-
1
-
-
34247512663
-
-
World Cancer Report 2014, World Health Organization, Geneva
-
Internaional Agency for Research on Cancer, World Cancer Report 2014, World Health Organization, Geneva, 2014.
-
(2014)
Internaional Agency for Research on Cancer
-
-
-
2
-
-
84871602057
-
Challenges in the design of multitarget drugs against multifactorial pathologies: A new life for medicinal chemistry?
-
L. Costantino, D. Barlocco, Challenges in the design of multitarget drugs against multifactorial pathologies: a new life for medicinal chemistry? Future Med. Chem. 5 (2013) 5-7.
-
(2013)
Future Med. Chem.
, vol.5
, pp. 5-7
-
-
Costantino, L.1
Barlocco, D.2
-
3
-
-
0242610850
-
Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA
-
M.S. Kim, M. Blake, J.H. Baek, G. Kohlhagen, Y. Pommier, F. Carrier, Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA, Cancer Res. 63 (2003) 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
-
4
-
-
70949083604
-
Synergistic antitumor effect between vorinostat and topotecan in small cell lung cancer cells is mediated by generation of reactive oxygen species and DNA damage-induced apoptosis
-
F. Bruzzese, M. Rocco, S. Castelli, E. Di Gennaro, A. Desideri, A. Budillon, Synergistic antitumor effect between vorinostat and topotecan in small cell lung cancer cells is mediated by generation of reactive oxygen species and DNA damage-induced apoptosis, Mol. Cancer Ther. 8 (2009) 3075-3087.
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 3075-3087
-
-
Bruzzese, F.1
Rocco, M.2
Castelli, S.3
Di Gennaro, E.4
Desideri, A.5
Budillon, A.6
-
5
-
-
23044487814
-
It's about time: Scheduling alters effect of histone deacetylase inhibitors on camptothecin-treated cells
-
R.L. Bevins, S.G. Zimmer, It's about time: scheduling alters effect of histone deacetylase inhibitors on camptothecin-treated cells, Cancer Res. 65 (2005) 6957-6966.
-
(2005)
Cancer Res.
, vol.65
, pp. 6957-6966
-
-
Bevins, R.L.1
Zimmer, S.G.2
-
6
-
-
18744408483
-
The histone-deacetylase inhibitor SAHA potentiates proapoptotic effects of 5-fluorouracil and irinotecan in hepatoma cells
-
M. Ocker, A. Alajati, M. Ganslmayer, S. Zopf, M. Luders, D. Neureiter, E.G. Hahn, D. Schuppan, C. Herold, The histone-deacetylase inhibitor SAHA potentiates proapoptotic effects of 5-fluorouracil and irinotecan in hepatoma cells, J. Cancer Res. Clin. Oncol. 131 (2005) 385-394.
-
(2005)
J. Cancer Res. Clin. Oncol.
, vol.131
, pp. 385-394
-
-
Ocker, M.1
Alajati, A.2
Ganslmayer, M.3
Zopf, S.4
Luders, M.5
Neureiter, D.6
Hahn, E.G.7
Schuppan, D.8
Herold, C.9
-
7
-
-
77956059770
-
Vorinostat enhances the cytotoxic effects of the topoisomerase i inhibitor SN38 in glioblastoma cell lines
-
B. Sarcar, S. Kahali, P. Chinnaiyan, Vorinostat enhances the cytotoxic effects of the topoisomerase I inhibitor SN38 in glioblastoma cell lines, J. Neuro-Oncol. 99 (2010) 201-207.
-
(2010)
J. Neuro-Oncol.
, vol.99
, pp. 201-207
-
-
Sarcar, B.1
Kahali, S.2
Chinnaiyan, P.3
-
8
-
-
36048958965
-
Histone deacetylase inhibitors: Overview and perspectives
-
M. Dokmanovic, C. Clarke, P.A. Marks, Histone deacetylase inhibitors: overview and perspectives, Mol. Cancer Res. 5 (2007) 981-989.
-
(2007)
Mol. Cancer Res.
, vol.5
, pp. 981-989
-
-
Dokmanovic, M.1
Clarke, C.2
Marks, P.A.3
-
9
-
-
33745320974
-
Targeting histone deacetylase in cancer therapy
-
H.Y. Lin, C.S. Chen, S.P. Lin, J.R. Weng, C.S. Chen, Targeting histone deacetylase in cancer therapy, Med. Res. Rev. 26 (2006) 397-413.
-
(2006)
Med. Res. Rev.
, vol.26
, pp. 397-413
-
-
Lin, H.Y.1
Chen, C.S.2
Lin, S.P.3
Weng, J.R.4
Chen, C.S.5
-
10
-
-
55749101363
-
Histone deacetylase inhibitors in cancer therapy
-
M.J. Lee, Y.S. Kim, S. Kummar, G. Giaccone, J.B. Trepel, Histone deacetylase inhibitors in cancer therapy, Curr. Opin. Oncol. 20 (2008) 639-649.
-
(2008)
Curr. Opin. Oncol.
, vol.20
, pp. 639-649
-
-
Lee, M.J.1
Kim, Y.S.2
Kummar, S.3
Giaccone, G.4
Trepel, J.B.5
-
11
-
-
33644663872
-
Histone acetylationindependent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes
-
C.S. Chen, S.C. Weng, P.H. Tseng, H.P. Lin, C.S. Chen, Histone acetylationindependent effect of histone deacetylase inhibitors on Akt through the reshuffling of protein phosphatase 1 complexes, J. Biol. Chem. 280 (2005) 38879-38887.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 38879-38887
-
-
Chen, C.S.1
Weng, S.C.2
Tseng, P.H.3
Lin, H.P.4
Chen, C.S.5
-
12
-
-
84897386255
-
Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
-
K. Nepali, S. Sharma, M. Sharma, P. Bedi, K. Dhar, Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids, Eur. J. Med. Chem. 77 (2014) 422-487.
-
(2014)
Eur. J. Med. Chem.
, vol.77
, pp. 422-487
-
-
Nepali, K.1
Sharma, S.2
Sharma, M.3
Bedi, P.4
Dhar, K.5
-
13
-
-
84897447871
-
Histone deacetylases inhibitors: Conjugation to other anti-tumour pharmacophores provides novel tools for cancer treatment
-
K.A. Papavassiliou, A.G. Papavassiliou, Histone deacetylases inhibitors: conjugation to other anti-tumour pharmacophores provides novel tools for cancer treatment, Expert Opin. Invest. Drugs (2013) 1-4.
-
(2013)
Expert Opin. Invest. Drugs
, pp. 1-4
-
-
Papavassiliou, K.A.1
Papavassiliou, A.G.2
-
14
-
-
71449109387
-
New patented histone deacetylase inhibitors
-
H. Wang, B.W. Dymock, New patented histone deacetylase inhibitors, Expert Opin. Ther. Pat. 19 (2009) 1727-1757.
-
(2009)
Expert Opin. Ther. Pat.
, vol.19
, pp. 1727-1757
-
-
Wang, H.1
Dymock, B.W.2
-
15
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27- 275, with marked in vivo antitumor activity against human tumors
-
A. Saito, T. Yamashita, Y. Mariko, Y. Nosaka, K. Tsuchiya, T. Ando, T. Suzuki, T. Tsuruo, O. Nakanishi, A synthetic inhibitor of histone deacetylase, MS-27- 275, with marked in vivo antitumor activity against human tumors, Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 4592-4597.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Mariko, Y.3
Nosaka, Y.4
Tsuchiya, K.5
Ando, T.6
Suzuki, T.7
Tsuruo, T.8
Nakanishi, O.9
-
16
-
-
0033199896
-
Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma
-
R.D. Glick, S.L. Swendeman, D.C. Coffey, R.A. Rifkind, P.A. Marks, V.M. Richon, M.P. La Quaglia, Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma, Cancer Res. 59 (1999) 4392-4399.
-
(1999)
Cancer Res.
, vol.59
, pp. 4392-4399
-
-
Glick, R.D.1
Swendeman, S.L.2
Coffey, D.C.3
Rifkind, R.A.4
Marks, P.A.5
Richon, V.M.6
La Quaglia, M.P.7
-
17
-
-
0034665124
-
Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
-
L.M. Butler, D.B. Agus, H.I. Scher, B. Higgins, A. Rose, C. Cordon-Cardo, H.T. Thaler, R.A. Rifkind, P.A. Marks, V.M. Richon, Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo, Cancer Res. 60 (2000) 5165-5170.
-
(2000)
Cancer Res.
, vol.60
, pp. 5165-5170
-
-
Butler, L.M.1
Agus, D.B.2
Scher, H.I.3
Higgins, B.4
Rose, A.5
Cordon-Cardo, C.6
Thaler, H.T.7
Rifkind, R.A.8
Marks, P.A.9
Richon, V.M.10
-
18
-
-
60549102514
-
Non-peptide macrocyclic histone deacetylase inhibitors
-
A.K. Oyelere, P.C. Chen, W. Guerrant, S.C. Mwakwari, R. Hood, Y. Zhang, Y. Fan, Non-peptide macrocyclic histone deacetylase inhibitors, J. Med. Chem. 52 (2009) 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
-
19
-
-
77949353758
-
Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-Nhydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
-
X. Cai, H.X. Zhai, J. Wang, J. Forrester, H. Qu, L. Yin, C.J. Lai, R. Bao, C. Qian, Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-Nhydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer, J. Med. Chem. 53 (2010) 2000-2009.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 2000-2009
-
-
Cai, X.1
Zhai, H.X.2
Wang, J.3
Forrester, J.4
Qu, H.5
Yin, L.6
Lai, C.J.7
Bao, R.8
Qian, C.9
-
20
-
-
77951708371
-
CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity
-
C.J. Lai, R. Bao, X. Tao, J. Wang, R. Atoyan, H. Qu, D.G. Wang, L. Yin, M. Samson, J. Forrester, B. Zifcak, G.X. Xu, S. DellaRocca, H.X. Zhai, X. Cai, W.E. Munger, M. Keegan, C.V. Pepicelli, C. Qian, 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. 70 (2010) 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
-
21
-
-
65249135408
-
Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: A series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rbeta, and histone deacetylases
-
S. Mahboobi, S. Dove, A. Sellmer, M. Winkler, E. Eichhorn, H. Pongratz, T. Ciossek, T. Baer, T. Maier, T. Beckers, Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: a series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rbeta, and histone deacetylases, J. Med. Chem. 52 (2009) 2265-2279.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2265-2279
-
-
Mahboobi, S.1
Dove, S.2
Sellmer, A.3
Winkler, M.4
Eichhorn, E.5
Pongratz, H.6
Ciossek, T.7
Baer, T.8
Maier, T.9
Beckers, T.10
-
22
-
-
78650321835
-
Novel chimeric histone deacetylase inhibitors: A series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR) human epidermal growth factor receptor 2 (HER2) and histone deacetylase activity
-
S. Mahboobi, A. Sellmer, M. Winkler, E. Eichhorn, H. Pongratz, T. Ciossek, T. Baer, T. Maier, T. Beckers, Novel chimeric histone deacetylase inhibitors: a series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity, J. Med. Chem. 53 (2010) 8546-8555.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8546-8555
-
-
Mahboobi, S.1
Sellmer, A.2
Winkler, M.3
Eichhorn, E.4
Pongratz, H.5
Ciossek, T.6
Baer, T.7
Maier, T.8
Beckers, T.9
-
23
-
-
84877834926
-
Current trends in the development of histone deacetylase inhibitors: A review of recent patent applications
-
F. Thaler, Current trends in the development of histone deacetylase inhibitors: a review of recent patent applications, Pharm. Pat. Anal. 1 (2012) 75-90.
-
(2012)
Pharm. Pat. Anal.
, vol.1
, pp. 75-90
-
-
Thaler, F.1
-
24
-
-
84879641705
-
The design and synthesis of a new class of RTK/HDAC dual-targeted inhibitors
-
X. Zhang, M. Su, Y. Chen, J. Li, W. Lu, The design and synthesis of a new class of RTK/HDAC dual-targeted inhibitors, Molecules 18 (2013) 6491-6503.
-
(2013)
Molecules
, vol.18
, pp. 6491-6503
-
-
Zhang, X.1
Su, M.2
Chen, Y.3
Li, J.4
Lu, W.5
-
25
-
-
84877794404
-
The discovery of colchicine-SAHA hybrids as a new class of antitumor agents
-
X. Zhang, J. Zhang, L.J. Tong, Y. Luo, M.B. Su, Y. Zang, J. Li, W. Lu, Y. Chen, The discovery of colchicine-SAHA hybrids as a new class of antitumor agents, Bioorg. Med. Chem. 21 (2013) 3240-3244.
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 3240-3244
-
-
Zhang, X.1
Zhang, J.2
Tong, L.J.3
Luo, Y.4
Su, M.B.5
Zang, Y.6
Li, J.7
Lu, W.8
Chen, Y.9
-
26
-
-
84885858940
-
The discovery and optimization of novel dual inhibitors of topoisomerase II and histone deacetylase
-
X. Zhang, B. Bao, X. Yu, L. Tong, Y. Luo, Q. Huang, M. Su, L. Sheng, J. Li, H. Zhu, B. Yang, X. Zhang, Y. Chen, W. Lu, The discovery and optimization of novel dual inhibitors of topoisomerase II and histone deacetylase, Bioorg. Med. Chem. 21 (2013) 6981-6995.
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 6981-6995
-
-
Zhang, X.1
Bao, B.2
Yu, X.3
Tong, L.4
Luo, Y.5
Huang, Q.6
Su, M.7
Sheng, L.8
Li, J.9
Zhu, H.10
Yang, B.11
Zhang, X.12
Chen, Y.13
Lu, W.14
-
27
-
-
36148950997
-
FDA approval summary: Vorinostat for treatment of advanced primary cutaneous T-cell lymphoma
-
B.S. Mann, J.R. Johnson, M.H. Cohen, R. Justice, R. Pazdur, FDA approval summary: vorinostat for treatment of advanced primary cutaneous T-cell lymphoma, Oncologist 12 (2007) 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
-
28
-
-
77954884940
-
Romidepsin: A new therapy for cutaneous T-cell lymphoma and a potential therapy for solid tumors
-
C. Grant, F. Rahman, R. Piekarz, C. Peer, R. Frye, R.W. Robey, E.R. Gardner, W.D. Figg, S.E. Bates, Romidepsin: a new therapy for cutaneous T-cell lymphoma and a potential therapy for solid tumors, Expert Rev. Anticancer Ther. 10 (2010) 997-1008.
-
(2010)
Expert Rev. Anticancer Ther.
, vol.10
, pp. 997-1008
-
-
Grant, C.1
Rahman, F.2
Piekarz, R.3
Peer, C.4
Frye, R.5
Robey, R.W.6
Gardner, E.R.7
Figg, W.D.8
Bates, S.E.9
-
29
-
-
77955646151
-
Macrocyclic histone deacetylase inhibitors
-
S.C. Mwakwari, V. Patil, W. Guerrant, A.K. Oyelere, Macrocyclic histone deacetylase inhibitors, Curr. Top. Med. Chem. 10 (2010) 1423-1440.
-
(2010)
Curr. Top. Med. Chem.
, vol.10
, pp. 1423-1440
-
-
Mwakwari, S.C.1
Patil, V.2
Guerrant, W.3
Oyelere, A.K.4
-
30
-
-
84928774345
-
Belinostat: First global approval
-
R.M. Poole, Belinostat: first global approval, Drugs 74 (2014) 1543-1554.
-
(2014)
Drugs
, vol.74
, pp. 1543-1554
-
-
Poole, R.M.1
-
31
-
-
41149089267
-
Histone deacetylase inhibitors: From bench to clinic
-
M. Paris, M. Porcelloni, M. Binaschi, D. Fattori, Histone deacetylase inhibitors: from bench to clinic, J. Med. Chem. 51 (2008) 1505-1529.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 1505-1529
-
-
Paris, M.1
Porcelloni, M.2
Binaschi, M.3
Fattori, D.4
-
32
-
-
84860371953
-
Epigenetic protein families: A new frontier for drug discovery
-
C.H. Arrowsmith, C. Bountra, P.V. Fish, K. Lee, M. Schapira, Epigenetic protein families: a new frontier for drug discovery, Nat. Rev. Drug Discovery 11 (2012) 384-400.
-
(2012)
Nat. Rev. Drug Discovery
, vol.11
, pp. 384-400
-
-
Arrowsmith, C.H.1
Bountra, C.2
Fish, P.V.3
Lee, K.4
Schapira, M.5
-
33
-
-
84872594782
-
P53 acetylation enhances Taxol-induced apoptosis in human cancer cells
-
J.H. Kim, E.K. Yoon, H.J. Chung, S.Y. Park, K.M. Hong, C.H. Lee, Y.S. Lee, K. Choi, Y. Yang, K. Kim, I.H. Kim, p53 acetylation enhances Taxol-induced apoptosis in human cancer cells, Apoptosis 18 (2013) 110-120.
-
(2013)
Apoptosis
, vol.18
, pp. 110-120
-
-
Kim, J.H.1
Yoon, E.K.2
Chung, H.J.3
Park, S.Y.4
Hong, K.M.5
Lee, C.H.6
Lee, Y.S.7
Choi, K.8
Yang, Y.9
Kim, K.10
Kim, I.H.11
-
34
-
-
2442554084
-
Histone deacetylase inhibitors enhance paclitaxel-induced cell death in ovarian cancer cell lines independent of p53 status
-
N.H. Chobanian, V.L. Greenberg, J.M. Gass, C.P. Desimone, J.R. Van Nagell, S.G. Zimmer, Histone deacetylase inhibitors enhance paclitaxel-induced cell death in ovarian cancer cell lines independent of p53 status, Anticancer Res. 24 (2004) 539-545.
-
(2004)
Anticancer Res.
, vol.24
, pp. 539-545
-
-
Chobanian, N.H.1
Greenberg, V.L.2
Gass, J.M.3
Desimone, C.P.4
Van Nagell, J.R.5
Zimmer, S.G.6
-
35
-
-
83355172959
-
Synergistic antitumor effects of novel HDAC inhibitors and paclitaxel in vitro and in vivo
-
V. Zuco, M. De Cesare, R. Cincinelli, R. Nannei, C. Pisano, N. Zaffaroni, F. Zunino, Synergistic antitumor effects of novel HDAC inhibitors and paclitaxel in vitro and in vivo, PloS One 6 (2011) -29085.
-
(2011)
PloS One
, vol.6
, pp. 29085
-
-
Zuco, V.1
De Cesare, M.2
Cincinelli, R.3
Nannei, R.4
Pisano, C.5
Zaffaroni, N.6
Zunino, F.7
-
36
-
-
10844268815
-
Synthesis and characterization of a cobalamin-colchicine conjugate as a novel tumor-targeted cytotoxin
-
J.D. Bagnato, A.L. Eilers, R.A. Horton, C.B. Grissom, Synthesis and characterization of a cobalamin-colchicine conjugate as a novel tumor-targeted cytotoxin, J. Org. Chem. 69 (2004) 8987-8996.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 8987-8996
-
-
Bagnato, J.D.1
Eilers, A.L.2
Horton, R.A.3
Grissom, C.B.4
-
37
-
-
84871643254
-
Synthesis and biological evaluation of colchicine B-ring analogues tethered with halogenated benzyl moieties
-
L. Cosentino, M. Redondo-Horcajo, Y. Zhao, A.R. Santos, K.F. Chowdury, V. Vinader, Q.M. Abdallah, H. Abdel-Rahman, J.r.m. Fournier-Dit-Chabert, S.D. Shnyder, Synthesis and biological evaluation of colchicine B-ring analogues tethered with halogenated benzyl moieties, J. Med. Chem. 55 (2012) 11062-11066.
-
(2012)
J. Med. Chem.
, vol.55
, pp. 11062-11066
-
-
Cosentino, L.1
Redondo-Horcajo, M.2
Zhao, Y.3
Santos, A.R.4
Chowdury, K.F.5
Vinader, V.6
Abdallah, Q.M.7
Abdel-Rahman, H.8
Fournier-Dit-Chabert, J.R.M.9
Shnyder, S.D.10
-
38
-
-
36148950575
-
Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity
-
O.M. Moradei, T.C. Mallais, S. Frechette, I. Paquin, P.E. Tessier, S.M. Leit, M. Fournel, C. Bonfils, M.C. Trachy-Bourget, J.H. Liu, T.P. Yan, A.H. Lu, J. Rahil, J. Wang, S. Lefebvre, Z.M. Li, A.F. Vaisburg, J.M. Besterinan, Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity, J. Med. Chem. 50 (2007) 5543-5546.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 5543-5546
-
-
Moradei, O.M.1
Mallais, T.C.2
Frechette, S.3
Paquin, I.4
Tessier, P.E.5
Leit, S.M.6
Fournel, M.7
Bonfils, C.8
Trachy-Bourget, M.C.9
Liu, J.H.10
Yan, T.P.11
Lu, A.H.12
Rahil, J.13
Wang, J.14
Lefebvre, S.15
Li, Z.M.16
Vaisburg, A.F.17
Besterinan, J.M.18
-
39
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
M.A. Jordan, L. Wilson, Microtubules as a target for anticancer drugs, Nat. Rev. Cancer 4 (2004) 253-265.
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
|