-
1
-
-
0033569641
-
Epigenetics: Regulation through repression
-
Wolffe, A.P.; Matzke, M.A. Epigenetics: Regulation through repression. Science, 1999, 286, 481-486.
-
(1999)
Science
, vol.286
, pp. 481-486
-
-
Wolffe, A.P.1
Matzke, M.A.2
-
2
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks, P.A.; Rifkind, R.A.; Richon, V.M.; Breslow, R.; Miller, T.; Kelly, W.K. Histone deacetylases and cancer: Causes and therapies. Nat. Rev. Cancer, 2001, 1, 194-202. (Pubitemid 33741894)
-
(2001)
Nature Reviews Cancer
, vol.1
, Issue.3
, pp. 194-202
-
-
Marks, P.A.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
3
-
-
34248329903
-
Review: Recent clinical trials in epigenetic therapy
-
Oki, Y.; Issa, J.P. Review: Recent clinical trials in epigenetic therapy. Rev. Recent Clin. Trials, 2006, 1, 169-182.
-
(2006)
Rev. Recent Clin. Trials
, vol.1
, pp. 169-182
-
-
Oki, Y.1
Issa, J.P.2
-
4
-
-
67349222049
-
Histone deacetylase inhibitors as anti-neoplastic agents
-
Batty, N.; Malouf, G.G.; Issa J.P. Histone deacetylase inhibitors as anti-neoplastic agents. Cancer Lett., 2009, 280, 192-200.
-
(2009)
Cancer Lett.
, vol.280
, pp. 192-200
-
-
Batty, N.1
Malouf, G.G.2
Issa, J.P.3
-
5
-
-
50349086621
-
The potential role of histone deacetylase inhibitors in the treatment of non-small-cell lung cancer
-
Cesare, G.; Antonio, R.; Paolo, M. The potential role of histone deacetylase inhibitors in the treatment of non-small-cell lung cancer. Critical Rev. Oncol./Hematol., 2008, 68, 29-36.
-
(2008)
Critical Rev. Oncol./Hematol.
, vol.68
, pp. 29-36
-
-
Cesare, G.1
Antonio, R.2
Paolo, M.3
-
6
-
-
0033561497
-
Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase
-
DOI 10.1038/sj.onc.1202564
-
Kim, Y.B.; Lee, K.H.; Sugita, K.; Yoshida, M.; Horinouchi, S. Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase. Oncogene, 1999, 18, 2461-2470. (Pubitemid 29206159)
-
(1999)
Oncogene
, vol.18
, Issue.15
, pp. 2461-2470
-
-
Kim, Y.B.1
Lee, K.-H.2
Sugita, K.3
Yoshida, M.4
Horinouchi, S.5
-
7
-
-
0035024737
-
Histone deacetylase: A target for antiproliferative and antiprotozoal agents
-
Meinke, P.T.; Liberator, P. Histone deacetylase: A target for antiproliferative and antiprotozoal agents. Curr. Med. Chem., 2001, 8, 211-235. (Pubitemid 32416448)
-
(2001)
Current Medicinal Chemistry
, vol.8
, Issue.2
, pp. 211-235
-
-
Meinke, P.T.1
Liberator, P.2
-
8
-
-
78650196313
-
Class of cytodifferentiating agents and histone deacetylase inhibitors, and method of use thereof
-
6511990-B1
-
Breslow, R.; Belvedere, S.; Gershell, L.; Miller, T.A.; Marks, P.A.; Richon, V.M.; Rifkind, R. Class of cytodifferentiating agents and histone deacetylase inhibitors, and method of use thereof. Patent Application US, 6511990-B1, 2003.
-
(2003)
Patent Application US
-
-
Breslow, R.1
Belvedere, S.2
Gershell, L.3
Miller, T.A.4
Marks, P.A.5
Richon, V.M.6
Rifkind, R.7
-
9
-
-
21244464349
-
Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer
-
DOI 10.1200/JCO.2005.14.167
-
Kelly, W.K.; Richon V.M.; O'Connor, O.; Curley, T.; MacGregor, C.B.; Tong, W.; Klang, M.; Schwartz, L.; Richardson, S.; Rosa, E.; Drobnjak, M.; Cordon, C.C.; Chiao, J.H.; Rifkind, R.; Marks, P.A.; Scher, H. Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J. Clin. Oncol., 2005, 23, 3923-3931. (Pubitemid 46218695)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.17
, pp. 3923-3931
-
-
Kelly, W.K.1
O'Connor, O.A.2
Krug, L.M.3
Chiao, J.H.4
Heaney, M.5
Curley, T.6
MacGregore-Cortelli, B.7
Tong, W.8
Secrist, J.P.9
Schwartz, L.10
Richardson, S.11
Chu, E.12
Olgac, S.13
Marks, P.A.14
Scher, H.15
Richon, V.M.16
-
10
-
-
34447509697
-
Vorinostat: A new oral histone deacetylase inhibitor approved for cutaneous T-cell lymphoma
-
DOI 10.1517/13543784.16.7.1111
-
Duvic, M.; Vu, J. Vorinostat: A new oral histone deacetylase inhibitor approved for cutaneous T-cell lymphoma. Expert Opin. Invest. Drugs, 2007, 16, 1111-1120. (Pubitemid 47074165)
-
(2007)
Expert Opinion on Investigational Drugs
, vol.16
, Issue.7
, pp. 1111-1120
-
-
Duvic, M.1
Vu, J.2
-
11
-
-
34548853387
-
Design and synthesis of thiazole-5- hydroxamic acids as novel histone deacetylase inhibitors
-
Sampath, K.A.; John, S.; Ward, R.D.; Brokx; Trisha, D.; Mark, R.B.; Dinesh, V.P.; Xiao, Y.X. Design and synthesis of thiazole-5- hydroxamic acids as novel histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 5995-5999.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 5995-5999
-
-
Sampath, K.A.1
John, S.2
Ward, R.D.3
Brokx4
Trisha, D.5
Mark, R.B.6
Dinesh, V.P.7
Xiao, Y.X.8
-
12
-
-
38749090156
-
Design and synthesis of 4-[(s-triazin-2-ylamino)methyl]-N-(2-aminophenyl) -benzamides and their analogues as a novel class of histone deacetylase inhibitors
-
DOI 10.1016/j.bmcl.2007.12.009, PII S0960894X07014539
-
Paquin,I.; Raeppel, S.; Leit, S.; Gaudette, F.; Zhou, N.; Moradei, O.; Saavedra, O.; Bernstein, N.; Raeppel, F.; Bouchain, G.; Frechette, S.; Woo, S.H.; Vaisburg, A.; Fournel, M.; Kalita, A.; Robert, M-F.; Lu, A.; Trachy-Bourget, M-C.; Yan, P.T.; Liu, J.; Rahil, J.; MacLeod, A.R.; Besterman, J.M.; Li, Z.; Delorme, D. Design and synthesis of 4-[(s-triazin-2-ylamino) methyl]-N-(2-aminophenyl)- benzamides and their analogues as a novel class of histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 1067-1071. (Pubitemid 351179338)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.3
, pp. 1067-1071
-
-
Paquin, I.1
Raeppel, S.2
Leit, S.3
Gaudette, F.4
Zhou, N.5
Moradei, O.6
Saavedra, O.7
Bernstein, N.8
Raeppel, F.9
Bouchain, G.10
Frechette, S.11
Woo, S.H.12
Vaisburg, A.13
Fournel, M.14
Kalita, A.15
Robert, M.-F.16
Lu, A.17
Trachy-Bourget, M.-C.18
Yan, P.T.19
Liu, J.20
Rahil, J.21
MacLeod, A.R.22
Besterman, J.M.23
Li, Z.24
Delorme, D.25
more..
-
13
-
-
55549093722
-
2- Trifluoroacetylthiophene oxadiazoles as potent and selective class II human histone deacetylase inhibitors
-
Ester, M.; Sergio, A.; Danila, B.; Ottavia, C.; Federica, F.; Maria, V.O.; Maria, C.P.; Michael, R.; Rita, S.; Christian, S.; Philip, J. 2- Trifluoroacetylthiophene oxadiazoles as potent and selective class II human histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 6083-6087.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 6083-6087
-
-
Ester, M.1
Sergio, A.2
Danila, B.3
Ottavia, C.4
Federica, F.5
Maria, V.O.6
Maria, C.P.7
Michael, R.8
Rita, S.9
Christian, S.10
Philip, J.11
-
14
-
-
34547592204
-
Design synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors
-
Shoukou, L.; Chihiro, S.; Kiyoshi, O.; Motomu, S.; Satoko, M.; Mayumi, S.; Minoru, Y.; Yuichi, H.; Hiroyuki, M. Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 4895-4900.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 4895-4900
-
-
Shoukou, L.1
Chihiro, S.2
Kiyoshi, O.3
Motomu, S.4
Satoko, M.5
Mayumi, S.6
Minoru, Y.7
Yuichi, H.8
Hiroyuki, M.9
-
15
-
-
27744496468
-
Non-hydroxamate histone deacetylase inhibitors
-
DOI 10.2174/092986705774454706
-
Suzuki, T.; Miyata, N. Non-hydroxamate histone deacetylase inhibitors. Curr. Med. Chem., 2005, 12(24), 2867-2880. (Pubitemid 41601562)
-
(2005)
Current Medicinal Chemistry
, vol.12
, Issue.24
, pp. 2867-2880
-
-
Suzuki, T.1
Miyata, N.2
-
16
-
-
33745164355
-
Substituted N-(2-aminophenyl)-benzamides, (E)-N-(2-aminophenyl)- acrylamides and their analogues: Novel classes of histone deacetylase inhibitors
-
DOI 10.1016/j.bmcl.2006.05.005, PII S0960894X06005312
-
Moradei, O.; Leit, S.; Zhou, N.; Frechette, S.; Paquin, I.; Raeppel, S.; Gaudette, F.; Bouchain, G.; Woo, S.H.; Vaisburg, A.; Fournel, M.; Kalita, A.; Lu, A.; Trachy- Bourget, M.-C.; Yan, P.T.; Liu, J.; Li, Z.; Rahil, J.; MacLeod, A.R.; Besterman, J.M.; Delorme, D. Substituted N-(2-aminophenyl)-benzamides, (E)-N-(2-aminophenyl)- acrylamides and their analogues: Novel classes of histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2006, 16, 4048-4052. (Pubitemid 43903209)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.15
, pp. 4048-4052
-
-
Moradei, O.1
Leit, S.2
Zhou, N.3
Frechette, S.4
Paquin, I.5
Raeppel, S.6
Gaudette, F.7
Bouchain, G.8
Woo, S.H.9
Vaisburg, A.10
Fournel, M.11
Kalita, A.12
Lu, A.13
Trachy-Bourget, M.-C.14
Yan, P.T.15
Liu, J.16
Li, Z.17
Rahil, J.18
MacLeod, A.R.19
Besterman, J.M.20
Delorme, D.21
more..
-
17
-
-
38949215072
-
4-(Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitors
-
DOI 10.1016/j.bmcl.2007.12.057, PII S0960894X07015168
-
Frechette, S.; Leit, S.; Hyung, S.; Lapointe, G.; Jeannotte, G.; Moradei, O.; Paquin, I.; Raeppel, S.; Leit, S.; Gaudette, F.; Zhou, N.; Moradei, O.; Saavedra, O.; Bernstein, N.; Raeppel, F.; Bouchain, G.; Frechette, S.; Woo, S.; Vaisburg, A.; Fournel, M.; Kalita, A.; Robert, M.; Lu, A.; Claude, M.; Bourget, T.; Yan, T.; Liu, J.; Rahil, A.; MacLeod, R.; Besterman, J.L.; Delorme, Z. 4- (Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 1502-1506. (Pubitemid 351226519)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.4
, pp. 1502-1506
-
-
Frechette, S.1
Leit, S.2
Woo, S.H.3
Lapointe, G.4
Jeannotte, G.5
Moradei, O.6
Paquin, I.7
Bouchain, G.8
Raeppel, S.9
Gaudette, F.10
Zhou, N.11
Vaisburg, A.12
Fournel, M.13
Yan, P.T.14
Trachy-Bourget, M.-C.15
Kalita, A.16
Robert, M.-F.17
Lu, A.18
Rahil, J.19
Robert MacLeod, A.20
Besterman, J.M.21
Li, Z.22
Delorme, D.23
more..
-
18
-
-
78650226214
-
Rationalization of physicochemical properties of alkanoic acid derivatives towards histone deacetylase inhibition
-
Jaiswal, D.; Karthikeyan, C.; Trivedi, P. Rationalization of physicochemical properties of alkanoic acid derivatives towards histone deacetylase inhibition. Internet Electron. J. Mol. Des., 2006, 5, 13-26.
-
(2006)
Internet Electron. J. Mol. Des.
, vol.5
, pp. 13-26
-
-
Jaiswal, D.1
Karthikeyan, C.2
Trivedi, P.3
-
19
-
-
34249909975
-
QSAR modeling of sulfonamide inhibitors of histone deacetylase
-
Jaiswal, D.; Karthikeyan, C.; Shrivastava, S.K.; Trivedi, P. QSAR modeling of sulfonamide inhibitors of histone deacetylase. Internet Electron. J. Mol. Des., 2006, 5, 345-54.
-
(2006)
Internet Electron. J. Mol. Des.
, vol.5
, pp. 345-54
-
-
Jaiswal, D.1
Karthikeyan, C.2
Shrivastava, S.K.3
Trivedi, P.4
-
20
-
-
43749108844
-
SAR and QSAR study on 2- aminothiazole derivatives, modulators of transcriptional repression in Huntington's disease
-
Samantha, L.; Cesare, M.; Aleksey, K.; Mattia, S.; Stefano, M.; Elena, C.; Dorotea, R.; Alessandro, C. SAR and QSAR study on 2- aminothiazole derivatives, modulators of transcriptional repression in Huntington's disease. Bioorg. Med. Chem. Lett. 2008, 16, 5695-5703.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 5695-5703
-
-
Samantha, L.1
Cesare, M.2
Aleksey, K.3
Mattia, S.4
Stefano, M.5
Elena, C.6
Dorotea, R.7
Alessandro, C.8
-
21
-
-
78650227201
-
-
User manual Phase, version 3.0, Schrödinger, LLC, New York, NY
-
User manual Phase, version 3.0, Schrödinger, LLC, New York, NY, 2008.
-
(2008)
-
-
-
22
-
-
33845868822
-
PHASE: A new engine for pharmacophore perception, 3D QSAR model development, and 3D database screening: 1. Methodology and preliminary results
-
DOI 10.1007/s10822-006-9087-6
-
Dixon, S.L.; Smondyrev, A.M.; Knoll, E.H.; Rao, S.N.; Shaw, D.E.; Friesner, R.A. PHASE: A new engine for pharmacophore perception, 3D QSAR model development, and 3D database screening: 1. Methodology and preliminary results. J. Comput. Aided Mol. Des., 2006, 20, 647-671. (Pubitemid 46023928)
-
(2006)
Journal of Computer-Aided Molecular Design
, vol.20
, Issue.10-11
, pp. 647-671
-
-
Dixon, S.L.1
Smondyrev, A.M.2
Knoll, E.H.3
Rao, S.N.4
Shaw, D.E.5
Friesner, R.A.6
-
23
-
-
78650177876
-
Pharmacophore generation and atom-based 3D-QSAR of novel 2-(4- methylsulfonylphenyl)pyrimidines as COX-2 inhibitors
-
DOI 10.1007/s11030-009-9183-3
-
Shah, U.A.; Deokar, H.S.; Kadam, S.S.; Kulkarni, V.M. Pharmacophore generation and atom-based 3D-QSAR of novel 2-(4- methylsulfonylphenyl) pyrimidines as COX-2 inhibitors. Mol. Divers., 2010. DOI 10.1007/s11030-009- 9183-3.
-
Mol. Divers.
, vol.2010
-
-
Shah, U.A.1
Deokar, H.S.2
Kadam, S.S.3
Kulkarni, V.M.4
|