List of works - Peter Loidl

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

scientific article published on February 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

scientific article published on February 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

scientific article published on March 2004

A new amidohydrolase from Bordetella or Alcaligenes strain FB188 with similarities to histone deacetylases

scientific article

A novel motif in fungal class 1 histone deacetylases is essential for growth and development of Aspergillus

scientific article

A plant dialect of the histone language

scientific article published on February 2004

Acetylation of UBF changes during the cell cycle and regulates the interaction of UBF with RNA polymerase I.

scientific article

Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation

scientific article published in April 2002

Cell cycle dependent role of HDAC1 for proliferation control through modulating ribosomal DNA transcription

scientific article published on 2 May 2008

Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides

scientific article published in May 2005

Discovery of (Aryloxopropenyl)pyrrolyl Hydroxyamides as Selective Inhibitors of Class IIa Histone Deacetylase Homologue HD1-A ⬇️

scientific article published on 01 November 2003

HdaA, a major class 2 histone deacetylase of Aspergillus nidulans, affects growth under conditions of oxidative stress.

scientific article

Histone deacetylases in fungi: novel members, new facts

scientific article

Histone methyltransferases in Aspergillus nidulans: evidence for a novel enzyme with a unique substrate specificity.

scientific article

Histone modifications and chromatin dynamics: a focus on filamentous fungi

scientific article published on 23 January 2008

In Vitro Phosphorylation and Acetylation of the Murine Pocket Protein Rb2/p130 ⬇️

scientific article published on September 24, 2012

Mad1 function in cell proliferation and transcriptional repression is antagonized by cyclin E/CDK2.

scientific article published on 18 February 2005

Molecular identification of PpHDAC1, the first histone deacetylase fron the slime mold Physarum polycephalum.

scientific article published in January 2002

Novel insights into the functional role of three protein arginine methyltransferases in Aspergillus nidulans

scientific article published on 23 March 2010

Regulation and processing of maize histone deacetylase Hda1 by limited proteolysis

scientific article published in August 2003

Structure-activity relationships on phenylalanine-containing inhibitors of histone deacetylase: in vitro enzyme inhibition, induction of differentiation, and inhibition of proliferation in Friend leukemic cells.

scientific article

List of works by Peter Loidl

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

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

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

A new amidohydrolase from Bordetella or Alcaligenes strain FB188 with similarities to histone deacetylases

A novel motif in fungal class 1 histone deacetylases is essential for growth and development of Aspergillus

A plant dialect of the histone language

Acetylation of UBF changes during the cell cycle and regulates the interaction of UBF with RNA polymerase I.

Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation

Cell cycle dependent role of HDAC1 for proliferation control through modulating ribosomal DNA transcription

Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides

Discovery of (Aryloxopropenyl)pyrrolyl Hydroxyamides as Selective Inhibitors of Class IIa Histone Deacetylase Homologue HD1-A ⬇️

HdaA, a major class 2 histone deacetylase of Aspergillus nidulans, affects growth under conditions of oxidative stress.

Histone deacetylases in fungi: novel members, new facts

Histone methyltransferases in Aspergillus nidulans: evidence for a novel enzyme with a unique substrate specificity.

Histone modifications and chromatin dynamics: a focus on filamentous fungi

In Vitro Phosphorylation and Acetylation of the Murine Pocket Protein Rb2/p130 ⬇️

Mad1 function in cell proliferation and transcriptional repression is antagonized by cyclin E/CDK2.

Molecular identification of PpHDAC1, the first histone deacetylase fron the slime mold Physarum polycephalum.

Novel insights into the functional role of three protein arginine methyltransferases in Aspergillus nidulans

Regulation and processing of maize histone deacetylase Hda1 by limited proteolysis

Structure-activity relationships on phenylalanine-containing inhibitors of histone deacetylase: in vitro enzyme inhibition, induction of differentiation, and inhibition of proliferation in Friend leukemic cells.