Lista de obras - Jelena Melesina - Dominio Público Uruguay

2-Benzazolyl-4-Piperazin-1-Ylsulfonylbenzenecarbohydroxamic Acids as Novel Selective Histone Deacetylase-6 Inhibitors with Antiproliferative Activity

artículo científico publicado en 2015

A Novel Class of Schistosoma mansoni Histone Deacetylase 8 (HDAC8) Inhibitors Identified by Structure-Based Virtual Screening and In Vitro Testing.

artículo científico publicado en 2018

Carbamates as Potential Prodrugs and a New Warhead for HDAC Inhibition

artículo científico publicado en 2018

Characterization of histone deacetylase 8 (HDAC8) selective inhibition reveals specific active site structural and functional determinants

article

Chiral Pool Synthesis, Biological Evaluation and Molecular Docking Studies of C-Furanosidic LpxC Inhibitors

scientific article published on 12 March 2019

Design of selective histone deacetylase inhibitors: rethinking classical pharmacophore

artículo científico publicado en 2018

Discovery of inhibitors of Schistosoma mansoni HDAC8 by combining homology modeling, virtual screening, and in vitro validation

artículo científico publicado en 2014

Evolutionary relationships among protein lysine deacetylases of parasites causing neglected diseases

artículo científico publicado en 2017

Homology modeling of parasite histone deacetylases to guide the structure-based design of selective inhibitors

artículo científico publicado en 2015

Isoform-selective HDAC1/6/8 inhibitors with an imidazo-ketopiperazine cap containing stereochemical diversity

artículo científico publicado en 2018

Isophthalic Acid-Based HDAC Inhibitors as Potent Inhibitors of HDAC8 from Schistosoma mansoni.

artículo científico publicado en 2017

Molecular basis for the antiparasitic activity of a mercaptoacetamide derivative that inhibits histone deacetylase 8 (HDAC8) from the human pathogen schistosoma mansoni

artículo científico publicado en 2014

Proline-based hydroxamates targeting the zinc-dependent deacetylase LpxC: Synthesis, antibacterial properties, and docking studies

artículo científico publicado en 2019

Structure-Based Design and Biological Characterization of Selective Histone Deacetylase 8 (HDAC8) Inhibitors with Anti-Neuroblastoma Activity

artículo científico publicado en 2017

Structure-Based Design and Synthesis of Novel Inhibitors Targeting HDAC8 from Schistosoma mansoni for the Treatment of Schistosomiasis

artículo científico publicado en 2016

Synthesis and Biological Investigation of Oxazole Hydroxamates as Highly Selective Histone Deacetylase 6 (HDAC6) Inhibitors

artículo científico publicado en 2015

Synthesis and biochemical evaluation of two novel N-hydroxyalkylated cyclosporin A analogs

artículo científico publicado en 2018

Synthesis and biological evaluation of enantiomerically pure glyceric acid derivatives as LpxC inhibitors

artículo científico publicado en 2016

Synthesis, Crystallization Studies, and in vitro Characterization of Cinnamic Acid Derivatives as Sm HDAC8 Inhibitors for the Treatment of Schistosomiasis

artículo científico publicado en 2018

Synthesis, biological evaluation and molecular docking studies of benzyloxyacetohydroxamic acids as LpxC inhibitors

artículo científico publicado en 2014

Targeting histone deacetylase 8 as a therapeutic approach to cancer and neurodegenerative diseases

artículo científico publicado en 2016

Lista de obras de Jelena Melesina

2-Benzazolyl-4-Piperazin-1-Ylsulfonylbenzenecarbohydroxamic Acids as Novel Selective Histone Deacetylase-6 Inhibitors with Antiproliferative Activity

A Novel Class of Schistosoma mansoni Histone Deacetylase 8 (HDAC8) Inhibitors Identified by Structure-Based Virtual Screening and In Vitro Testing.

Carbamates as Potential Prodrugs and a New Warhead for HDAC Inhibition

Characterization of histone deacetylase 8 (HDAC8) selective inhibition reveals specific active site structural and functional determinants

Chiral Pool Synthesis, Biological Evaluation and Molecular Docking Studies of C-Furanosidic LpxC Inhibitors

Design of selective histone deacetylase inhibitors: rethinking classical pharmacophore

Discovery of inhibitors of Schistosoma mansoni HDAC8 by combining homology modeling, virtual screening, and in vitro validation

Evolutionary relationships among protein lysine deacetylases of parasites causing neglected diseases

Homology modeling of parasite histone deacetylases to guide the structure-based design of selective inhibitors

Isoform-selective HDAC1/6/8 inhibitors with an imidazo-ketopiperazine cap containing stereochemical diversity

Isophthalic Acid-Based HDAC Inhibitors as Potent Inhibitors of HDAC8 from Schistosoma mansoni.

Molecular basis for the antiparasitic activity of a mercaptoacetamide derivative that inhibits histone deacetylase 8 (HDAC8) from the human pathogen schistosoma mansoni

Proline-based hydroxamates targeting the zinc-dependent deacetylase LpxC: Synthesis, antibacterial properties, and docking studies

Structure-Based Design and Biological Characterization of Selective Histone Deacetylase 8 (HDAC8) Inhibitors with Anti-Neuroblastoma Activity

Structure-Based Design and Synthesis of Novel Inhibitors Targeting HDAC8 from Schistosoma mansoni for the Treatment of Schistosomiasis

Synthesis and Biological Investigation of Oxazole Hydroxamates as Highly Selective Histone Deacetylase 6 (HDAC6) Inhibitors

Synthesis and biochemical evaluation of two novel N-hydroxyalkylated cyclosporin A analogs

Synthesis and biological evaluation of enantiomerically pure glyceric acid derivatives as LpxC inhibitors

Synthesis, Crystallization Studies, and in vitro Characterization of Cinnamic Acid Derivatives as Sm HDAC8 Inhibitors for the Treatment of Schistosomiasis

Synthesis, biological evaluation and molecular docking studies of benzyloxyacetohydroxamic acids as LpxC inhibitors

Targeting histone deacetylase 8 as a therapeutic approach to cancer and neurodegenerative diseases