-
1
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
Jordan, M. A.; Wilson, L. Microtubules as a target for anticancer drugs Nat. Rev. Cancer 2004, 4, 253 10.1038/nrc1317
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 253
-
-
Jordan, M.A.1
Wilson, L.2
-
2
-
-
64749094310
-
The cancer genome
-
Stratton, M. R.; Campbell, P. J.; Futreal, P. A. The cancer genome Nature 2009, 458, 719 10.1038/nature07943
-
(2009)
Nature
, vol.458
, pp. 719
-
-
Stratton, M.R.1
Campbell, P.J.2
Futreal, P.A.3
-
3
-
-
84890111958
-
Immune-based mechanisms of cytotoxic chemotherapy: Implications for the design of novel and rationale-based combined treatments against cancer
-
Bracci, L.; Schiavoni, G.; Sistigu, A.; Belardelli, F. Immune-based mechanisms of cytotoxic chemotherapy: implications for the design of novel and rationale-based combined treatments against cancer Cell Death Differ. 2014, 21, 15 10.1038/cdd.2013.67
-
(2014)
Cell Death Differ.
, vol.21
, pp. 15
-
-
Bracci, L.1
Schiavoni, G.2
Sistigu, A.3
Belardelli, F.4
-
4
-
-
80053154666
-
Pharmacokinetic optimization of 4-substituted methoxybenzoyl-aryl-thiazole and 2-aryl-4-benzoyl-imidazole for improving oral bioavailability
-
Li, C. M.; Chen, J.; Lu, Y.; Narayanan, R.; Parke, D. N.; Li, W.; Ahn, S.; Miller, D. D.; Dalton, J. T. Pharmacokinetic optimization of 4-substituted methoxybenzoyl-aryl-thiazole and 2-aryl-4-benzoyl-imidazole for improving oral bioavailability Drug Metab. Dispos. 2011, 39, 1833 10.1124/dmd.110.036616
-
(2011)
Drug Metab. Dispos.
, vol.39
, pp. 1833
-
-
Li, C.M.1
Chen, J.2
Lu, Y.3
Narayanan, R.4
Parke, D.N.5
Li, W.6
Ahn, S.7
Miller, D.D.8
Dalton, J.T.9
-
5
-
-
0034811602
-
Correlation of gene expression of ten drug efflux proteins of the ATP-binding cassette transporter family in normal human jejunum and in human intestinal epithelial Caco-2 cell monolayers
-
Taipalensuu, J.; Tornblom, H.; Lindberg, G.; Einarsson, C.; Sjoqvist, F.; Melhus, H.; Garberg, P.; Sjostrom, B.; Lundgren, B.; Artursson, P. Correlation of gene expression of ten drug efflux proteins of the ATP-binding cassette transporter family in normal human jejunum and in human intestinal epithelial Caco-2 cell monolayers J. Pharmacol. Exp. Ther. 2001, 299, 2001
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.299
, pp. 2001
-
-
Taipalensuu, J.1
Tornblom, H.2
Lindberg, G.3
Einarsson, C.4
Sjoqvist, F.5
Melhus, H.6
Garberg, P.7
Sjostrom, B.8
Lundgren, B.9
Artursson, P.10
-
6
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Delivery Rev. 2001, 46, 3 10.1016/S0169-409X(00)00129-0
-
(2001)
Adv. Drug Delivery Rev.
, vol.46
, pp. 3
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
7
-
-
84871643254
-
Synthesis and biological evaluation of colchicine B-ring analogues tethered with halogenated benzyl moieties
-
Cosentino, L.; Redondo-Horcajo, M.; Zhao, Y.; Santos, A. R.; Chowdury, K. F.; Vinader, V.; Abdallah, Q. M.; Abdel-Rahman, H.; Fournier-Dit-Chabert, J.; Shnyder, S. D.; Loadman, P. M.; Fang, W. S.; Diaz, J. F.; Barasoain, I.; Burns, P. A.; Pors, K. Synthesis and biological evaluation of colchicine B-ring analogues tethered with halogenated benzyl moieties J. Med. Chem. 2012, 55, 11062 10.1021/jm301151t
-
(2012)
J. Med. Chem.
, vol.55
, pp. 11062
-
-
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.9
Shnyder, S.D.10
Loadman, P.M.11
Fang, W.S.12
Diaz, J.F.13
Barasoain, I.14
Burns, P.A.15
Pors, K.16
-
8
-
-
84870248825
-
Synthesis and biological evaluation of colchicine C-ring analogues tethered with aliphatic linkers suitable for prodrug derivatisation
-
Fournier-Dit-Chabert, J.; Vinader, V.; Santos, A. R.; Redondo-Horcajo, M.; Dreneau, A.; Basak, R.; Cosentino, L.; Marston, G.; Abdel-Rahman, H.; Loadman, P. M.; Shnyder, S. D.; Diaz, J. F.; Barasoain, I.; Falconer, R. A.; Pors, K. Synthesis and biological evaluation of colchicine C-ring analogues tethered with aliphatic linkers suitable for prodrug derivatisation Bioorg. Med. Chem. Lett. 2012, 22, 7693 10.1016/j.bmcl.2012.09.104
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 7693
-
-
Fournier-Dit-Chabert, J.1
Vinader, V.2
Santos, A.R.3
Redondo-Horcajo, M.4
Dreneau, A.5
Basak, R.6
Cosentino, L.7
Marston, G.8
Abdel-Rahman, H.9
Loadman, P.M.10
Shnyder, S.D.11
Diaz, J.F.12
Barasoain, I.13
Falconer, R.A.14
Pors, K.15
-
9
-
-
0041421003
-
Combretastatin A-4 analogues as antimitotic antitumor agents
-
Nam, N. H. Combretastatin A-4 analogues as antimitotic antitumor agents Curr. Med. Chem. 2003, 10, 1697 10.2174/0929867033457151
-
(2003)
Curr. Med. Chem.
, vol.10
, pp. 1697
-
-
Nam, N.H.1
-
10
-
-
3042740981
-
BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo
-
Kuo, C. C.; Hsieh, H. P.; Pan, W. Y.; Chen, C. P.; Liou, J. P.; Lee, S. J.; Chang, Y. L.; Chen, L. T.; Chen, C. T.; Chang, J. Y. BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo Cancer Res. 2004, 64, 2004
-
(2004)
Cancer Res.
, vol.64
, pp. 2004
-
-
Kuo, C.C.1
Hsieh, H.P.2
Pan, W.Y.3
Chen, C.P.4
Liou, J.P.5
Lee, S.J.6
Chang, Y.L.7
Chen, L.T.8
Chen, C.T.9
Chang, J.Y.10
-
11
-
-
0032492959
-
Antineoplastic agents. 379. Synthesis of phenstatin phosphate
-
Pettit, G. R.; Toki, B.; Herald, D. L.; Verdier-Pinard, P.; Boyd, M. R.; Hamel, E.; Pettit, R. K. Antineoplastic agents. 379. Synthesis of phenstatin phosphate J. Med. Chem. 1998, 41, 1688 10.1021/jm970644q
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1688
-
-
Pettit, G.R.1
Toki, B.2
Herald, D.L.3
Verdier-Pinard, P.4
Boyd, M.R.5
Hamel, E.6
Pettit, R.K.7
-
12
-
-
84906094556
-
New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancer
-
La Regina, G.; Bai, R.; Coluccia, A.; Famiglini, V.; Pelliccia, S.; Passacantilli, S.; Mazzoccoli, C.; Ruggieri, V.; Sisinni, L.; Bolognesi, A.; Rensen, W. M.; Miele, A.; Nalli, M.; Alfonsi, R.; Di Marcotullio, L.; Gulino, A.; Brancale, A.; Novellino, E.; Dondio, G.; Vultaggio, S.; Varasi, M.; Mercurio, C.; Hamel, E.; Lavia, P.; Silvestri, R. New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancer J. Med. Chem. 2014, 57, 6531 10.1021/jm500561a
-
(2014)
J. Med. Chem.
, vol.57
, pp. 6531
-
-
La Regina, G.1
Bai, R.2
Coluccia, A.3
Famiglini, V.4
Pelliccia, S.5
Passacantilli, S.6
Mazzoccoli, C.7
Ruggieri, V.8
Sisinni, L.9
Bolognesi, A.10
Rensen, W.M.11
Miele, A.12
Nalli, M.13
Alfonsi, R.14
Di Marcotullio, L.15
Gulino, A.16
Brancale, A.17
Novellino, E.18
Dondio, G.19
Vultaggio, S.20
Varasi, M.21
Mercurio, C.22
Hamel, E.23
Lavia, P.24
Silvestri, R.25
more..
-
13
-
-
27744559989
-
Antiproliferative properties of piperidinylchalcones
-
Liu, X.; Go, M. L. Antiproliferative properties of piperidinylchalcones Bioorg. Med. Chem. 2006, 14, 153 10.1016/j.bmc.2005.08.006
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 153
-
-
Liu, X.1
Go, M.L.2
-
14
-
-
79952849894
-
A novel bis-indole destabilizes microtubules and displays potent in vitro and in vivo antitumor activity in prostate cancer
-
Ahn, S.; Hwang, D. J.; Barrett, C. M.; Yang, J.; Duke, C. B., 3rd; Miller, D. D.; Dalton, J. T. A novel bis-indole destabilizes microtubules and displays potent in vitro and in vivo antitumor activity in prostate cancer Cancer Chemother. Pharmacol. 2011, 67, 293 10.1007/s00280-010-1319-8
-
(2011)
Cancer Chemother. Pharmacol.
, vol.67
, pp. 293
-
-
Ahn, S.1
Hwang, D.J.2
Barrett, C.M.3
Yang, J.4
Duke, C.B.5
Miller, D.D.6
Dalton, J.T.7
-
15
-
-
78649668815
-
I-387, a novel antimitotic indole, displays a potent in vitro and in vivo antitumor activity with less neurotoxicity
-
Ahn, S.; Duke, C. B., 3rd; Barrett, C. M.; Hwang, D. J.; Li, C. M.; Miller, D. D.; Dalton, J. T. I-387, a novel antimitotic indole, displays a potent in vitro and in vivo antitumor activity with less neurotoxicity Mol. Cancer Ther. 2010, 9, 2859 10.1158/1535-7163.MCT-10-0399
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 2859
-
-
Ahn, S.1
Duke, C.B.2
Barrett, C.M.3
Hwang, D.J.4
Li, C.M.5
Miller, D.D.6
Dalton, J.T.7
-
16
-
-
77958501821
-
Discovery of novel 2-aryl-4-benzoyl-imidazoles targeting the colchicines binding site in tubulin as potential anticancer agents
-
Chen, J.; Wang, Z.; Li, C. M.; Lu, Y.; Vaddady, P. K.; Meibohm, B.; Dalton, J. T.; Miller, D. D.; Li, W. Discovery of novel 2-aryl-4-benzoyl-imidazoles targeting the colchicines binding site in tubulin as potential anticancer agents J. Med. Chem. 2010, 53, 741 10.1021/jm100884b
-
(2010)
J. Med. Chem.
, vol.53
, pp. 741
-
-
Chen, J.1
Wang, Z.2
Li, C.M.3
Lu, Y.4
Vaddady, P.K.5
Meibohm, B.6
Dalton, J.T.7
Miller, D.D.8
Li, W.9
-
17
-
-
84876841839
-
Discovery of 4-Aryl-2-benzoyl-imidazoles as tubulin polymerization inhibitor with potent antiproliferative properties
-
Xiao, M.; Ahn, S.; Wang, J.; Chen, J.; Miller, D. D.; Dalton, J. T.; Li, W. Discovery of 4-Aryl-2-benzoyl-imidazoles as tubulin polymerization inhibitor with potent antiproliferative properties J. Med. Chem. 2013, 56, 3318 10.1021/jm4001117
-
(2013)
J. Med. Chem.
, vol.56
, pp. 3318
-
-
Xiao, M.1
Ahn, S.2
Wang, J.3
Chen, J.4
Miller, D.D.5
Dalton, J.T.6
Li, W.7
-
18
-
-
79960151500
-
Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl-thiazoles analogues as potent and orally bioavailable anticancer agents
-
Lu, Y.; Li, C. M.; Wang, Z.; Chen, J.; Mohler, M. L.; Li, W.; Dalton, J. T.; Miller, D. D. Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl-thiazoles analogues as potent and orally bioavailable anticancer agents J. Med. Chem. 2011, 54, 4678 10.1021/jm2003427
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4678
-
-
Lu, Y.1
Li, C.M.2
Wang, Z.3
Chen, J.4
Mohler, M.L.5
Li, W.6
Dalton, J.T.7
Miller, D.D.8
-
19
-
-
84921448698
-
Design, synthesis, and biological evaluation of stable colchicine binding site tubulin inhibitors as potential anticancer agents
-
Lu, Y.; Chen, J.; Wang, J.; Li, C. M.; Ahn, S.; Barrett, C. M.; Dalton, J. T.; Li, W.; Miller, D. D. Design, synthesis, and biological evaluation of stable colchicine binding site tubulin inhibitors as potential anticancer agents J. Med. Chem. 2014, 57, 7355 10.1021/jm500764v
-
(2014)
J. Med. Chem.
, vol.57
, pp. 7355
-
-
Lu, Y.1
Chen, J.2
Wang, J.3
Li, C.M.4
Ahn, S.5
Barrett, C.M.6
Dalton, J.T.7
Li, W.8
Miller, D.D.9
-
20
-
-
80052351229
-
Discovery of 7-hydroxy-6-methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan (BNC105), a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties
-
Flynn, B. L.; Gill, G. S.; Grobelny, D. W.; Chaplin, J. H.; Paul, D.; Leske, A. F.; Lavranos, T. C.; Chalmers, D. K.; Charman, S. A.; Kostewicz, E.; Shackleford, D. M.; Morizzi, J.; Hamel, E.; Jung, M. K.; Kremmidiotis, G. Discovery of 7-hydroxy-6-methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan (BNC105), a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties J. Med. Chem. 2011, 54, 6014 10.1021/jm200454y
-
(2011)
J. Med. Chem.
, vol.54
, pp. 6014
-
-
Flynn, B.L.1
Gill, G.S.2
Grobelny, D.W.3
Chaplin, J.H.4
Paul, D.5
Leske, A.F.6
Lavranos, T.C.7
Chalmers, D.K.8
Charman, S.A.9
Kostewicz, E.10
Shackleford, D.M.11
Morizzi, J.12
Hamel, E.13
Jung, M.K.14
Kremmidiotis, G.15
-
21
-
-
33847172794
-
Indole, a core nucleus for potent inhibitors of tubulin polymerization
-
Brancale, A.; Silvestri, R. Indole, a core nucleus for potent inhibitors of tubulin polymerization Med. Res. Rev. 2007, 27, 209 10.1002/med.20080
-
(2007)
Med. Res. Rev.
, vol.27
, pp. 209
-
-
Brancale, A.1
Silvestri, R.2
-
22
-
-
84941574287
-
Azoles and related compounds for treatment of cancer and their preparation
-
Li, W.; Xiao, M.; Dalton, J. T.; Ahn, S.; Miller, D. D.; Chen, J.; Wang, J. Azoles and related compounds for treatment of cancer and their preparation. UTRF and GTx, 2013.
-
(2013)
UTRF and GTx
-
-
Li, W.1
Xiao, M.2
Dalton, J.T.3
Ahn, S.4
Miller, D.D.5
Chen, J.6
Wang, J.7
-
23
-
-
33744785117
-
Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase
-
Mahboobi, S.; Uecker, A.; Sellmer, A.; Cenac, C.; Hocher, H.; Pongratz, H.; Eichhorn, E.; Hufsky, H.; Trumpler, A.; Sicker, M.; Heidel, F.; Fischer, T.; Stocking, C.; Elz, S.; Bohmer, F. D.; Dove, S. Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase J. Med. Chem. 2006, 49, 3101 10.1021/jm058033i
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3101
-
-
Mahboobi, S.1
Uecker, A.2
Sellmer, A.3
Cenac, C.4
Hocher, H.5
Pongratz, H.6
Eichhorn, E.7
Hufsky, H.8
Trumpler, A.9
Sicker, M.10
Heidel, F.11
Fischer, T.12
Stocking, C.13
Elz, S.14
Bohmer, F.D.15
Dove, S.16
-
24
-
-
84860312887
-
Synthesis and biological evaluation of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo
-
Lai, M. J.; Huang, H. L.; Pan, S. L.; Liu, Y. M.; Peng, C. Y.; Lee, H. Y.; Yeh, T. K.; Huang, P. H.; Teng, C. M.; Chen, C. S.; Chuang, H. Y.; Liou, J. P. Synthesis and biological evaluation of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo J. Med. Chem. 2012, 55, 3777 10.1021/jm300197a
-
(2012)
J. Med. Chem.
, vol.55
, pp. 3777
-
-
Lai, M.J.1
Huang, H.L.2
Pan, S.L.3
Liu, Y.M.4
Peng, C.Y.5
Lee, H.Y.6
Yeh, T.K.7
Huang, P.H.8
Teng, C.M.9
Chen, C.S.10
Chuang, H.Y.11
Liou, J.P.12
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