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3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-alkylamides as a new class of synthetic histone deacetylase inhibitors. 1. Design, synthesis, biological evaluation, and binding mode studies performed through three different docking procedures

artículo científico publicado en 2003

3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 2. Effect of pyrrole-C2 and/or -C4 substitutions on biological activity

artículo científico publicado en 2004

3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 3. Discovery of novel lead compounds through structure-based drug design and docking studies

artículo científico publicado en 2004

Antimalarial and antileishmanial activities of aroyl-pyrrolyl-hydroxyamides, a new class of histone deacetylase inhibitors

artículo científico publicado en 2004

GPR55: Current knowledge and future perspectives of a purported "Type-3" cannabinoid receptor

artículo científico publicado en 2010

Histone deacetylation in epigenetics: an attractive target for anticancer therapy

artículo científico publicado en 2005

In silico scaffold evaluation and solid phase approach to identify new gelatinase inhibitors ⬇️

artículo científico publicado el 13 de febrero de 2012

Structural bases for substrate and inhibitor recognition by matrix metalloproteinases

scientific article published on January 2008

Thiopyrophosphoantigens: solid-phase synthesis and in vitro characterization of a new class of Vgamma9 Vdelta2 T cells activators

artículo científico publicado en 2009

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