(Q44581055)

4 December 2017

title

Ab initio study of the binding of Trichostatin A (TSA) in the active site of histone deacetylase like protein (HDLP). (English)

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4 December 2017

1

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4 December 2017

author name string

Christian Van Alsenoy

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4 December 2017

Frank De Proft

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4 December 2017

José C Martins

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4 December 2017

Dirk Tourwé

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4 December 2017

Paul Geerlings

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4 December 2017

publication date

1 August 2003

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Organic and Biomolecular Chemistry

4 December 2017

published in

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4 December 2017

volume

1

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4 December 2017

issue

16

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4 December 2017

page(s)

2951-2957

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Histone deacetylase: a target for antiproliferative and antiprotozoal agents

4 December 2017

cites work

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Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells

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Histone deacetylases and cancer: causes and therapies

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Trichostatin A, a histone deacetylase inhibitor, suppresses collagen synthesis and prevents TGF-beta(1)-induced fibrogenesis in skin fibroblasts

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A histone deacetylase inhibitor, trichostatin A, suppresses myofibroblastic differentiation of rat hepatic stellate cells in primary culture

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Trichostatin A reverses skewed expression of CD154, interleukin-10, and interferon-gamma gene and protein expression in lupus T cells

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The antitumor histone deacetylase inhibitor suberoylanilide hydroxamic acid exhibits antiinflammatory properties via suppression of cytokines

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Histone deacetylase inhibitors reduce polyglutamine toxicity

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Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila

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Major phase I biotransformation pathways of Trichostatin a in rat hepatocytes and in rat and human liver microsomes

21 January 2018

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Inhibitors of human histone deacetylase: synthesis and enzyme and cellular activity of straight chain hydroxamates

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Second generation hybrid polar compounds are potent inducers of transformed cell differentiation.

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3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors

21 January 2018

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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

21 January 2018

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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

21 January 2018

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Amide analogues of TSA: synthesis, binding mode analysis and HDAC inhibition

21 January 2018

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Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

21 January 2018

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A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases.

21 January 2018

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Anti-tumour activity in vitro and in vivo of selective differentiating agents containing hydroxamate

21 January 2018

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A nucleophile activation dyad in ribonucleases. A combined X-ray crystallographic/ab initio quantum chemical study

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The Protein Data Bank

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The calculation of small molecular interactions by the differences of separate total energies. Some procedures with reduced errors

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The active site of a zinc-dependent metalloproteinase influences the computed pK(a) of ligands coordinated to the catalytic zinc ion.

21 January 2018

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Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94

21 January 2018

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Thermodynamic analysis of the binding of aromatic hydroxamic acid analogues to ferric horseradish peroxidase

21 January 2018

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Ab Initio Geometry Determinations of Proteins. 1. Crambin

21 January 2018

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21 January 2018

Identifiers

DOI

10.1039/B304707E

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4 December 2017

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