-
1
-
-
84889262928
-
Polypharmacology: Foe or friend?
-
Peters, J. U. Polypharmacology: foe or friend? J. Med. Chem. 2013, 56, 8955-8971
-
(2013)
J. Med. Chem.
, vol.56
, pp. 8955-8971
-
-
Peters, J.U.1
-
2
-
-
84907943686
-
Polypharmacology: Challenges and opportunities in drug discovery
-
Anighoro, A.; Bajorath, J.; Rastelli, G. Polypharmacology: challenges and opportunities in drug discovery J. Med. Chem. 2014, 57, 7874-7887
-
(2014)
J. Med. Chem.
, vol.57
, pp. 7874-7887
-
-
Anighoro, A.1
Bajorath, J.2
Rastelli, G.3
-
3
-
-
54249155522
-
Network pharmacology: The next paradigm in drug discovery
-
Hopkins, A. L. Network pharmacology: the next paradigm in drug discovery Nat. Chem. Biol. 2008, 4, 682-690
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 682-690
-
-
Hopkins, A.L.1
-
4
-
-
69549109944
-
Conciliating binding efficiency and polypharmacology
-
Mestres, J.; Gregori-Puigjane, E. Conciliating binding efficiency and polypharmacology Trends Pharmacol. Sci. 2009, 30, 470-474
-
(2009)
Trends Pharmacol. Sci.
, vol.30
, pp. 470-474
-
-
Mestres, J.1
Gregori-Puigjane, E.2
-
5
-
-
77954052283
-
Systems approaches to polypharmacology and drug discovery
-
Boran, A. D.; Iyengar, R. Systems approaches to polypharmacology and drug discovery Curr. Opin. Drug. Discovery Dev. 2010, 13, 297-309
-
(2010)
Curr. Opin. Drug. Discovery Dev.
, vol.13
, pp. 297-309
-
-
Boran, A.D.1
Iyengar, R.2
-
6
-
-
33847065486
-
The epigenomics of cancer
-
Jones, P. A.; Baylin, S. B. The epigenomics of cancer Cell 2007, 128, 683-692
-
(2007)
Cell
, vol.128
, pp. 683-692
-
-
Jones, P.A.1
Baylin, S.B.2
-
7
-
-
33847076849
-
Chromatin modifications and their function
-
Kouzarides, T. Chromatin modifications and their function Cell 2007, 128, 693-705
-
(2007)
Cell
, vol.128
, pp. 693-705
-
-
Kouzarides, T.1
-
8
-
-
84894069675
-
Histone deacetylases inhibitors: Conjugation to other anti-tumour pharmacophores provides novel tools for cancer treatment
-
Papavassiliou, K. A.; Papavassiliou, A. G. Histone deacetylases inhibitors: conjugation to other anti-tumour pharmacophores provides novel tools for cancer treatment Expert. Opin. Invest. Drugs. 2014, 23, 291-294
-
(2014)
Expert. Opin. Invest. Drugs.
, vol.23
, pp. 291-294
-
-
Papavassiliou, K.A.1
Papavassiliou, A.G.2
-
9
-
-
79952158522
-
Rational therapeutic combinations with histone deacetylase inhibitors for the treatment of cancer
-
Thurn, K. T.; Thomas, S.; Moore, A.; Munster, P. N. Rational therapeutic combinations with histone deacetylase inhibitors for the treatment of cancer Future Oncol. 2011, 7, 263-283
-
(2011)
Future Oncol.
, vol.7
, pp. 263-283
-
-
Thurn, K.T.1
Thomas, S.2
Moore, A.3
Munster, P.N.4
-
10
-
-
36148950997
-
FDA approval summary: Vorinostat for treatment of advanced primary cutaneous T-cell lymphoma
-
Mann, B. S.; Johnson, J. R.; Cohen, M. H.; Justice, R.; Pazdur, R. FDA approval summary: vorinostat for treatment of advanced primary cutaneous T-cell lymphoma Oncologist 2007, 12, 1247-1252
-
(2007)
Oncologist
, vol.12
, pp. 1247-1252
-
-
Mann, B.S.1
Johnson, J.R.2
Cohen, M.H.3
Justice, R.4
Pazdur, R.5
-
11
-
-
84874410182
-
Histone deacetylase inhibitors (HDACIs): Multitargeted anticancer agents
-
Ververis, K.; Hiong, A.; Karagiannis, T. C.; Licciardi, P. V. Histone deacetylase inhibitors (HDACIs): multitargeted anticancer agents Biologics 2013, 7, 47-60
-
(2013)
Biologics
, vol.7
, pp. 47-60
-
-
Ververis, K.1
Hiong, A.2
Karagiannis, T.C.3
Licciardi, P.V.4
-
12
-
-
84877794404
-
The discovery of colchicine-SAHA hybrids as a new class of antitumor agents
-
Zhang, X.; Zhang, J.; Tong, L.; Luo, Y.; Su, M.; Zang, Y.; Li, J.; Lu, W.; Chen, Y. The discovery of colchicine-SAHA hybrids as a new class of antitumor agents Bioorg. Med. Chem. 2013, 21, 3240-3244
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 3240-3244
-
-
Zhang, X.1
Zhang, J.2
Tong, L.3
Luo, Y.4
Su, M.5
Zang, Y.6
Li, J.7
Lu, W.8
Chen, Y.9
-
13
-
-
21144444486
-
HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor
-
Kovacs, J. J.; Murphy, P. J.; Gaillard, S.; Zhao, X.; Wu, J. T.; Nicchitta, C. V.; Yoshida, M.; Toft, D. O.; Pratt, W. B.; Yao, T. P. HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor Mol. Cell 2005, 18, 601-607
-
(2005)
Mol. Cell
, vol.18
, pp. 601-607
-
-
Kovacs, J.J.1
Murphy, P.J.2
Gaillard, S.3
Zhao, X.4
Wu, J.T.5
Nicchitta, C.V.6
Yoshida, M.7
Toft, D.O.8
Pratt, W.B.9
Yao, T.P.10
-
14
-
-
77951708371
-
CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity
-
Lai, C. J.; Bao, R.; Tao, X.; Wang, J.; Atoyan, R.; Qu, H.; Wang, D. G.; Yin, L.; Samson, M.; Forrester, J.; Zifcak, B.; Xu, G. X.; DellaRocca, S.; Zhai, H. X.; Cai, X.; Munger, W. E.; Keegan, M.; Pepicelli, C. V.; Qian, C. CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity Cancer. Res. 2010, 70, 3647-3656
-
(2010)
Cancer. Res.
, vol.70
, pp. 3647-3656
-
-
Lai, C.J.1
Bao, R.2
Tao, X.3
Wang, J.4
Atoyan, R.5
Qu, H.6
Wang, D.G.7
Yin, L.8
Samson, M.9
Forrester, J.10
Zifcak, B.11
Xu, G.X.12
Dellarocca, S.13
Zhai, H.X.14
Cai, X.15
Munger, W.E.16
Keegan, M.17
Pepicelli, C.V.18
Qian, C.19
-
15
-
-
0242610850
-
Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA
-
Kim, M. S.; Blake, M.; Baek, J. H.; Kohlhagen, G.; Pommier, Y.; Carrier, F. Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA Cancer. Res. 2003, 63, 7291-7300
-
(2003)
Cancer. Res.
, vol.63
, pp. 7291-7300
-
-
Kim, M.S.1
Blake, M.2
Baek, J.H.3
Kohlhagen, G.4
Pommier, Y.5
Carrier, F.6
-
16
-
-
33751505528
-
Valproic acid, a histone deacetylase inhibitor, enhances sensitivity to doxorubicin in anaplastic thyroid cancer cells
-
Catalano, M. G.; Fortunati, N.; Pugliese, M.; Poli, R.; Bosco, O.; Mastrocola, R.; Aragno, M.; Boccuzzi, G. Valproic acid, a histone deacetylase inhibitor, enhances sensitivity to doxorubicin in anaplastic thyroid cancer cells J. Endocrinol. 2006, 191, 465-472
-
(2006)
J. Endocrinol.
, vol.191
, pp. 465-472
-
-
Catalano, M.G.1
Fortunati, N.2
Pugliese, M.3
Poli, R.4
Bosco, O.5
Mastrocola, R.6
Aragno, M.7
Boccuzzi, G.8
-
17
-
-
23044487814
-
Its about time: Scheduling alters effect of histone deacetylase inhibitors on camptothecin-treated cells
-
Bevins, R. L.; Zimmer, S. G. Its about time: scheduling alters effect of histone deacetylase inhibitors on camptothecin-treated cells Cancer. Res. 2005, 65, 6957-6966
-
(2005)
Cancer. Res.
, vol.65
, pp. 6957-6966
-
-
Bevins, R.L.1
Zimmer, S.G.2
-
18
-
-
84857406206
-
Dual targeting of histone deacetylase and topoisomerase II with novel bifunctional inhibitors
-
Guerrant, W.; Patil, V.; Canzoneri, J. C.; Oyelere, A. K. Dual targeting of histone deacetylase and topoisomerase II with novel bifunctional inhibitors J. Med. Chem. 2012, 55, 1465-1477
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1465-1477
-
-
Guerrant, W.1
Patil, V.2
Canzoneri, J.C.3
Oyelere, A.K.4
-
19
-
-
78650670619
-
Recent advances in the development of dual topoisomerase i and II inhibitors as anticancer drugs
-
Salerno, S.; Da Settimo, F.; Taliani, S.; Simorini, F.; La Motta, C.; Fornaciari, G.; Marini, A. M. Recent advances in the development of dual topoisomerase I and II inhibitors as anticancer drugs Curr. Med. Chem. 2010, 17, 4270-4290
-
(2010)
Curr. Med. Chem.
, vol.17
, pp. 4270-4290
-
-
Salerno, S.1
Da Settimo, F.2
Taliani, S.3
Simorini, F.4
La Motta, C.5
Fornaciari, G.6
Marini, A.M.7
-
20
-
-
67249138744
-
Evodiamine: A novel anti-cancer alkaloid from Evodia rutaecarpa
-
Jiang, J.; Hu, C. Evodiamine: a novel anti-cancer alkaloid from Evodia rutaecarpa Molecules 2009, 14, 1852-1859
-
(2009)
Molecules
, vol.14
, pp. 1852-1859
-
-
Jiang, J.1
Hu, C.2
-
21
-
-
78149253942
-
Selection of evodiamine as a novel topoisomerase i inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents
-
Dong, G.; Sheng, C.; Wang, S.; Miao, Z.; Yao, J.; Zhang, W. Selection of evodiamine as a novel topoisomerase I inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents J. Med. Chem. 2010, 53, 7521-7531
-
(2010)
J. Med. Chem.
, vol.53
, pp. 7521-7531
-
-
Dong, G.1
Sheng, C.2
Wang, S.3
Miao, Z.4
Yao, J.5
Zhang, W.6
-
22
-
-
84866328968
-
New tricks for an old natural product: Discovery of highly potent evodiamine derivatives as novel antitumor agents by systemic structure-activity relationship analysis and biological evaluations
-
Dong, G.; Wang, S.; Miao, Z.; Yao, J.; Zhang, Y.; Guo, Z.; Zhang, W.; Sheng, C. New tricks for an old natural product: discovery of highly potent evodiamine derivatives as novel antitumor agents by systemic structure-activity relationship analysis and biological evaluations J. Med. Chem. 2012, 55, 7593-7613
-
(2012)
J. Med. Chem.
, vol.55
, pp. 7593-7613
-
-
Dong, G.1
Wang, S.2
Miao, Z.3
Yao, J.4
Zhang, Y.5
Guo, Z.6
Zhang, W.7
Sheng, C.8
-
23
-
-
84905661082
-
Design, synthesis and biological evaluation of E-ring modified evodiamine derivatives as novel antitumor agents
-
Fang, K.; Dong, G. Q.; Gong, H.; Liu, N.; Li, Z. G.; Zhu, S. P.; Miao, Z. Y.; Yao, J. Z.; Zhang, W. N.; Sheng, C. Q. Design, synthesis and biological evaluation of E-ring modified evodiamine derivatives as novel antitumor agents Chin. Chem. Lett. 2014, 25, 978-982
-
(2014)
Chin. Chem. Lett.
, vol.25
, pp. 978-982
-
-
Fang, K.1
Dong, G.Q.2
Gong, H.3
Liu, N.4
Li, Z.G.5
Zhu, S.P.6
Miao, Z.Y.7
Yao, J.Z.8
Zhang, W.N.9
Sheng, C.Q.10
-
24
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
Finnin, M. S.; Donigian, J. R.; Cohen, A.; Richon, V. M.; Rifkind, R. A.; Marks, P. A.; Breslow, R.; Pavletich, N. P. Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors Nature 1999, 401, 188-193
-
(1999)
Nature
, vol.401
, pp. 188-193
-
-
Finnin, M.S.1
Donigian, J.R.2
Cohen, A.3
Richon, V.M.4
Rifkind, R.A.5
Marks, P.A.6
Breslow, R.7
Pavletich, N.P.8
-
25
-
-
84858015797
-
Oxadiazoles in medicinal chemistry
-
Bostrom, J.; Hogner, A.; Llinas, A.; Wellner, E.; Plowright, A. T. Oxadiazoles in medicinal chemistry J. Med. Chem. 2012, 55, 1817-1830
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1817-1830
-
-
Bostrom, J.1
Hogner, A.2
Llinas, A.3
Wellner, E.4
Plowright, A.T.5
-
26
-
-
60549102514
-
Non-peptide macrocyclic histone deacetylase inhibitors
-
Oyelere, A. K.; Chen, P. C.; Guerrant, W.; Mwakwari, S. C.; Hood, R.; Zhang, Y.; Fan, Y. Non-peptide macrocyclic histone deacetylase inhibitors J. Med. Chem. 2009, 52, 456-468
-
(2009)
J. Med. Chem.
, vol.52
, pp. 456-468
-
-
Oyelere, A.K.1
Chen, P.C.2
Guerrant, W.3
Mwakwari, S.C.4
Hood, R.5
Zhang, Y.6
Fan, Y.7
-
27
-
-
77249087051
-
Chemical phylogenetics of histone deacetylases
-
Bradner, J. E.; West, N.; Grachan, M. L.; Greenberg, E. F.; Haggarty, S. J.; Warnow, T.; Mazitschek, R. Chemical phylogenetics of histone deacetylases Nat. Chem. Biol. 2010, 6, 238-243
-
(2010)
Nat. Chem. Biol.
, vol.6
, pp. 238-243
-
-
Bradner, J.E.1
West, N.2
Grachan, M.L.3
Greenberg, E.F.4
Haggarty, S.J.5
Warnow, T.6
Mazitschek, R.7
|