similar lattice parameters for each compound. The transition temperature between two crystalline forms for each compound was determined by measuring the percentage of reflections with a different space group ranging from 100 K to 298 K. Both 1 and 2 were also found to catalyze the hydrogen transfer reaction. The conducting metallopolymers poly-1 and poly-2 were synthesized from oxidative electropolymerization of 1 and 2, respectively, in CH2Cl2 electrolyte solution on indium tin oxide-(ITO) coated glass. The electrochromic properties of synthesized conducting metallopolymers were studied by UV-vis-NIR spectroelectrochemistry.
