-
1
-
-
67349160499
-
HDAC expression and clinical prognosis in human malignancies
-
Weichert, W. (2009) HDAC expression and clinical prognosis in human malignancies. Cancer Lett. 280, 168-176
-
(2009)
Cancer Lett.
, vol.280
, pp. 168-176
-
-
Weichert, W.1
-
2
-
-
40849139208
-
Epigenetics in cancer
-
Esteller, M. (2008) Epigenetics in cancer. N. Engl. J. Med. 358, 1148-1159
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 1148-1159
-
-
Esteller, M.1
-
3
-
-
84860371953
-
Epigenetic protein families: A new frontier for drug discovery
-
Arrowsmith, C. H. et al. (2012) Epigenetic protein families: a new frontier for drug discovery. Nat. Rev. Drug Discov. 11, 384-400
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 384-400
-
-
Arrowsmith, C.H.1
-
4
-
-
70349311616
-
Histone acetyl transferases as emerging drug targets
-
Dekker, F. J. and Haisma, H. J. (2009) Histone acetyl transferases as emerging drug targets. Drug Discov. Today 14, 942-948
-
(2009)
Drug Discov. Today
, vol.14
, pp. 942-948
-
-
Dekker, F.J.1
Haisma, H.J.2
-
5
-
-
0037382681
-
Collaborative spirit of histone deacetylases in regulating chromatin structure and gene expression
-
Yang, X.-J. and Seto, E. (2003) Collaborative spirit of histone deacetylases in regulating chromatin structure and gene expression. Curr. Opin. Genet. Dev. 13, 143-153
-
(2003)
Curr. Opin. Genet. Dev.
, vol.13
, pp. 143-153
-
-
Yang, X.-J.1
Seto, E.2
-
6
-
-
33746992118
-
Substrate and functional diversity of lysine acetylation revealed by a proteomics survey
-
Kim, S. C. et al. (2006) Substrate and functional diversity of lysine acetylation revealed by a proteomics survey. Mol. Cell 23, 607-618
-
(2006)
Mol. Cell
, vol.23
, pp. 607-618
-
-
Kim, S.C.1
-
7
-
-
68949212379
-
Lysine acetylation targets protein complexes and coregulates major cellular functions
-
Choudhary, C. et al. (2009) Lysine acetylation targets protein complexes and coregulates major cellular functions. Science 325, 834-840
-
(2009)
Science
, vol.325
, pp. 834-840
-
-
Choudhary, C.1
-
9
-
-
56049090769
-
Acetylation of non-histone proteins modulates cellular signalling at multiple levels
-
Spange, S. et al. (2009) Acetylation of non-histone proteins modulates cellular signalling at multiple levels. Int. J. Biochem. Cell Biol. 41, 185-198
-
(2009)
Int. J. Biochem. Cell Biol.
, vol.41
, pp. 185-198
-
-
Spange, S.1
-
10
-
-
84874410182
-
Histone deacetylase inhibitors (HDACIs): Multitargeted anticancer agents
-
Ververis, K. et al. (2013) Histone deacetylase inhibitors (HDACIs): multitargeted anticancer agents. Biologics 7, 47-60
-
(2013)
Biologics
, vol.7
, pp. 47-60
-
-
Ververis, K.1
-
11
-
-
79959337199
-
Deacetylase inhibitors: Focus on non-histone targets and effects
-
Ocker, M. (2010) Deacetylase inhibitors: focus on non-histone targets and effects. World J. Biol. Chem. 1, 55-61
-
(2010)
World J. Biol. Chem.
, vol.1
, pp. 55-61
-
-
Ocker, M.1
-
12
-
-
84908688867
-
Combination of proteasome and class I HDAC inhibitors induces apoptosis of NPC cells through an HDAC6-independent ER stress-induced mechanism
-
Hui, K. F. and Chiang, A. K. S. (2014) Combination of proteasome and class I HDAC inhibitors induces apoptosis of NPC cells through an HDAC6-independent ER stress-induced mechanism. Int. J. Cancer 135, 2950-2961
-
(2014)
Int. J. Cancer
, vol.135
, pp. 2950-2961
-
-
Hui, K.F.1
Chiang, A.K.S.2
-
13
-
-
79959804516
-
Histone deacetylases as regulators of inflammation and immunity
-
Shakespear, M. R. et al. (2011) Histone deacetylases as regulators of inflammation and immunity. Trends Immunol. 32, 335-343
-
(2011)
Trends Immunol.
, vol.32
, pp. 335-343
-
-
Shakespear, M.R.1
-
14
-
-
84855875719
-
Therapeutic potential for HDAC inhibitors in the heart
-
McKinsey, T. A. (2012) Therapeutic potential for HDAC inhibitors in the heart. Annu. Rev. Pharmacol. Toxicol. 52, 303-319
-
(2012)
Annu. Rev. Pharmacol. Toxicol.
, vol.52
, pp. 303-319
-
-
McKinsey, T.A.1
-
15
-
-
79955622702
-
Epigenetic regulation of gene expression in physiological and pathological brain processes
-
Gräff, J. et al. (2011) Epigenetic regulation of gene expression in physiological and pathological brain processes. Physiol. Rev. 91, 603-649
-
(2011)
Physiol. Rev.
, vol.91
, pp. 603-649
-
-
Gräff, J.1
-
16
-
-
65449160927
-
Inhibition of histone deacetylases: A pharmacological approach to the treatment of non-cancer disorders
-
Wiech, N. L. et al. (2009) Inhibition of histone deacetylases: a pharmacological approach to the treatment of non-cancer disorders. Curr. Top. Med. Chem. 9, 257-271
-
(2009)
Curr. Top. Med. Chem.
, vol.9
, pp. 257-271
-
-
Wiech, N.L.1
-
17
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
Sjöblom, T. et al. (2006) The consensus coding sequences of human breast and colorectal cancers. Science 314, 268-274
-
(2006)
Science
, vol.314
, pp. 268-274
-
-
Sjöblom, T.1
-
18
-
-
33646354640
-
A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition
-
Ropero, S. et al. (2006) A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition. Nat. Genet. 38, 566-569
-
(2006)
Nat. Genet.
, vol.38
, pp. 566-569
-
-
Ropero, S.1
-
19
-
-
84912130076
-
Compromised structure and function of HDAC8 mutants identified in Cornelia de Lange Syndrome spectrum disorders
-
Decroos, C. et al. (2014) Compromised structure and function of HDAC8 mutants identified in Cornelia de Lange Syndrome spectrum disorders. ACS Chem. Biol. 9, 2157-2164
-
(2014)
ACS Chem. Biol.
, vol.9
, pp. 2157-2164
-
-
Decroos, C.1
-
20
-
-
0034596309
-
Histone deacetylase inhibitors: Inducers of differentiation or apoptosis of transformed cells
-
Marks, P. A. et al. (2000) Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J. Natl. Cancer Inst. 92, 1210-1216
-
(2000)
J. Natl. Cancer Inst.
, vol.92
, pp. 1210-1216
-
-
Marks, P.A.1
-
21
-
-
84869869682
-
HDAC inhibitor-based therapies: Can we interpret the code?
-
New, M. et al. (2012) HDAC inhibitor-based therapies: can we interpret the code? Mol. Oncol. 6, 637-656
-
(2012)
Mol. Oncol.
, vol.6
, pp. 637-656
-
-
New, M.1
-
23
-
-
84903581670
-
Targeting histone deacetylases for cancer therapy: From molecular mechanisms to clinical implications
-
Li, Z. and Zhu, W.-G. (2014) Targeting histone deacetylases for cancer therapy: from molecular mechanisms to clinical implications. Int. J. Biol. Sci. 10, 757-770
-
(2014)
Int. J. Biol. Sci.
, vol.10
, pp. 757-770
-
-
Li, Z.1
Zhu, W.-G.2
-
24
-
-
33748451151
-
Anticancer activities of histone deacetylase inhibitors
-
Bolden, J. E. et al. (2006) Anticancer activities of histone deacetylase inhibitors. Nat. Rev. Drug Discov. 5, 769-784
-
(2006)
Nat. Rev. Drug Discov.
, vol.5
, pp. 769-784
-
-
Bolden, J.E.1
-
25
-
-
84892942381
-
New and emerging HDAC inhibitors for cancer treatment
-
West, A. C. and Johnstone, R. W. (2014) New and emerging HDAC inhibitors for cancer treatment. J. Clin. Invest. 124, 30-39
-
(2014)
J. Clin. Invest.
, vol.124
, pp. 30-39
-
-
West, A.C.1
Johnstone, R.W.2
-
26
-
-
33847258674
-
Discovery and development of SAHA as an anticancer agent
-
Marks, P. A. (2007) Discovery and development of SAHA as an anticancer agent. Oncogene 26, 1351-1356
-
(2007)
Oncogene
, vol.26
, pp. 1351-1356
-
-
Marks, P.A.1
-
27
-
-
77954879663
-
Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma
-
Whittaker, S. J. et al. (2010) Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma. J. Clin. Oncol. 28, 4485-4491
-
(2010)
J. Clin. Oncol.
, vol.28
, pp. 4485-4491
-
-
Whittaker, S.J.1
-
28
-
-
84894109459
-
Romidepsin for peripheral T-cell lymphoma
-
Khot, A. et al. (2013) Romidepsin for peripheral T-cell lymphoma. Expert Rev. Hematol. 6, 351-359
-
(2013)
Expert Rev. Hematol.
, vol.6
, pp. 351-359
-
-
Khot, A.1
-
29
-
-
84928774345
-
Belinostat: First global approval
-
Poole, R. M. (2014) Belinostat: first global approval. Drugs 74, 1543-1554
-
(2014)
Drugs
, vol.74
, pp. 1543-1554
-
-
Poole, R.M.1
-
30
-
-
84914815183
-
Trend of histone deacetylase inhibitors in cancer therapy: Isoform selectivity or multitargeted strategy
-
Zhang, L. et al. (2015) Trend of histone deacetylase inhibitors in cancer therapy: isoform selectivity or multitargeted strategy. Med. Res. Rev. 35, 63-84
-
(2015)
Med. Res. Rev.
, vol.35
, pp. 63-84
-
-
Zhang, L.1
-
31
-
-
84896703864
-
Towards selective inhibition of histone deacetylase isoforms: What has been achieved, where we are and what will be next
-
Thaler, F. and Mercurio, C. (2014) Towards selective inhibition of histone deacetylase isoforms: what has been achieved, where we are and what will be next. ChemMedChem 9, 523-526
-
(2014)
ChemMedChem
, vol.9
, pp. 523-526
-
-
Thaler, F.1
Mercurio, C.2
-
32
-
-
80052653226
-
Therapeutic strategies to enhance the anticancer efficacy of histone deacetylase inhibitors
-
Miller, C. P. et al. (2011) Therapeutic strategies to enhance the anticancer efficacy of histone deacetylase inhibitors. J. Biomed. Biotechnol. 2011, 514261
-
(2011)
J. Biomed. Biotechnol.
, vol.2011
, pp. 514261
-
-
Miller, C.P.1
-
33
-
-
0034610367
-
Genomewide studies of histone deacetylase function in yeast
-
Bernstein, B. E. et al. (2000) Genomewide studies of histone deacetylase function in yeast. Proc. Natl. Acad. Sci. U. S. A. 97, 13708-13713
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 13708-13713
-
-
Bernstein, B.E.1
-
34
-
-
0037444803
-
Histone deacetylases (HDACs): Characterization of the classical HDAC family
-
De Ruijter, A. J. M. et al. (2003) Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem. J. 370, 737-749
-
(2003)
Biochem. J.
, vol.370
, pp. 737-749
-
-
De Ruijter, A.J.M.1
-
35
-
-
1842578986
-
Molecular evolution of the histone deacetylase family: Functional implications of phylogenetic analysis
-
Gregoretti, I. V. et al. (2004) Molecular evolution of the histone deacetylase family: functional implications of phylogenetic analysis. J. Mol. Biol. 338, 17-31
-
(2004)
J. Mol. Biol.
, vol.338
, pp. 17-31
-
-
Gregoretti, I.V.1
-
36
-
-
2942564591
-
Sirtuins: Sir2-related NAD-dependent protein deacetylases
-
North, B. J. and Verdin, E. (2004) Sirtuins: Sir2-related NAD-dependent protein deacetylases. Genome Biol. 5, 224
-
(2004)
Genome Biol.
, vol.5
, pp. 224
-
-
North, B.J.1
Verdin, E.2
-
37
-
-
77955355838
-
Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatinA. J
-
Butler, K. V. et al. (2010) Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatinA. J. Am. Chem. Soc. 132, 10842-10846
-
(2010)
Am. Chem. Soc.
, vol.132
, pp. 10842-10846
-
-
Butler, K.V.1
-
38
-
-
0024335390
-
Binding of D-phenylalanine and D-tyrosine to carboxypeptidase A
-
Christianson, D. W. et al. (1989) Binding of D-phenylalanine and D-tyrosine to carboxypeptidase A. J. Biol. Chem. 264, 12849-12853
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 12849-12853
-
-
Christianson, D.W.1
-
39
-
-
0015935205
-
The charge relay system in chymotrypsin and chymotrypsinogen
-
Fersht, A. R. and Sperling, J. (1973) The charge relay system in chymotrypsin and chymotrypsinogen. J. Mol. Biol. 74, 137-149
-
(1973)
J. Mol. Biol.
, vol.74
, pp. 137-149
-
-
Fersht, A.R.1
Sperling, J.2
-
40
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
Finnin, M. S. et al. (1999) Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors. Nature 401, 188-193
-
(1999)
Nature
, vol.401
, pp. 188-193
-
-
Finnin, M.S.1
-
41
-
-
19444379914
-
Theoretical study revealing the functioning of a novel combination of catalytic motifs in histone deacetylase
-
Vanommeslaeghe, K. et al. (2005) Theoretical study revealing the functioning of a novel combination of catalytic motifs in histone deacetylase. Bioorg. Med. Chem. 13, 3987-3992
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 3987-3992
-
-
Vanommeslaeghe, K.1
-
42
-
-
33646021957
-
Unexpected deacetylation mechanism suggested by a density functional theory QM/MM study of histone-deacetylase-like protein
-
Corminboeuf, C. et al. (2006) Unexpected deacetylation mechanism suggested by a density functional theory QM/MM study of histone-deacetylase-like protein. J. Am. Chem. Soc. 128, 4530-4531
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4530-4531
-
-
Corminboeuf, C.1
-
43
-
-
84891720942
-
Class I HDACs share a common mechanism of regulation by inositol phosphates
-
Millard, C. J. et al. (2013) Class I HDACs share a common mechanism of regulation by inositol phosphates. Mol. Cell 51, 57-67
-
(2013)
Mol. Cell
, vol.51
, pp. 57-67
-
-
Millard, C.J.1
-
44
-
-
77952100365
-
Exploration of the HDAC2 foot pocket: Synthesis and SAR of substituted N-(2-aminophenyl) benzamides
-
Bressi, J. C. et al. (2010) Exploration of the HDAC2 foot pocket: synthesis and SAR of substituted N-(2-aminophenyl) benzamides. Bioorg. Med. Chem. Lett. 20, 3142-3145
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 3142-3145
-
-
Bressi, J.C.1
-
45
-
-
84884188776
-
Histone deacetylase (HDAC) inhibitor kinetic rate constants correlate with cellular histone acetylation but not transcription and cell viability
-
Lauffer, B. E. L. et al. (2013) Histone deacetylase (HDAC) inhibitor kinetic rate constants correlate with cellular histone acetylation but not transcription and cell viability. J. Biol. Chem. 288, 26926-26943
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 26926-26943
-
-
Lauffer, B.E.L.1
-
46
-
-
84855984763
-
Structure of HDAC3 bound to co-repressor and inositol tetraphosphate
-
Watson, P. J. et al. (2012) Structure of HDAC3 bound to co-repressor and inositol tetraphosphate. Nature 481, 335-340
-
(2012)
Nature
, vol.481
, pp. 335-340
-
-
Watson, P.J.1
-
47
-
-
55549094833
-
Structural and functional analysis of the human HDAC4 catalytic domain reveals a regulatory structural zinc-binding domain
-
Bottomley, M. J. et al. (2008) Structural and functional analysis of the human HDAC4 catalytic domain reveals a regulatory structural zinc-binding domain. J. Biol. Chem. 283, 26694-26704
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 26694-26704
-
-
Bottomley, M.J.1
-
48
-
-
84891304904
-
Design, synthesis, and biological evaluation of potent and selective class iia histone deacetylase (HDAC) inhibitors as a potential therapy for Huntington's disease
-
Burli, R. W. et al. (2013) Design, synthesis, and biological evaluation of potent and selective class iia histone deacetylase (HDAC) inhibitors as a potential therapy for Huntington's disease. J. Med. Chem. 56, 9934-9954
-
(2013)
J. Med. Chem.
, vol.56
, pp. 9934-9954
-
-
Burli, R.W.1
-
49
-
-
45549095066
-
Human HDAC7 harbors a class IIa histone deacetylasespecific zinc binding motif and cryptic deacetylase activity
-
Schuetz, A. et al. (2008) Human HDAC7 harbors a class IIa histone deacetylasespecific zinc binding motif and cryptic deacetylase activity. J. Biol. Chem. 283, 11355-11363
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 11355-11363
-
-
Schuetz, A.1
-
50
-
-
84879092346
-
Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group
-
Lobera, M. et al. (2013) Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group. Nat. Chem. Biol. 9, 319-325
-
(2013)
Nat. Chem. Biol.
, vol.9
, pp. 319-325
-
-
Lobera, M.1
-
51
-
-
35548947488
-
Substrate binding to histone deacetylases as shown by the crystal structure of the HDAC8-substrate complex
-
Vannini, A. et al. (2007) Substrate binding to histone deacetylases as shown by the crystal structure of the HDAC8-substrate complex. EMBO Rep. 8, 879-884
-
(2007)
EMBO Rep.
, vol.8
, pp. 879-884
-
-
Vannini, A.1
-
52
-
-
3142562372
-
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
-
Somoza, J. R. et al. (2004) Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases. Structure 12, 1325-1334
-
(2004)
Structure
, vol.12
, pp. 1325-1334
-
-
Somoza, J.R.1
-
53
-
-
6344222799
-
Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor
-
Vannini, A. et al. (2004) Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor. Proc. Natl. Acad. Sci. U. S. A. 101, 15064-15069
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 15064-15069
-
-
Vannini, A.1
-
54
-
-
79960561626
-
Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors
-
Whitehead, L. et al. (2011) Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors. Bioorg. Med. Chem. 19, 4626-4634
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 4626-4634
-
-
Whitehead, L.1
-
55
-
-
77953664293
-
Structures of metal-substituted human histone deacetylase 8 provide mechanistic inferences on biological function
-
Dowling, D. P. et al. (2010) Structures of metal-substituted human histone deacetylase 8 provide mechanistic inferences on biological function. Biochemistry 49, 5048-5056
-
(2010)
Biochemistry
, vol.49
, pp. 5048-5056
-
-
Dowling, D.P.1
-
56
-
-
58149144730
-
Structural studies of human histone deacetylase 8 and its site-specific variants complexed with substrate and inhibitors
-
Dowling, D. P. et al. (2008) Structural studies of human histone deacetylase 8 and its site-specific variants complexed with substrate and inhibitors. Biochemistry 47, 13554-13563
-
(2008)
Biochemistry
, vol.47
, pp. 13554-13563
-
-
Dowling, D.P.1
-
57
-
-
80051599485
-
Structural basis of the antiproliferative activity of largazole, a depsipeptide inhibitorofthe histonedeacetylases. J. Am
-
Cole, K. E. et al. (2011) Structural basis of the antiproliferative activity of largazole, a depsipeptide inhibitorofthe histonedeacetylases. J. Am. Chem. Soc. 133, 12474-12477
-
(2011)
Chem. Soc.
, vol.133
, pp. 12474-12477
-
-
Cole, K.E.1
-
58
-
-
38949141196
-
Phenylalanine-containing hydroxamic acids as selective inhibitors of class IIb histone deacetylases (HDACs)
-
Schäfer, S. et al. (2008) Phenylalanine-containing hydroxamic acids as selective inhibitors of class IIb histone deacetylases (HDACs). Bioorg. Med. Chem. 16, 2011-2033
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 2011-2033
-
-
Schäfer, S.1
-
59
-
-
34249676838
-
Complex structure of a bacterial class 2 histone deacetylase homologue with a trifluoromethylketone inhibitor
-
Nielsen, T. K. et al. (2007) Complex structure of a bacterial class 2 histone deacetylase homologue with a trifluoromethylketone inhibitor. Acta Crystallogr. F 63, 270-273
-
(2007)
Acta Crystallogr. F
, vol.63
, pp. 270-273
-
-
Nielsen, T.K.1
-
60
-
-
27344457467
-
Crystal structure of a bacterial class 2 histone deacetylase homologue
-
Nielsen, T. K. et al. (2005) Crystal structure of a bacterial class 2 histone deacetylase homologue. J. Mol. Biol. 354, 107-120
-
(2005)
J. Mol. Biol.
, vol.354
, pp. 107-120
-
-
Nielsen, T.K.1
-
61
-
-
0032520953
-
Histone deacetylase activity of Rpd3 is important for transcriptional repression in vivo
-
Kadosh, D. and Struhl, K. (1998) Histone deacetylase activity of Rpd3 is important for transcriptional repression in vivo. Genes Dev. 12, 797-805
-
(1998)
Genes Dev.
, vol.12
, pp. 797-805
-
-
Kadosh, D.1
Struhl, K.2
-
62
-
-
0032584224
-
A role for histone deacetylase activity in HDAC1-mediated transcriptional repression
-
Hassig, C. A. et al. (1998) A role for histone deacetylase activity in HDAC1-mediated transcriptional repression. Proc. Natl. Acad. Sci. U. S. A. 95, 3519-3524
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 3519-3524
-
-
Hassig, C.A.1
-
63
-
-
36849004821
-
Unraveling the hidden catalytic activity of vertebrate class IIa histone deacetylases
-
Lahm, A. et al. (2007) Unraveling the hidden catalytic activity of vertebrate class IIa histone deacetylases. Proc. Natl. Acad. Sci. U. S. A. 104, 17335-17340
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 17335-17340
-
-
Lahm, A.1
-
64
-
-
33646548638
-
Catalytic activity and inhibition of human histone deacetylase 8 is dependent on the identity of the active site metal ion
-
Gantt, S. L. et al. (2006) Catalytic activity and inhibition of human histone deacetylase 8 is dependent on the identity of the active site metal ion. Biochemistry 45, 6170-6178
-
(2006)
Biochemistry
, vol.45
, pp. 6170-6178
-
-
Gantt, S.L.1
-
65
-
-
77949908961
-
Activation and inhibition of histone deacetylase 8 by monovalent cations
-
Gantt, S. L. et al. (2010) Activation and inhibition of histone deacetylase 8 by monovalent cations. J. Biol. Chem. 285, 6036-6043
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 6036-6043
-
-
Gantt, S.L.1
-
66
-
-
84906330653
-
Inhibition and mechanism of HDAC8 revisited
-
Chen, K. et al. (2014) Inhibition and mechanism of HDAC8 revisited. J. Am. Chem. Soc. 136, 11636-11643
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 11636-11643
-
-
Chen, K.1
-
67
-
-
58149089923
-
Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I histone deacetylases
-
Chou, C. J. et al. (2008) Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I histone deacetylases. J. Biol. Chem. 283, 35402-35409
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 35402-35409
-
-
Chou, C.J.1
-
68
-
-
77953139148
-
On the inhibition of histone deacetylase 8
-
Estiu, G. et al. (2010) On the inhibition of histone deacetylase 8. Bioorg. Med. Chem. 18, 4103-4110
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 4103-4110
-
-
Estiu, G.1
-
69
-
-
84906059833
-
Exploring the potential binding sites of some known HDAC inhibitors on some HDAC8 conformers by docking studies
-
Sixto-López, Y. et al. (2014) Exploring the potential binding sites of some known HDAC inhibitors on some HDAC8 conformers by docking studies. Appl. Biochem. Biotechnol. 173, 1907-1926
-
(2014)
Appl. Biochem. Biotechnol.
, vol.173
, pp. 1907-1926
-
-
Sixto-López, Y.1
-
70
-
-
43949130430
-
Structural origin of selectivity in class II-selective histone deacetylase inhibitors
-
Estiu, G. et al. (2008) Structural origin of selectivity in class II-selective histone deacetylase inhibitors. J. Med. Chem. 51, 2898-2906
-
(2008)
J. Med. Chem.
, vol.51
, pp. 2898-2906
-
-
Estiu, G.1
-
71
-
-
52449112167
-
Residues in the 11 A channel of histone deacetylase 1 promote catalytic activity: Implications for designing isoformselective histone deacetylase inhibitors
-
Weerasinghe, S. V. W. et al. (2008) Residues in the 11 A channel of histone deacetylase 1 promote catalytic activity: implications for designing isoformselective histone deacetylase inhibitors. J. Med. Chem. 51, 5542-5551
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5542-5551
-
-
Weerasinghe, S.V.W.1
-
72
-
-
0036161439
-
Enzymatic activity associated with class II HDACs is dependent on a multiprotein complex containing HDAC3 and SMRT/N-CoR
-
Fischle, W. et al. (2002) Enzymatic activity associated with class II HDACs is dependent on a multiprotein complex containing HDAC3 and SMRT/N-CoR. Mol. Cell 9, 45-57
-
(2002)
Mol. Cell
, vol.9
, pp. 45-57
-
-
Fischle, W.1
-
73
-
-
39749127166
-
The Rpd3/Hda1 family of lysine deacetylases: From bacteria and yeast to mice and men
-
Yang, X.-J. and Seto, E. (2008) The Rpd3/Hda1 family of lysine deacetylases: from bacteria and yeast to mice and men. Nat. Rev. Mol. Cell Biol. 9, 206-218
-
(2008)
Nat. Rev. Mol. Cell Biol.
, vol.9
, pp. 206-218
-
-
Yang, X.-J.1
Seto, E.2
-
74
-
-
84860257685
-
Roles of histone deacetylases in epigenetic regulation: Emerging paradigms from studies with inhibitors
-
Delcuve, G. P. et al. (2012) Roles of histone deacetylases in epigenetic regulation: emerging paradigms from studies with inhibitors. Clin. Epigenetics 4, 5
-
(2012)
Clin. Epigenetics
, vol.4
, pp. 5
-
-
Delcuve, G.P.1
-
75
-
-
0034685766
-
Cloning and characterization of a novel human class I histone deacetylase that functions as a transcription repressor
-
Hu, E. et al. (2000) Cloning and characterization of a novel human class I histone deacetylase that functions as a transcription repressor. J. Biol. Chem. 275, 15254-15264
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 15254-15264
-
-
Hu, E.1
-
76
-
-
43749109171
-
A novel histone deacetylase 8 (HDAC8)-specific inhibitor PCI-34051 induces apoptosis in T-cell lymphomas
-
Balasubramanian, S. et al. (2008) A novel histone deacetylase 8 (HDAC8)-specific inhibitor PCI-34051 induces apoptosis in T-cell lymphomas. Leukemia 22, 1026-1034
-
(2008)
Leukemia
, vol.22
, pp. 1026-1034
-
-
Balasubramanian, S.1
-
77
-
-
79953772739
-
Oxime amides as a novel zinc binding group in histone deacetylase inhibitors: Synthesis, biological activity, and computational evaluation
-
Botta, C. B. et al. (2011) Oxime amides as a novel zinc binding group in histone deacetylase inhibitors: synthesis, biological activity, and computational evaluation. J. Med. Chem. 54, 2165-2182
-
(2011)
J. Med. Chem.
, vol.54
, pp. 2165-2182
-
-
Botta, C.B.1
-
78
-
-
0023568296
-
In vivo characterization of hydroxamic acid inhibitors of 5-lipoxygenase
-
Summers, J. B. et al. (1987) In vivo characterization of hydroxamic acid inhibitors of 5-lipoxygenase. J. Med. Chem. 30, 2121-2126
-
(1987)
J. Med. Chem.
, vol.30
, pp. 2121-2126
-
-
Summers, J.B.1
-
79
-
-
34247860871
-
Vorinostat for treatment of cutaneous manifestations of advanced primary cutaneous T-cell lymphoma
-
Mann, B. S. et al. (2007) Vorinostat for treatment of cutaneous manifestations of advanced primary cutaneous T-cell lymphoma. Clin. Cancer Res. 13, 2318-2322
-
(2007)
Clin. Cancer Res.
, vol.13
, pp. 2318-2322
-
-
Mann, B.S.1
-
80
-
-
34447340903
-
Zinc binding in HDAC inhibitors: A DFT study
-
Wang, D. et al. (2007) Zinc binding in HDAC inhibitors: a DFT study. J. Org. Chem. 72, 5446-5449
-
(2007)
J. Org. Chem.
, vol.72
, pp. 5446-5449
-
-
Wang, D.1
-
81
-
-
0041317608
-
Ab initio study of the binding of Trichostatin A (TSA) in the active site of histone deacetylase like protein (HDLP)
-
Vanommeslaeghe, K. et al. (2003) Ab initio study of the binding of Trichostatin A (TSA) in the active site of histone deacetylase like protein (HDLP). Org. Biomol. Chem. 1, 2951-2957
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 2951-2957
-
-
Vanommeslaeghe, K.1
-
82
-
-
84961981250
-
DFT-based ranking of zinc-binding groups in histone deacetylase inhibitors
-
Vanommeslaeghe, K. et al. (2005) DFT-based ranking of zinc-binding groups in histone deacetylase inhibitors. Bioorg. Med. Chem. 13, 6070-6082
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 6070-6082
-
-
Vanommeslaeghe, K.1
-
83
-
-
84878064234
-
Computational exploration of zinc binding groups for HDAC inhibition
-
Chen, K. et al. (2013) Computational exploration of zinc binding groups for HDAC inhibition. J. Org. Chem. 78, 5051-5055
-
(2013)
J. Org. Chem.
, vol.78
, pp. 5051-5055
-
-
Chen, K.1
-
84
-
-
37849019672
-
Determination of the class and isoform selectivity of smallmolecule histone deacetylase inhibitors
-
Khan, N. et al. (2008) Determination of the class and isoform selectivity of smallmolecule histone deacetylase inhibitors. Biochem. J. 409, 581-589
-
(2008)
Biochem. J.
, vol.409
, pp. 581-589
-
-
Khan, N.1
-
85
-
-
2942545807
-
On the function of the 14 A long internal cavity of histone deacetylase-like protein: Implications for the design of histone deacetylase inhibitors
-
Wang, D.-F. et al. (2004) On the function of the 14 A long internal cavity of histone deacetylase-like protein: implications for the design of histone deacetylase inhibitors. J. Med. Chem. 47, 3409-3417
-
(2004)
J. Med. Chem.
, vol.47
, pp. 3409-3417
-
-
Wang, D.-F.1
-
86
-
-
84863126869
-
Exploring inhibitor release pathways in histone deacetylases using random acceleration molecular dynamics simulations
-
Kalyaanamoorthy, S. and Chen, Y.-P. P. (2012) Exploring inhibitor release pathways in histone deacetylases using random acceleration molecular dynamics simulations. J. Chem. Inf. Model. 52, 589-603
-
(2012)
J. Chem. Inf. Model.
, vol.52
, pp. 589-603
-
-
Kalyaanamoorthy, S.1
Chen, Y.-P.P.2
-
87
-
-
84894031215
-
Mutagenesis studies of the 14 Å internal cavity of histone deacetylase 1: Insights toward the acetate-escape hypothesis and selective inhibitor design
-
Wambua, M. K. et al. (2014) Mutagenesis studies of the 14 Å internal cavity of histone deacetylase 1: insights toward the acetate-escape hypothesis and selective inhibitor design. J. Med. Chem. 57, 642-650
-
(2014)
J. Med. Chem.
, vol.57
, pp. 642-650
-
-
Wambua, M.K.1
-
88
-
-
33744514787
-
Substrate and inhibitor specificity of class 1 and class 2 histone deacetylases
-
Hildmann, C. et al. (2006) Substrate and inhibitor specificity of class 1 and class 2 histone deacetylases. J. Biotechnol. 124, 258-270
-
(2006)
J. Biotechnol.
, vol.124
, pp. 258-270
-
-
Hildmann, C.1
-
89
-
-
0346725952
-
Negative regulation of histone deacetylase 8 activity by cyclic AMP-dependent protein kinase A
-
Lee, H. et al. (2004) Negative regulation of histone deacetylase 8 activity by cyclic AMP-dependent protein kinase A. Mol. Cell. Biol. 24, 765-773
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 765-773
-
-
Lee, H.1
-
90
-
-
79952486549
-
On the function of the internal cavity of histone deacetylase protein 8: R37 is a crucial residue for catalysis
-
Haider, S. et al. (2011) On the function of the internal cavity of histone deacetylase protein 8:R37 is a crucial residue for catalysis. Bioorg. Med. Chem. Lett. 21, 2129-2132
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 2129-2132
-
-
Haider, S.1
-
91
-
-
42049121320
-
2-Trifluoroacetylthiophenes, a novel series of potent and selective class II histone deacetylase inhibitors
-
Jones, P. et al. (2008) 2-Trifluoroacetylthiophenes, a novel series of potent and selective class II histone deacetylase inhibitors. Bioorg. Med. Chem. Lett. 18, 3456-3461
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 3456-3461
-
-
Jones, P.1
-
92
-
-
40849086606
-
Probing the elusive catalytic activity of vertebrate class IIa histone deacetylases
-
Jones, P. et al. (2008) Probing the elusive catalytic activity of vertebrate class IIa histone deacetylases. Bioorg. Med. Chem. Lett. 18, 1814-1819
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 1814-1819
-
-
Jones, P.1
-
93
-
-
55549093722
-
2-Trifluoroacetylthiophene oxadiazoles as potent and selective class II human histone deacetylase inhibitors
-
Muraglia, E. et al. (2008) 2-Trifluoroacetylthiophene oxadiazoles as potent and selective class II human histone deacetylase inhibitors. Bioorg. Med. Chem. Lett. 18, 6083-6087
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 6083-6087
-
-
Muraglia, E.1
|