-
1
-
-
0015694748
-
A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining
-
Rowley, J.D. Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining. Nature, 1973, 243, 290-293.
-
(1973)
Nature
, vol.243
, pp. 290-293
-
-
Rowley J.D. Letter1
-
2
-
-
77951494873
-
Targeted cancer therapies in the twenty-first century: Lessons from imatinib
-
Stegmeier, F.; Warmuth, M.; Sellers, W.R.; Dorsch, M. Targeted cancer therapies in the twenty-first century: Lessons from imatinib. Clin. Pharmacol. Ther., 2010, 87, 543-552.
-
(2010)
Clin. Pharmacol. Ther.
, vol.87
, pp. 543-552
-
-
Stegmeier, F.1
Warmuth, M.2
Sellers, W.R.3
Dorsch, M.4
-
3
-
-
77950669895
-
New opportunities to treat the T315I-Bcr-Abl mutant in chronic myeloid leukaemia: Tyrosine kinase inhibitors and molecules that act by alternative mechanisms
-
Schenone, S.; Brullo, C.; Botta, M. New opportunities to treat the T315I-Bcr-Abl mutant in chronic myeloid leukaemia: Tyrosine kinase inhibitors and molecules that act by alternative mechanisms. Curr. Med. Chem., 2010, 17, 1220-1245.
-
(2010)
Curr. Med. Chem.
, vol.17
, pp. 1220-1245
-
-
Schenone, S.1
Brullo, C.2
Botta, M.3
-
4
-
-
61849163272
-
Molecular biology of bcr-abl1-positive chronic myeloid leukemia
-
Quintas-Cardama, A.; Cortes, J. Molecular biology of bcr-abl1-positive chronic myeloid leukemia. Blood, 2009, 113, 1619-1630.
-
(2009)
Blood
, vol.113
, pp. 1619-1630
-
-
Quintas-Cardama, A.1
Cortes, J.2
-
5
-
-
42149097162
-
Molecular basis explanation for imatinib resistance of BCR-ABL due to T315I and P-loop mutations from molecular dynamics simulations
-
DOI 10.1002/cncr.23355
-
Lee, T.S.; Potts, S.J.; Kantarjian, H.; Cortes, J.; Giles, F.; Albitar, M. Molecular basis explanation for imatinib resistance of BCR-ABL due to T315I and P-loop mutations from molecular dynamics simulations. Cancer, 2008, 112, 1744-1753. (Pubitemid 351536834)
-
(2008)
Cancer
, vol.112
, Issue.8
, pp. 1744-1753
-
-
Lee, T.-S.1
Potts, S.J.2
Kantarjian, H.3
Cortes, J.4
Giles, F.5
Albitar, M.6
-
6
-
-
79957958724
-
Recent developments in the third generation inhibitors of Bcr-Abl for overriding T315I mutation
-
Lu, X.Y.; Cai, Q.; Ding, K. Recent developments in the third generation inhibitors of Bcr-Abl for overriding T315I mutation. Curr. Med. Chem., 2011, 18, 2146-2157.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 2146-2157
-
-
Lu, X.Y.1
Cai, Q.2
Ding, K.3
-
7
-
-
34547660333
-
Targeted therapy and the T315I mutation in Philadelphia-positive leukemias
-
DOI 10.3324/haematol.11248
-
Soverini, S.; Iacobucci, I.; Baccarani, M.; Martinelli, G. Targeted therapy and the T315I mutation in Philadelphia-positive leukemias. Haematologica, 2007, 92, 437-439. (Pubitemid 350144288)
-
(2007)
Haematologica
, vol.92
, Issue.4
, pp. 437-439
-
-
Soverini, S.1
Iacobucci, I.2
Baccarani, M.3
Martinelli, G.4
-
8
-
-
52149123619
-
Core signaling pathways in human pancreatic cancers revealed by global genomic analyses
-
Jones, S.; Zhang, X.; Parsons, D.W.; Lin, J.C.; Leary, R.J.; Angenendt, P.; Mankoo, P.; Carter, H.; Kamiyama, H.; Jimeno, A.; Hong, S.M.; Fu, B.; Lin, M.T.; Calhoun, E.S.; Kamiyama, M.; Walter, K.; Nikolskaya, T.; Nikolsky, Y.; Hartigan, J.; Smith, D.R.; Hidalgo, M.; Leach, S.D.; Klein, A.P.; Jaffee, E.M.; Goggins, M.; Maitra, A.; Iacobuzio-Donahue, C.; Eshleman, J.R.; Kern, S.E.; Hruban, R.H.; Karchin, R.; Papadopoulos, N.; Parmigiani, G.; Vogelstein, B.; Velculescu, V.E.; Kinzler, K.W. Core signaling pathways in human pancreatic cancers revealed by global genomic analyses. Science, 2008, 321, 1801-1806.
-
(2008)
Science
, vol.321
, pp. 1801-1806
-
-
Jones, S.1
Zhang, X.2
Parsons, D.W.3
Lin, J.C.4
Leary, R.J.5
Angenendt, P.6
Mankoo, P.7
Carter, H.8
Kamiyama, H.9
Jimeno, A.10
Hong, S.M.11
Fu, B.12
Lin, M.T.13
Calhoun, E.S.14
Kamiyama, M.15
Walter, K.16
Nikolskaya, T.17
Nikolsky, Y.18
Hartigan, J.19
Smith, D.R.20
Hidalgo, M.21
Leach, S.D.22
Klein, A.P.23
Jaffee, E.M.24
Goggins, M.25
Maitra, A.26
Iacobuzio-Donahue, C.27
Eshleman, J.R.28
Kern, S.E.29
Hruban, R.H.30
Karchin, R.31
Papadopoulos, N.32
Parmigiani, G.33
Vogelstein, B.34
Velculescu, V.E.35
Kinzler, K.W.36
more..
-
9
-
-
10444280878
-
Strategies to overcome resistance to targeted protein kinase inhibitors
-
DOI 10.1038/nrd1579
-
Daub, H.; Specht, K.; Ullrich, A. Strategies to overcome resistance to targeted protein kinase inhibitors. Nat. Rev. Drug Discov., 2004, 3, 1001-1010. (Pubitemid 39642363)
-
(2004)
Nature Reviews Drug Discovery
, vol.3
, Issue.12
, pp. 1001-1010
-
-
Daub, H.1
Specht, K.2
Ullrich, A.3
-
10
-
-
70349100446
-
Histone deacetylase inhibitors: Current status and overview of recent clinical trials
-
Ma, X.; Ezzeldin, H.H.; Diasio, R.B. Histone deacetylase inhibitors: Current status and overview of recent clinical trials. Drugs, 2009, 69, 1911-1934.
-
(2009)
Drugs
, vol.69
, pp. 1911-1934
-
-
Ma, X.1
Ezzeldin, H.H.2
Diasio, R.B.3
-
11
-
-
67650090545
-
Histone deacetylase inhibitors: Potential in cancer therapy
-
Marks, P.A.; Xu, W.S. Histone deacetylase inhibitors: Potential in cancer therapy. J. Cell. Biochem., 2009, 107, 600-608.
-
(2009)
J. Cell. Biochem.
, vol.107
, pp. 600-608
-
-
Marks, P.A.1
Xu, W.S.2
-
12
-
-
61849144810
-
HDAC family: What are the cancer relevant targets?
-
Witt, O.; Deubzer, H.E.; Milde, T.; Oehme, I. HDAC family: What are the cancer relevant targets? Cancer Lett., 2009, 277, 8-21.
-
(2009)
Cancer Lett.
, vol.277
, pp. 8-21
-
-
Witt, O.1
Deubzer, H.E.2
Milde, T.3
Oehme, I.4
-
13
-
-
79955678223
-
Developing histone deacetylase inhibitors as anti-cancer therapeutics
-
Venugopal, B.; Evans, T.R. Developing histone deacetylase inhibitors as anti-cancer therapeutics. Curr. Med. Chem., 2011, 18, 1658-1671.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 1658-1671
-
-
Venugopal, B.1
Evans, T.R.2
-
14
-
-
0842277812
-
WAF1 involves changes in promoter-associated proteins, including HDAC1
-
DOI 10.1073/pnas.0307708100
-
Gui, C.Y.; Ngo, L.; Xu, W.S.; Richon, V.M.; Marks, P.A. Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1. Proc. Natl. Acad. Sci. U. S. A., 2004, 101, 1241-1246. (Pubitemid 38182673)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.5
, pp. 1241-1246
-
-
Gui, C.-Y.1
Ngo, L.2
Xu, W.S.3
Richon, V.M.4
Marks, P.A.5
-
15
-
-
0035048449
-
Histone deacetylases induce angiogenesis by negative regulation of tumor suppressor genes
-
DOI 10.1038/86507
-
Kim, M.S.; Kwon, H.J.; Lee, Y.M.; Baek, J.H.; Jang, J.E.; Lee, S.W.; Moon, E.J.; Kim, H.S.; Lee, S.K.; Chung, H.Y.; Kim, C.W.; Kim, K.W. Histone deacetylases induce angiogenesis by negative regulation of tumor suppressor genes. Nat. Med., 2001, 7, 437-443. (Pubitemid 32298546)
-
(2001)
Nature Medicine
, vol.7
, Issue.4
, pp. 437-443
-
-
Kim, M.S.1
Kwon, H.J.2
Lee, Y.M.3
Baek, J.H.4
Jang, J.-E.5
Lee, S.-W.6
Moon, E.-J.7
Kim, H.-S.8
Lee, S.-K.9
Chung, H.Y.10
Kim, C.W.11
Kim, K.-W.12
-
16
-
-
78649905409
-
Histone deacetylase inhibitors: A chemical genetics approach to understanding cellular functions
-
Marks, P.A. Histone deacetylase inhibitors: A chemical genetics approach to understanding cellular functions. Biochim. Biophys. Acta, 2010, 1799, 717-725.
-
(2010)
Biochim. Biophys. Acta
, vol.1799
, pp. 717-725
-
-
Marks, P.A.1
-
17
-
-
33748451151
-
Anticancer activities of histone deacetylase inhibitors
-
DOI 10.1038/nrd2133, PII NRD2133
-
Bolden, J.E.; Peart, M.J.; Johnstone, R.W. Anticancer activities of histone deacetylase inhibitors. Nat. Rev. Drug Disc., 2006, 5, 769-784. (Pubitemid 44348499)
-
(2006)
Nature Reviews Drug Discovery
, vol.5
, Issue.9
, pp. 769-784
-
-
Bolden, J.E.1
Peart, M.J.2
Johnstone, R.W.3
-
18
-
-
21144444486
-
HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor
-
DOI 10.1016/j.molcel.2005.04.021, PII S1097276505012840
-
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. (Pubitemid 40726236)
-
(2005)
Molecular Cell
, vol.18
, Issue.5
, pp. 601-607
-
-
Kovacs, J.J.1
Murphy, P.J.M.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
-
19
-
-
22844432021
-
Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: A novel basis for antileukemia activity of histone deacetylase inhibitors
-
DOI 10.1074/jbc.C500186200
-
Bali, P.; Pranpat, M.; Bradner, J.; Balasis, M.; Fiskus, W.; Guo, F.; Rocha, K.; Kumaraswamy, S.; Boyapalle, S.; Atadja, P.; Seto, E.; Bhalla, K. Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: A novel basis for antileukemia activity of histone deacetylase inhibitors. J. Biol. Chem., 2005, 280, 26729-26734. (Pubitemid 41040705)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.29
, pp. 26729-26734
-
-
Bali, P.1
Pranpat, M.2
Bradner, J.3
Balasis, M.4
Fiskus, W.5
Guo, F.6
Rocha, K.7
Kumaraswamy, S.8
Boyapalle, S.9
Atadja, P.10
Seto, E.11
Bhalla, K.12
-
20
-
-
67449145358
-
Rational combinations using HDAC inhibitors
-
Bots, M.; Johnstone, R.W. Rational combinations using HDAC inhibitors. Clin. Cancer Res., 2009, 15, 3970-3977.
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 3970-3977
-
-
Bots, M.1
Johnstone, R.W.2
-
21
-
-
77950860448
-
Inside HDAC with HDAC inhibitors
-
Bertrand, P. Inside HDAC with HDAC inhibitors. Eur. J. Med. Chem., 2010, 45, 2095-2116.
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 2095-2116
-
-
Bertrand, P.1
-
22
-
-
0242522928
-
Histone deacetylase inhibitors
-
DOI 10.1021/jm0303094
-
Miller, T.A.; Witter, D.J.; Belvedere, S. Histone deacetylase inhibitors. J. Med. Chem., 2003, 46, 5097-5116. (Pubitemid 37414179)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.24
, pp. 5097-5116
-
-
Miller, T.A.1
Witter, D.J.2
Belvedere, S.3
-
23
-
-
42049118549
-
Isoform-selective histone deacetylase inhibitors
-
DOI 10.2174/138161208783885335
-
Itoh, Y.; Suzuki, T.; Miyata, N. Isoform-selective histone deacetylase inhibitors. Curr. Pharm. Des., 2008, 14, 529-544. (Pubitemid 351516877)
-
(2008)
Current Pharmaceutical Design
, vol.14
, Issue.6
, pp. 529-544
-
-
Itoh, Y.1
Suzuki, T.2
Miyata, N.3
-
24
-
-
42049096372
-
Chemical origins of isoform selectivity in histone deacetylase inhibitors
-
DOI 10.2174/138161208783885353
-
Butler, K.V.; Kozikowski, A.P. Chemical origins of isoform selectivity in histone deacetylase inhibitors. Curr. Pharm. Des., 2008, 14, 505-528. (Pubitemid 351516876)
-
(2008)
Current Pharmaceutical Design
, vol.14
, Issue.6
, pp. 505-528
-
-
Butler, K.V.1
Kozikowski, A.P.2
-
25
-
-
71749084293
-
Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide
-
Canzoneri, J.C.; Chen, P.C.; Oyelere, A.K. Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide. Bioorg. Med. Chem. Lett., 2009, 19, 6588-6590.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6588-6590
-
-
Canzoneri, J.C.1
Chen, P.C.2
Oyelere, A.K.3
-
26
-
-
26444441453
-
Alkyl-substituted polyaminohydroxamic acids: A novel class of targeted histone deacetylase inhibitors
-
DOI 10.1021/jm0505009
-
Varghese, S.; Gupta, D.; Baran, T.; Jiemjit, A.; Gore, S.D.; Casero, R.A.; Woster, P.M. Alkyl-substituted polyaminohydroxamic acids: A novel class of targeted histone deacetylase inhibitors. J. Med. Chem., 2005, 48, 6350-6365. (Pubitemid 41428987)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.20
, pp. 6350-6365
-
-
Varghese, S.1
Gupta, D.2
Baran, T.3
Jiemjit, A.4
Gore, S.D.5
Casero Jr., R.A.6
Woster, P.M.7
-
27
-
-
34247170352
-
Polyamine-based analogues as biochemical probes and potential therapeutics
-
DOI 10.1042/BST0350356
-
Boncher, T.; Bi, X.; Varghese, S.; Casero, R.A., Jr.; Woster, P.M. Polyamine-based analogues as biochemical probes and potential therapeutics. Biochem. Soc. Trans., 2007, 35, 356-363. (Pubitemid 46596508)
-
(2007)
Biochemical Society Transactions
, vol.35
, Issue.2
, pp. 356-363
-
-
Boncher, T.1
Bi, X.2
Varghese, S.3
Casero Jr., R.A.4
Woster, P.M.5
-
28
-
-
43049129992
-
Polyaminohydroxamic acids and polyaminobenzamides as isoform selective histone deacetylase inhibitors
-
DOI 10.1021/jm701384x
-
Varghese, S.; Senanayake, T.; Murray-Stewart, T.; Doering, K.; Fraser, A.; Casero, R.A., Jr.; Woster, P.M. Polyaminohydroxamic acids and polyaminobenzamides as isoform selective histone deacetylase inhibitors. J. Med. Chem., 2008, 51, 2447-2456. (Pubitemid 351628506)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.8
, pp. 2447-2456
-
-
Varghese, S.1
Senanayake, T.2
Murray-Stewart, T.3
Doering, K.4
Fraser, A.5
Casero Jr., R.A.6
Woster, P.M.7
-
29
-
-
18344386053
-
Targeting therapeutic and imaging agents to folate receptor positive tumors
-
DOI 10.2174/1389201053642376
-
Reddy, J.A.; Allagadda, V.M.; Leamon, C.P. Targeting therapeutic and imaging agents to folate receptor positive tumors. Curr. Pharm. Biotechnol., 2005, 6, 131-150. (Pubitemid 40637386)
-
(2005)
Current Pharmaceutical Biotechnology
, vol.6
, Issue.2
, pp. 131-150
-
-
Reddy, J.A.1
Allagadda, V.M.2
Leamon, C.P.3
-
30
-
-
2442597872
-
Thiol-based SAHA analogues as potent histone deacetylase inhibitors
-
DOI 10.1016/j.bmcl.2004.03.063, PII S0960894X04004354
-
Suzuki, T.; Kouketsu, A.; Matsuura, A.; Kohara, A.; Ninomiya, S.; Kohda, K.; Miyata, N. Thiol-based SAHA analogues as potent histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2004, 14, 3313-3317. (Pubitemid 38624614)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.12
, pp. 3313-3317
-
-
Suzuki, T.1
Kouketsu, A.2
Matsuura, A.3
Kohara, A.4
Ninomiya, S.-I.5
Kohda, K.6
Miyata, N.7
-
31
-
-
34447093841
-
Design, synthesis, and biological activity of folate receptor-targeted prodrugs of thiolate histone deacetylase inhibitors
-
DOI 10.1016/j.bmcl.2007.05.040, PII S0960894X07005938
-
Suzuki, T.; Hisakawa, S.; Itoh, Y.; Suzuki, N.; Takahashi, K.; Kawahata, M.; Yamaguchi, K.; Nakagawa, H.; Miyata, N. Design, synthesis, and biological activity of folate receptor-targeted prodrugs of thiolate histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 4208-4212. (Pubitemid 47028601)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.15
, pp. 4208-4212
-
-
Suzuki, T.1
Hisakawa, S.2
Itoh, Y.3
Suzuki, N.4
Takahashi, K.5
Kawahata, M.6
Yamaguchi, K.7
Nakagawa, H.8
Miyata, N.9
-
32
-
-
79959348452
-
Novel folate-hydroxamate based antimetabolites: Synthesis and biological evaluation
-
Carrasco, M.P.; Enyedy, E.A.; Krupenko, N.I.; Krupenko, S.A.; Nuti, E.; Tuccinardi, T.; Santamaria, S.; Rossello, A.; Martinelli, A.; Santos, M.A. Novel folate-hydroxamate based antimetabolites: Synthesis and biological evaluation. Med. Chem., 2011, 7, 265-274.
-
(2011)
Med. Chem.
, vol.7
, pp. 265-274
-
-
Carrasco, M.P.1
Enyedy, E.A.2
Krupenko, N.I.3
Krupenko, S.A.4
Nuti, E.5
Tuccinardi, T.6
Santamaria, S.7
Rossello, A.8
Martinelli, A.9
Santos, M.A.10
-
33
-
-
62249169964
-
Differentiation therapy of acute myeloid leukemia: Past, present and future
-
Petrie, K.; Zelent, A.; Waxman, S. Differentiation therapy of acute myeloid leukemia: Past, present and future. Curr. Opin. Hematol., 2009, 16, 84-91.
-
(2009)
Curr. Opin. Hematol.
, vol.16
, pp. 84-91
-
-
Petrie, K.1
Zelent, A.2
Waxman, S.3
-
34
-
-
0242624636
-
Epigenetic targets in hematopoietic malignancies
-
Claus, R.; Lubbert, M. Epigenetic targets in hematopoietic malignancies. Oncogene, 2003, 22, 6489-6496. (Pubitemid 37372329)
-
(2003)
Oncogene
, vol.22
, Issue.43
, pp. 6489-6496
-
-
Claus, R.1
Lubbert, M.2
-
35
-
-
0035132140
-
Histone deacetylase-targeted treatment restores retinoic acid signaling and differentiation in acute myeloid leukemia
-
Ferrara, F.F.; Fazi, F.; Bianchini, A.; Padula, F.; Gelmetti, V.; Minucci, S.; Mancini, M.; Pelicci, P.G.; Lo Coco, F.; Nervi, C. Histone deacetylasetargeted treatment restores retinoic acid signaling and differentiation in acute myeloid leukemia. Cancer Res., 2001, 61, 2-7. (Pubitemid 32095688)
-
(2001)
Cancer Research
, vol.61
, Issue.1
, pp. 2-7
-
-
Ferrara, F.F.1
Fazi, F.2
Bianchini, A.3
Padula, F.4
Gelmetti, V.5
Minucci, S.6
Mancini, M.7
Pelicci, P.G.8
Lo Coco, F.9
Nervi, C.10
-
36
-
-
0036785378
-
Response to histone deacetylase inhibition of novel PML/RARalpha mutants detected in retinoic acid-resistant APL cells
-
Cote, S.; Rosenauer, A.; Bianchini, A.; Seiter, K.; Vandewiele, J.; Nervi, C.; Miller, W.H., Jr. Response to histone deacetylase inhibition of novel PML/RARalpha mutants detected in retinoic acid-resistant APL cells. Blood, 2002, 100, 2586-2596.
-
(2002)
Blood
, vol.100
, pp. 2586-2596
-
-
Cote, S.1
Rosenauer, A.2
Bianchini, A.3
Seiter, K.4
Vandewiele, J.5
Nervi, C.6
Miller Jr., W.H.7
-
37
-
-
0034721174
-
Novel mutual prodrug of retinoic and butyric acids with enhanced anticancer activity
-
DOI 10.1021/jm990540a
-
Nudelman, A.; Rephaeli, A. Novel mutual prodrug of retinoic and butyric acids with enhanced anticancer activity. J. Med. Chem., 2000, 43, 2962-2966. (Pubitemid 30599654)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.15
, pp. 2962-2966
-
-
Nudelman, A.1
Rephaeli, A.2
-
38
-
-
0142089014
-
A retinoid/butyric acid prodrug overcomes retinoic acid resistance in leukemias by induction of apoptosis
-
Mann, K.K.; Rephaeli, A.; Colosimo, A.L.; Diaz, Z.; Nudelman, A.; Levovich, I.; Jing, Y.; Waxman, S.; Miller, W.H., Jr. A retinoid/butyric acid prodrug overcomes retinoic acid resistance in leukemias by induction of apoptosis. Mol. Cancer Res., 2003, 1, 903-912. (Pubitemid 37288708)
-
(2003)
Molecular Cancer Research
, vol.1
, Issue.12
, pp. 903-912
-
-
Mann, K.K.1
Rephaeli, A.2
Colosimo, A.L.3
Diaz, Z.4
Nudelman, A.5
Levovich, I.6
Jing, Y.7
Waxman, S.8
Miller Jr., W.H.9
-
39
-
-
46849096306
-
Design, synthesis, and evaluation of novel mutual prodrugs (hybrid drugs) of all-trans-retinoic acid and histone deacetylase inhibitors with enhanced anticancer activities in breast and prostate cancer cells in vitro
-
DOI 10.1021/jm8001839
-
Gediya, L.K.; Khandelwal, A.; Patel, J.; Belosay, A.; Sabnis, G.; Mehta, J.; Purushottamachar, P.; Njar, V.C. Design, synthesis, and evaluation of novel mutual prodrugs (hybrid drugs) of all-trans-retinoic acid and histone deacetylase inhibitors with enhanced anticancer activities in breast and prostate cancer cells in vitro. J. Med. Chem., 2008, 51, 3895-3904. (Pubitemid 351956518)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.13
, pp. 3895-3904
-
-
Gediya, L.K.1
Khandelwal, A.2
Patel, J.3
Belosay, A.4
Sabnis, G.5
Mehta, J.6
Purushottamachar, P.7
Njar, V.C.O.8
-
40
-
-
64049097460
-
Microtubule dynamics as a target in oncology
-
Risinger, A.L.; Giles, F.J.; Mooberry, S.L. Microtubule dynamics as a target in oncology. Cancer Treat. Rev., 2009, 35, 255-261.
-
(2009)
Cancer Treat. Rev.
, vol.35
, pp. 255-261
-
-
Risinger, A.L.1
Giles, F.J.2
Mooberry, S.L.3
-
41
-
-
0037416151
-
HDAC-6 interacts with and deacetylates tubulin and microtubules in vivo
-
DOI 10.1093/emboj/cdg115
-
Zhang, Y.; Li, N.; Caron, C.; Matthias, G.; Hess, D.; Khochbin, S.; Matthias, P. HDAC-6 interacts with and deacetylates tubulin and microtubules in vivo. EMBO J., 2003, 22, 1168-1179. (Pubitemid 36313600)
-
(2003)
EMBO Journal
, vol.22
, Issue.5
, pp. 1168-1179
-
-
Zhang, Y.1
Li, N.2
Caron, C.3
Matthias, G.4
Hess, D.5
Khochbin, S.6
Matthias, P.7
-
42
-
-
33845209109
-
Histone deacetylase inhibitors and paclitaxel cause synergistic effects on apoptosis and microtubule stabilization in papillary serous endometrial cancer cells
-
DOI 10.1158/1535-7163.MCT-06-0209
-
Dowdy, S.C.; Jiang, S.; Zhou, X.C.; Hou, X.; Jin, F.; Podratz, K.C.; Jiang, S.W. Histone deacetylase inhibitors and paclitaxel cause synergistic effects on apoptosis and microtubule stabilization in papillary serous endometrial cancer cells. Mol. Cancer Ther., 2006, 5, 2767-2776. (Pubitemid 44849003)
-
(2006)
Molecular Cancer Therapeutics
, vol.5
, Issue.11
, pp. 2767-2776
-
-
Dowdy, S.C.1
Jiang, S.2
Zhou, X.C.3
Hou, X.4
Jin, F.5
Podratz, K.C.6
Jiang, S.-W.7
-
43
-
-
35948965312
-
Valproic acid enhances tubulin acetylation and apoptotic activity of paclitaxel on anaplastic thyroid cancer cell lines
-
DOI 10.1677/ERC-07-0096
-
Catalano, M.G.; Poli, R.; Pugliese, M.; Fortunati, N.; Boccuzzi, G. Valproic acid enhances tubulin acetylation and apoptotic activity of paclitaxel on anaplastic thyroid cancer cell lines. Endocr. Relat. Cancer, 2007, 14, 839-845. (Pubitemid 350074071)
-
(2007)
Endocrine-Related Cancer
, vol.14
, Issue.3
, pp. 839-845
-
-
Catalano, M.G.1
Poli, R.2
Pugliese, M.3
Fortunati, N.4
Boccuzzi, G.5
-
44
-
-
73949140461
-
Carboplatin and Paclitaxel in combination with either vorinostat or placebo for first-line therapy of advanced non-small-cell lung cancer
-
Ramalingam, S.S.; Maitland, M.L.; Frankel, P.; Argiris, A.E.; Koczywas, M.; Gitlitz, B.; Thomas, S.; Espinoza-Delgado, I.; Vokes, E.E.; Gandara, D.R.; Belani, C.P. Carboplatin and Paclitaxel in combination with either vorinostat or placebo for first-line therapy of advanced non-small-cell lung cancer. J. Clin. Oncol., 2010, 28, 56-62.
-
(2010)
J. Clin. Oncol.
, vol.28
, pp. 56-62
-
-
Ramalingam, S.S.1
Maitland, M.L.2
Frankel, P.3
Argiris, A.E.4
Koczywas, M.5
Gitlitz, B.6
Thomas, S.7
Espinoza-Delgado, I.8
Vokes, E.E.9
Gandara, D.R.10
Belani, C.P.11
-
45
-
-
71049188845
-
Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compounds
-
Passarella, D.; Comi, D.; Vanossi, A.; Paganini, G.; Colombo, F.; Ferrante, L.; Zuco, V.; Danieli, B.; Zunino, F. Histone deacetylase and microtubules as targets for the synthesis of releasable conjugate compounds. Bioorg. Med. Chem. Lett., 2009, 19, 6358-6363.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6358-6363
-
-
Passarella, D.1
Comi, D.2
Vanossi, A.3
Paganini, G.4
Colombo, F.5
Ferrante, L.6
Zuco, V.7
Danieli, B.8
Zunino, F.9
-
46
-
-
37249026623
-
Recent developments in the field of anticancer platinum complexes
-
Galanski, M. Recent developments in the field of anticancer platinum complexes. Recent Pat. Anticancer Drug Discov., 2006, 1, 285-295.
-
(2006)
Recent Pat. Anticancer Drug Discov.
, vol.1
, pp. 285-295
-
-
Galanski, M.1
-
47
-
-
70449345822
-
A novel anti-cancer bifunctional platinum drug candidate with dual DNA binding and histone deacetylase inhibitory activity
-
Griffith, D.; Morgan, M.P.; Marmion, C.J. A novel anti-cancer bifunctional platinum drug candidate with dual DNA binding and histone deacetylase inhibitory activity. Chem. Commun., 2009, 6735-6737.
-
(2009)
Chem. Commun.
, pp. 6735-6737
-
-
Griffith, D.1
Morgan, M.P.2
Marmion, C.J.3
-
48
-
-
34547122494
-
HDAC inhibitors: Clinical update and mechanism-based potential
-
DOI 10.1016/j.bcp.2007.04.007, PII S0006295207002262
-
Glaser, K.B. HDAC inhibitors: Clinical update and mechanism-based potential. Biochem. Pharmacol., 2007, 74, 659-671. (Pubitemid 47096639)
-
(2007)
Biochemical Pharmacology
, vol.74
, Issue.5
, pp. 659-671
-
-
Glaser, K.B.1
-
49
-
-
68949166379
-
Phase 1 dose-escalation study of oral tyrosine kinase inhibitor masitinib in advanced and/or metastatic solid cancers
-
Soria, J.C.; Massard, C.; Magne, N.; Bader, T.; Mansfield, C.D.; Blay, J.Y.; Bui, B.N.; Moussy, A.; Hermine, O.; Armand, J.P. Phase 1 dose-escalation study of oral tyrosine kinase inhibitor masitinib in advanced and/or metastatic solid cancers. Eur. J. Cancer, 2009, 45, 2333-2341.
-
(2009)
Eur. J. Cancer
, vol.45
, pp. 2333-2341
-
-
Soria, J.C.1
Massard, C.2
Magne, N.3
Bader, T.4
Mansfield, C.D.5
Blay, J.Y.6
Bui, B.N.7
Moussy, A.8
Hermine, O.9
Armand, J.P.10
-
50
-
-
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
-
Mahboobi, S.; Dove, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; Maier, T.; Beckers, T. 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., 2009, 52, 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
-
51
-
-
77955229921
-
Chimeric tyrosine kinase-HDAC inhibitors as antiproliferative agents
-
Uecker, A.; Sicker, M.; Beckers, T.; Mahboobi, S.; Hagerstrand, D.; Ostman, A.; Bohmer, F.D. Chimeric tyrosine kinase-HDAC inhibitors as antiproliferative agents. Anticancer Drugs, 2010, 21, 759-765.
-
(2010)
Anticancer Drugs
, vol.21
, pp. 759-765
-
-
Uecker, A.1
Sicker, M.2
Beckers, T.3
Mahboobi, S.4
Hagerstrand, D.5
Ostman, A.6
Bohmer, F.D.7
-
52
-
-
77949353758
-
Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N- hydroxyheptanamide (CUDC-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
-
Cai, X.; Zhai, H.X.; Wang, J.; Forrester, J.; Qu, H.; Yin, L.; Lai, C.J.; Bao, R.; Qian, C. Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin- 6-yloxy)-N-hydroxyheptanamide (CUDC-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer. J. Med. Chem., 2010, 53, 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
-
53
-
-
51849144627
-
Knowledge based prediction of ligand binding modes and rational inhibitor design for kinase drug discovery
-
Ghose, A.K.; Herbertz, T.; Pippin, D.A.; Salvino, J.M.; Mallamo, J.P. Knowledge based prediction of ligand binding modes and rational inhibitor design for kinase drug discovery. J. Med. Chem., 2008, 51, 5149-5171.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5149-5171
-
-
Ghose, A.K.1
Herbertz, T.2
Pippin, D.A.3
Salvino, J.M.4
Mallamo, J.P.5
-
54
-
-
33846899405
-
Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors
-
DOI 10.1021/jm0608107
-
Liao, J.J. Molecular recognition of protein kinase binding pockets for design of potent and selective kinase inhibitors. J. Med. Chem., 2007, 50, 409-424. (Pubitemid 46239775)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.3
, pp. 409-424
-
-
Liao, J.J.-L.1
-
55
-
-
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
-
56
-
-
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
-
Mahboobi, S.; Sellmer, A.; Winkler, M.; Eichhorn, E.; Pongratz, H.; Ciossek, T.; Baer, T.; Maier, T.; Beckers, T. 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., 2010, 53, 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
-
57
-
-
67650649489
-
IMP dehydrogenase: Structure, mechanism, and inhibition
-
Hedstrom, L. IMP dehydrogenase: Structure, mechanism, and inhibition. Chem. Rev., 2009, 109, 2903-2928.
-
(2009)
Chem. Rev.
, vol.109
, pp. 2903-2928
-
-
Hedstrom, L.1
-
58
-
-
34447642328
-
Recent development of IMP dehydrogenase inhibitors for the treatment of cancer
-
Chen, L.; Pankiewicz, K.W. Recent development of IMP dehydrogenase inhibitors for the treatment of cancer. Curr. Opin. Drug Discov. Devel., 2007, 10, 403-412. (Pubitemid 47093123)
-
(2007)
Current Opinion in Drug Discovery and Development
, vol.10
, Issue.4
, pp. 403-412
-
-
Chen, L.1
Pankiewicz, K.W.2
-
59
-
-
42049105745
-
Nicotinamide adenine dinucleotide based therapeutics
-
DOI 10.2174/092986708783885282
-
Chen, L.; Petrelli, R.; Felczak, K.; Gao, G.; Bonnac, L.; Yu, J.S.; Bennett, E.M.; Pankiewicz, K.W. Nicotinamide adenine dinucleotide based therapeutics. Curr. Med. Chem., 2008, 15, 650-670. (Pubitemid 351516802)
-
(2008)
Current Medicinal Chemistry
, vol.15
, Issue.7
, pp. 650-670
-
-
Chen, L.1
Petrelli, R.2
Felczak, K.3
Gao, G.4
Bonnac, L.5
Yu, J.S.6
Bennett, E.M.7
Pankicwicz, K.W.8
-
60
-
-
0034121721
-
The structure of inosine 5'-monophosphate dehydrogenase and the design of novel inhibitors
-
DOI 10.1016/S0162-3109(00)00193-4, PII S0162310900001934
-
Sintchak, M.D.; Nimmesgern, E. The structure of inosine 5 '-monophosphate dehydrogenase and the design of novel inhibitors. Immunopharmacology, 2000, 47, 163-184. (Pubitemid 30394537)
-
(2000)
Immunopharmacology
, vol.47
, Issue.2-3
, pp. 163-184
-
-
Sintchak, M.D.1
Nimmesgern, E.2
-
61
-
-
0036720880
-
Characterization of pharmacological efficacy of VX-148, a new, potent immunosuppressive inosine 5'-monophosphate dehydrogenase inhibitor
-
DOI 10.1124/jpet.102.035659
-
Jain, J.; Almquist, S.J.; Heiser, A.D.; Shlyakhter, D.; Leon, E.; Memmott, C.; Moody, C.S.; Nimmesgern, E.; Decker, C. Characterization of pharmacological efficacy of VX-148, a new, potent immunosuppressive inosine 5'-monophosphate dehydrogenase inhibitor. J. Pharmacol. Exp. Ther., 2002, 302, 1272-1277. (Pubitemid 34920252)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.302
, Issue.3
, pp. 1272-1277
-
-
Jain, J.1
Almquist, S.J.2
Heiser, A.D.3
Shlyakhter, D.4
Leon, E.5
Memmott, C.6
Moody, C.S.7
Nimmesgern, E.8
Decker, C.9
-
62
-
-
0037131761
-
The TosMIC approach to 3-(oxazol-5-yl) indoles: Application to the synthesis of indole-based IMPDH inhibitors
-
DOI 10.1016/S0960-894X(02)00748-5, PII S0960894X02007485
-
Dhar, T.G.M.; Shen, Z.Q.; Fleener, C.A.; Rouleau, K.A.; Barrish, J.C.; Hollenbaugh, D.L.; Iwanowicz, E.J. The TosMIC approach to 3-(oxazol-5-yl) indoles: Application to the synthesis of indole-based IMPDH inhibitors. Bioorg. Med. Chem. Lett., 2002, 12, 3305-3308. (Pubitemid 35248236)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.22
, pp. 3305-3308
-
-
Dhar T.G.Murali1
Shen, Z.2
Fleener, C.A.3
Rouleau, K.A.4
Barrish, J.C.5
Hollenbaugh, D.L.6
Iwanowicz, E.J.7
-
63
-
-
1842551076
-
3-Cyanoindole-based inhibitors of inosine monophosphate dehydrogenase: Synthesis and initial structure-activity relationships
-
DOI 10.1016/S0960-894X(03)00757-1
-
Dhar, T.G.M.; Shen, Z.Q.; Gu, H.H.; Chen, P.; Norris, D.; Watterson, S.H.; Ballentine, S.K.; Fleener, C.A.; Rouleau, K.A.; Barrish, J.C.; Townsend, R.; Hollenbaugh, D.L.; Iwanowicz, E.J. 3-cyanoindole-based inhibitors of inosine monophosphate dehydrogenase: Synthesis and initial structureactivity relationships. Bioorg. Med. Chem. Lett., 2003, 13, 3557-3560. (Pubitemid 37141429)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.20
, pp. 3557-3560
-
-
Dhar, T.G.M.1
Shen, Z.2
Gu, H.H.3
Chen, P.4
Norris, D.5
Watterson, S.H.6
Ballentine, S.K.7
Fleener, C.A.8
Rouleau, K.A.9
Barrish, J.C.10
Townsend, R.11
Hollenbaugh, D.L.12
Iwanowicz, E.J.13
-
64
-
-
0037424684
-
Identification of novel and potent isoquinoline aminooxazole-based IMPDH inhibitors
-
DOI 10.1016/S0960-894X(03)00107-0
-
Chen, P.; Norris, D.; Haslow, K.D.; Dhar, T.G.M.; Pitts, W.J.; Watterson, S.H.; Cheney, D.L.; Bassolino, D.A.; Fleener, C.A.; Rouleau, K.A.; Hollenbaugh, D.L.; Townsend, R.M.; Barrish, J.C.; Iwanowicz, E.J. Identification of novel and potent isoquinoline aminooxazole-based IMPDH inhibitors. Bioorg. Med. Chem. Lett., 2003, 13, 1345-1348. (Pubitemid 36351349)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.7
, pp. 1345-1348
-
-
Chen, P.1
Norris, D.2
Haslow, K.D.3
Dhar, T.G.M.4
Pitts, W.J.5
Watterson, S.H.6
Cheney, D.L.7
Bassolino, D.A.8
Fleener, C.A.9
Rouleau, K.A.10
Hollenbaugh, D.L.11
Townsend, R.M.12
Barrish, J.C.13
Iwanowicz, E.J.14
-
65
-
-
34547610513
-
Acridone-based inhibitors of inosine 5'-monophosphate dehydrogenase: Discovery and SAR leading to the identification of N-(2-(6-(4-ethylpiperazin-1- yl)pyridin-3-yl)propan-2-yl)-2-fluoro-9-oxo-9,10-dihydroacridine-3-carboxamide (BMS-566419)
-
DOI 10.1021/jm070299x
-
Watterson, S.H.; Chen, P.; Zhao, Y.; Gu, H.H.; Dhar, T.G.; Xiao, Z.; Ballentine, S.K.; Shen, Z.; Fleener, C.A.; Rouleau, K.A.; Obermeier, M.; Yang, Z.; McIntyre, K.W.; Shuster, D.J.; Witmer, M.; Dambach, D.; Chao, S.; Mathur, A.; Chen, B.C.; Barrish, J.C.; Robl, J.A.; Townsend, R.; Iwanowicz, E.J. Acridone-based inhibitors of inosine 5'-monophosphate dehydrogenase: Discovery and SAR leading to the identification of N-(2-(6-(4-ethylpiperazin-1-yl)pyridin- 3-yl)propan-2-yl)-2-fluoro-9-oxo-9,10-dihydroacridine-3-carboxamide (BMS-566419). J. Med. Chem., 2007, 50, 3730-3742. (Pubitemid 47195479)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.15
, pp. 3730-3742
-
-
Watterson, S.H.1
Chen, P.2
Zhao, Y.3
Gu, H.H.4
Dhar, T.G.M.5
Xiao, Z.6
Ballentine, S.K.7
Shen, Z.8
Fleener, C.A.9
Rouleau, K.A.10
Obermeier, M.11
Yang, Z.12
McIntyre, K.W.13
Shuster, D.J.14
Witmer, M.15
Dambach, D.16
Chao, S.17
Mathur, A.18
Chen, B.-C.19
Barrish, J.C.20
Robl, J.A.21
Townsend, R.22
Iwanowicz, E.J.23
more..
-
66
-
-
18644380984
-
Novel amide-based inhibitors of inosine 5'-monophosphate dehydrogenase
-
DOI 10.1016/S0960-894X(02)00601-7, PII S0960894X02006017
-
Watterson, S.H.; Liu, C.J.; Dhar, T.G.M.; Gu, H.H.; Pitts, W.J.; Barrish, J.C.; Fleener, C.A.; Rouleau, K.; Sherbina, N.Z.; Hollenbaugh, D.L.; Iwanowicz, E.J. Novel amide-based inhibitors of inosine 5 '-monophosphate dehydrogenase. Bioorg. Med. Chem. Lett., 2002, 12, 2879-2882. (Pubitemid 35266754)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.20
, pp. 2879-2882
-
-
Watterson, S.H.1
Liu, C.2
Dhar T.G.Murali3
Gu, H.H.4
Pitts, W.J.5
Barrish, J.C.6
Fleener, C.A.7
Rouleau, K.8
Sherbina, N.Z.9
Hollenbaugh, D.L.10
Iwanowicz, E.J.11
-
67
-
-
12444342502
-
Novel diamide-based inhibitors of IMPDH
-
DOI 10.1016/S0960-894X(02)00132-4, PII S0960894X02001324
-
Gu, H.H.; Iwanowicz, E.J.; Guo, J.Q.; Watterson, S.H.; Shen, Z.Q.; Pitts, W.J.; Dhar, T.G.M.; Fleener, C.A.; Rouleau, K.; Sherbina, N.Z.; Witmer, M.; Tredup, J.; Hollenbaugh, D. Novel diamide-based inhibitors of IMPDH. Bioorg. Med. Chem. Lett., 2002, 12, 1323-1326. (Pubitemid 34327509)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.9
, pp. 1323-1326
-
-
Gu, H.H.1
Iwanowicz, E.J.2
Guo, J.3
Watterson, S.H.4
Shen, Z.5
Pitts, W.J.6
Dhar T.G.Murali7
Fleener, C.A.8
Rouleau, K.9
Sherbina, N.Z.10
Witmer, M.11
Tredup, J.12
Hollenbaugh, D.13
-
68
-
-
18644379690
-
Novel guanidine-Based inhibitors of inosine monophosphate dehydrogenase
-
DOI 10.1016/S0960-894X(02)00600-5, PII S0960894X02006005
-
Iwanowicz, E.J.; Watterson, S.H.; Liu, C.J.; Gu, H.H.; Mitt, T.; Leftheris, K.; Barrish, J.C.; Fleener, C.A.; Rouleau, K.; Sherbina, N.Z.; Hollenbaugh, D.L. Novel guanidine-based inhibitors of inosine monophosphate dehydrogenase. Bioorg. Med. Chem. Lett., 2002, 12, 2931-2934. (Pubitemid 35266762)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.20
, pp. 2931-2934
-
-
Iwanowicz, E.J.1
Watterson, S.H.2
Liu, C.3
Gu, H.H.4
Mitt, T.5
Leftheris, K.6
Barrish, J.C.7
Fleener, C.A.8
Rouleau, K.9
Sherbina, N.Z.10
Hollenbaugh, D.L.11
-
69
-
-
18444369935
-
Rapid synthesis of triazine inhibitors of inosine monophosphate dehydrogenase
-
DOI 10.1016/S0960-894X(02)00351-7, PII S0960894X02003517
-
Pitts, W.J.; Guo, J.Q.; Dhar, T.G.M.; Shen, Z.Q.; Gu, H.H.; Watterson, S.H.; Bednarz, M.S.; Chen, B.C.; Barrish, J.C.; Bassolino, D.; Cheney, D.; Fleener, C.A.; Rouleau, K.A.; Hollenbaugh, D.L.; Iwanowicz, E.J. Rapid synthesis oftriazine inhibitors of inosine monophosphate dehydrogenase. Bioorg. Med. Chem. Lett., 2002, 12, 2137-2140. (Pubitemid 34804384)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.16
, pp. 2137-2140
-
-
Pitts, W.J.1
Guo, J.2
Dhar T.G.Murali3
Shen, Z.4
Gu, H.H.5
Watterson, S.H.6
Bednarz, M.S.7
Chen, B.-C.8
Barrish, J.C.9
Bassolino, D.10
Cheney, D.11
Fleener, C.A.12
Rouleau, K.A.13
Hollenbaugh, D.L.14
Iwanowicz, E.J.15
-
70
-
-
12444346848
-
Inhibitors of inosine monophosphate dehydrogenase: SARs about the N-[3-methoxy-4-(5-oxazolyl)phenyl moiety
-
DOI 10.1016/S0960-894X(03)00258-0
-
Iwanowicz, E.J.; Watterson, S.H.; Guo, J.Q.; Pitts, W.J.; Dhar, T.G.M.; Shen, Z.Q.; Chen, P.; Gu, H.H.; Fleener, C.A.; Rouleau, K.A.; Cheney, D.L.; Townsend, R.M.; Hollenbaugh, D.L. Inhibitors of inosine monophosphate dehydrogenase: SARs about the N-3-methoxy-4-(5-oxazolyl)phenyl moiety. Bioorg. Med. Chem. Lett., 2003, 13, 2059-2063. (Pubitemid 36638410)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.12
, pp. 2059-2063
-
-
Iwanowicz, E.J.1
Watterson, S.H.2
Guo, J.3
Pitts, W.J.4
Murali Dhar, T.G.5
Shen, Z.6
Chen, P.7
Gu, H.H.8
Fleener, C.A.9
Rouleau, K.A.10
Cheney, D.L.11
Townsend, R.M.12
Hollenbaugh, D.L.13
-
71
-
-
0037161583
-
Discovery of N-[2-[2-[[3-methoxy-4-(5-oxazolyl)phenyl]-amino]-5-oxazolyl] phenyl]-N- methyl-4-morpholinea0cetamide as a novel and potent inhibitor of inosine monophosphate dehydrogenase with excellent in vivo activity
-
DOI 10.1021/jm0105777
-
Dhar, T.G.M.; Shen, Z.Q.; Guo, J.Q.; Liu, C.J.; Watterson, S.H.; Gu, H.H.; Pitts, W.J.; Fleener, C.A.; Rouleau, K.A.; Sherbina, N.Z.; McIntyre, K.W.; Shuster, D.J.; Witmer, M.R.; Tredup, J.A.; Chen, B.C.; Zhao, R.L.; Bednarz, M.S.; Cheney, D.L.; MacMaster, J.F.; Miller, L.M.; Berry, K.K.; Harper, T.W.; Barrish, J.C.; Hollenbaugh, D.L.; Iwanowicz, E.J. Discovery of N-2-2-3-methoxy-4-(5-oxazolyl)phenyl amino -5-oxazolyl phenyl -N-methyl-4-morpholineacetamide as a novel and potent inhibitor of inosine monophosphate dehydrogenase (IMPDH) with excellent in vivo activity. J. Med. Chem., 2002, 45, 2127-2130. (Pubitemid 34525792)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.11
, pp. 2127-2130
-
-
Dhar, T.G.M.1
Shen, Z.2
Guo, J.3
Liu, C.4
Watterson, S.H.5
Gu, H.H.6
Pitts, W.J.7
Fleener, C.A.8
Rouleau, K.A.9
Sherbina, N.Z.10
McIntyre, K.W.11
Witmer, M.R.12
Tredup, J.A.13
Chen, B.-C.14
Zhao, R.15
Bednarz, M.S.16
Cheney, D.L.17
MacMaster, J.F.18
Miller, L.M.19
Berry, K.K.20
Harper, T.W.21
Barrish, J.C.22
Hollenbaugh, D.L.23
Iwanowicz, E.J.24
more..
-
72
-
-
0037328362
-
Novel inhibitors of IMPDH: A highly potent and selective quinolone-based series
-
DOI 10.1016/S0960-894X(02)00944-7, PII S0960894X02009447
-
Watterson, S.H.; Carlsen, M.; Dhar, T.G.M.; Shen, Z.Q.; Pitts, W.J.; Guo, J.Q.; Gu, H.H.; Norris, D.; Chorba, J.; Chen, P.; Cheney, D.; Witmer, M.; Fleener, C.A.; Rouleau, K.; Townsend, R.; Hollenbaugh, D.L.; Iwanowicz, E.J. Novel inhibitors of IMPDH: A highly potent and selective quinolonebased series. Bioorg. Med. Chem. Lett., 2003, 13, 543-546. (Pubitemid 36259731)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.3
, pp. 543-546
-
-
Watterson, S.H.1
Carlsen, M.2
Dhar, T.G.M.3
Shen, Z.4
Pitts, W.J.5
Guo, J.6
Gu, H.H.7
Norris, D.8
Chorba, J.9
Chen, P.10
Cheney, D.11
Witmer, M.12
Fleener, C.A.13
Rouleau, K.14
Townsend, R.15
Hollenbaugh, D.L.16
Iwanowicz, E.J.17
-
73
-
-
0037424695
-
Novel indole-based inhibitors of IMPDH: Introduction of hydrogen bond acceptors at indole C-3
-
DOI 10.1016/S0960-894X(03)00109-4
-
Watterson, S.H.; Dhar, T.G.M.; Ballentine, S.K.; Shen, Z.Q.; Barrish, J.C.; Cheney, D.; Fleener, C.A.; Rouleau, K.A.; Townsend, R.; Hollenbaugh, D.L.; Iwanowicz, E.J. Novel indole-based inhibitors of IMPDH: Introduction of hydrogen bond acceptors at indole C-3. Bioorg. Med. Chem. Lett., 2003, 13, 1273-1276. (Pubitemid 36351332)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.7
, pp. 1273-1276
-
-
Watterson, S.H.1
Dhar, T.G.M.2
Ballentine, S.K.3
Shen, Z.4
Barrish, J.C.5
Cheney, D.6
Fleener, C.A.7
Rouleau, K.A.8
Townsend, R.9
Hollenbaugh, D.L.10
Iwanowicz, E.J.11
-
74
-
-
19944431381
-
Quinazolinethiones and quinazolinediones, novel inhibitors of inosine monophosphate dehydrogenase: Synthesis and initial structure-activity relationships
-
DOI 10.1016/j.bmcl.2004.11.015, PII S0960894X04013514
-
Buckley, G.M.; Davies, N.; Dyke, H.J.; Gilbert, P.J.; Hannah, D.R.; Haughan, A.F.; Hunt, C.A.; Pitt, W.R.; Profit, R.H.; Ray, N.C.; Richard, M.D.; Sharpe, A.; Taylor, A.J.; Whitworth, J.M.; Williams, S.C. Quinazolinethiones and quinazolinediones, novel inhibitors of inosine monophosphate dehydrogenase: Synthesis and initial structure-activity relationships. Bioorg. Med. Chem. Lett., 2005, 15, 751-754. (Pubitemid 40143160)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.3
, pp. 751-754
-
-
Buckley, G.M.1
Davies, N.2
Dyke, H.J.3
Gilbert, P.J.4
Hannah, D.R.5
Haughan, A.F.6
Hunt, C.A.7
Pitt, W.R.8
Profit, R.H.9
Ray, N.C.10
Richard, M.D.11
Sharpe, A.12
Taylor, A.J.13
Whitworth, J.M.14
Williams, S.C.15
-
75
-
-
37349017604
-
Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylases for cancer treatment
-
DOI 10.1021/jm070864w
-
Chen, L.; Wilson, D.; Jayaram, H.N.; Pankiewicz, K.W. Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylases for cancer treatment. J. Med. Chem., 2007, 50, 6685-6691. (Pubitemid 350309105)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.26
, pp. 6685-6691
-
-
Chen, L.1
Wilson, D.2
Jayaram, H.N.3
Pankiewicz, K.W.4
-
76
-
-
55049101683
-
Hydroxamic acid derivatives of mycophenolic acid inhibit histone deacetylase at the cellular level
-
Batovska, D.I.; Kim, D.H.; Mitsuhashi, S.; Cho, Y.S.; Kwon, H.J.; Ubukata, M. Hydroxamic acid derivatives of mycophenolic acid inhibit histone deacetylase at the cellular level. Biosci. Biotechnol. Biochem., 2008, 72, 2623-2631.
-
(2008)
Biosci. Biotechnol. Biochem.
, vol.72
, pp. 2623-2631
-
-
Batovska, D.I.1
Kim, D.H.2
Mitsuhashi, S.3
Cho, Y.S.4
Kwon, H.J.5
Ubukata, M.6
-
77
-
-
78449253588
-
Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase and differentiation induction of K562 cells among the mycophenolic acid derivatives
-
Mitsuhashi, S.; Takenaka, J.; Iwamori, K.; Nakajima, N.; Ubukata, M. Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase and differentiation induction of K562 cells among the mycophenolic acid derivatives. Bioorg. Med. Chem., 2010, 18, 8106-8111.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 8106-8111
-
-
Mitsuhashi, S.1
Takenaka, J.2
Iwamori, K.3
Nakajima, N.4
Ubukata, M.5
-
78
-
-
77955466735
-
Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylase based on a cinnamic hydroxamic acid core structure
-
Chen, L.; Petrelli, R.; Gao, G.; Wilson, D.J.; McLean, G.T.; Jayaram, H.N.; Sham, Y.Y.; Pankiewicz, K.W. Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylase based on a cinnamic hydroxamic acid core structure. Bioorg. Med. Chem., 2010, 18, 5950-5964.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 5950-5964
-
-
Chen, L.1
Petrelli, R.2
Gao, G.3
Wilson, D.J.4
McLean, G.T.5
Jayaram, H.N.6
Sham, Y.Y.7
Pankiewicz, K.W.8
|