-
1
-
-
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. (Pubitemid 38525281)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
2
-
-
77957374075
-
Microtubule-binding agents: A dynamic field of cancer therapeutics
-
C. Dumontet, M.A. Jordan, Microtubule-binding agents: a dynamic field of cancer therapeutics, Nat. Rev. Drug Discov. 9 (2010) 790-803.
-
(2010)
Nat. Rev. Drug Discov.
, vol.9
, pp. 790-803
-
-
Dumontet, C.1
Jordan, M.A.2
-
3
-
-
33750701126
-
Drug target interaction of tubulin-binding drugs in cancer therapy
-
DOI 10.1586/14737140.6.10.1433
-
S. Sengupta, S.A. Thomas, Drug target interaction of tubulin-binding drugs in cancer therapy, Expert Rev. Anticancer Ther. 6 (2006) 1433-1447. (Pubitemid 44697168)
-
(2006)
Expert Review of Anticancer Therapy
, vol.6
, Issue.10
, pp. 1433-1447
-
-
Sengupta, S.1
Thomas, S.A.2
-
4
-
-
78649833819
-
The unique characteristics of tumor vasculature and preclinical evidence for its selective disruption by tumor-vascular disrupting agents
-
D.W. Siemann, The unique characteristics of tumor vasculature and preclinical evidence for its selective disruption by tumor-vascular disrupting agents, Cancer Treat. Rev. 37 (2011) 63-74.
-
(2011)
Cancer Treat. Rev.
, vol.37
, pp. 63-74
-
-
Siemann, D.W.1
-
5
-
-
79953741443
-
A perspective on vascular disrupting agents that interact with tubulin: Preclinical tumor imaging and biological assessment
-
R.P. Mason, D. Zhao, L. Liu, L. Trawick, K.G. Pinney, A perspective on vascular disrupting agents that interact with tubulin: preclinical tumor imaging and biological assessment, Integr. Biol. 3 (2011) 375-387.
-
(2011)
Integr. Biol.
, vol.3
, pp. 375-387
-
-
Mason, R.P.1
Zhao, D.2
Liu, L.3
Trawick, L.4
Pinney, K.G.5
-
6
-
-
84866347315
-
Design and synthesis of diarylamines and diarylethers as cytotoxic antitumor agents
-
X.F. Wang, X.T. Tian, E. Ohkoshi, B.J. Qin, Y.N. Liu, P.C. Wu, H.Y. Hung, M.J. Hour, K. Qian, R. Huang, K.F. Bastow, W.P. Janzen, J. Jin, S.L. Morris- Natschke, K.H. Lee, L. Xie, Design and synthesis of diarylamines and diarylethers as cytotoxic antitumor agents, Bioorg. Med. Chem. Lett. 22 (2012) 6224-6228.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 6224-6228
-
-
Wang, X.F.1
Tian, X.T.2
Ohkoshi, E.3
Qin, B.J.4
Liu, Y.N.5
Wu, P.C.6
Hung, H.Y.7
Hour, M.J.8
Qian, K.9
Huang, R.10
Bastow, K.F.11
Janzen, W.P.12
Jin, J.13
Morris- Natschke, S.L.14
Lee, K.H.15
Xie, L.16
-
7
-
-
84872303107
-
Synthesis and biological evaluation of N-alkyl-N-(4-methoxyphenyl) pyridin-2-amines as a new class of tubulin polymerization inhibitors
-
X.F. Wang, E. Ohkoshi, S.B. Wang, E. Hamel, K.F. Bastow, S.L. Morris-Natschke, K.H. Lee, L. Xie, Synthesis and biological evaluation of N-alkyl-N-(4-methoxyphenyl)pyridin-2-amines as a new class of tubulin polymerization inhibitors, Bioorg. Med. Chem. 21 (2013) 632-642.
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 632-642
-
-
Wang, X.F.1
Ohkoshi, E.2
Wang, S.B.3
Hamel, E.4
Bastow, K.F.5
Morris-Natschke, S.L.6
Lee, K.H.7
Xie, L.8
-
8
-
-
33846363963
-
Structure eactivity relationships for in vitro and in vivo toxicity
-
W. Anthony (Ed.), Academic Press
-
J. Blagg, Structure eactivity relationships for in vitro and in vivo toxicity, in: W. Anthony (Ed.), Annual Reports in Medicinal Chemistry, vol. 41, Academic Press, 2006, pp. 353-368.
-
(2006)
Annual Reports in Medicinal Chemistry
, vol.41
, pp. 353-368
-
-
Blagg, J.1
-
9
-
-
45949086656
-
Metabolic stability
-
Academic Press, San Diego
-
E.H. Kerns, L. Di, Metabolic stability, in: In Drug-like Properties: Concepts, Structure Design and Methods, Academic Press, San Diego, 2008, p. 151.
-
(2008)
Drug-like Properties: Concepts, Structure Design and Methods
, pp. 151
-
-
Kerns, E.H.1
Di, L.2
-
10
-
-
31144479417
-
Regioselective copper-catalyzed amination of chlorobenzoic acids: Synthesis and solid-state structures of N-aryl anthranilic acid derivatives
-
DOI 10.1021/jo0518809
-
X. Mei, A.T. August, C. Wolf, Regioselective copper-catalyzed amination of chlorobenzoic acids: synthesis and solid-state structures of N-aryl anthranilic acid derivatives, J. Org. Chem. 71 (2006) 142-149. (Pubitemid 43128070)
-
(2006)
Journal of Organic Chemistry
, vol.71
, Issue.1
, pp. 142-149
-
-
Mei, X.1
August, A.T.2
Wolf, C.3
-
11
-
-
3543046740
-
Rapid and efficient microwave-assisted synthesis of aryl aminobenzophenones using Pd-catalyzed amination
-
DOI 10.1021/jo049572i
-
T.A. Jensen, X. Liang, D. Tanner, N. Skjaerbaek, Rapid and efficient microwaveassisted synthesis of aryl aminobenzophenones using Pd-catalyzed amination, J. Org. Chem. 69 (2004) 4936-4947. (Pubitemid 39014048)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.15
, pp. 4936-4947
-
-
Jensen, T.A.1
Liang, X.2
Tanner, D.3
Skjaerbaek, N.4
-
12
-
-
40749153864
-
Synthesis and evaluation of antitumoral activity of ester and amide derivatives of 2-arylamino-6-trifluoromethyl-3-pyridinecarboxylic acids
-
DOI 10.1016/j.bmc.2007.11.069, PII S0968089607010371
-
V. Onnis, M.T. Cocco, V. Lilliu, C. Congiu, Synthesis and evaluation of antitumor activity of ester and amide derivatives of 2-arylamino-6- trifluoromethyl-3-pyridinecarboxylic acids, Bioorg. Med. Chem. 16 (2008) 2367-2378. (Pubitemid 351380946)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.5
, pp. 2367-2378
-
-
Onnis, V.1
Cocco, M.T.2
Lilliu, V.3
Congiu, C.4
-
13
-
-
85008072114
-
Reduction of heterocyclic compounds. II. Reduction of heterocyclic compounds with sodium borohydride-transition metal salt systems
-
A. Nose, T. Kudo, Reduction of heterocyclic compounds. II. Reduction of heterocyclic compounds with sodium borohydride-transition metal salt systems, Chem. Pharm. Bull. 32 (1984) 2421-2425.
-
(1984)
Chem. Pharm. Bull.
, vol.32
, pp. 2421-2425
-
-
Nose, A.1
Kudo, T.2
-
14
-
-
77954034124
-
Multidrug resistance in oral squamous cell carcinoma: The role of vacuolar ATPases
-
M. Perez-Sayans, J.M. Somoza-Martin, F. Barros-Angueira, P.G. Diz, J.M. Rey, A. Garcia-Garcia, Multidrug resistance in oral squamous cell carcinoma: the role of vacuolar ATPases, Cancer Lett. 295 (2010) 135-143.
-
(2010)
Cancer Lett.
, vol.295
, pp. 135-143
-
-
Perez-Sayans, M.1
Somoza-Martin, J.M.2
Barros-Angueira, F.3
Diz, P.G.4
Rey, J.M.5
Garcia-Garcia, A.6
-
15
-
-
84862285321
-
Antitumor agents. 293. Nontoxic dimethyl-4,4′-dimethoxy-5,6, 5′,6′-dime-thylenedioxylbiphenyl-2,2′-dicarboxylate (DDB) analogues chemosensitize multidrug-resistant cancer cells to clinical anticancer drugs
-
H.Y. Hung, E. Ohkoshi, M. Goto, K.F. Bastow, K. Nakagawa-Goto, K.H. Lee, Antitumor agents. 293. Nontoxic dimethyl-4,4′-dimethoxy-5,6,5′, 6′-dime-thylenedioxylbiphenyl-2,2′-dicarboxylate (DDB) analogues chemosensitize multidrug-resistant cancer cells to clinical anticancer drugs, J. Med. Chem. 55 (2012) 5413-5424.
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5413-5424
-
-
Hung, H.Y.1
Ohkoshi, E.2
Goto, M.3
Bastow, K.F.4
Nakagawa-Goto, K.5
Lee, K.H.6
-
16
-
-
0025367455
-
Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines
-
L.V. Rubinstein, R.H. Shoemaker, R.M. Paull, S. Tosini, P. Skehan, D.A. Scudiero, A. Monks, M.R. Boyd, Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines, J. Natl. Cancer Inst. 82 (1990) 1113-1117.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1113-1117
-
-
Rubinstein, L.V.1
Shoemaker, R.H.2
Paull, R.M.3
Tosini, S.4
Skehan, P.5
Scudiero, D.A.6
Monks, A.7
Boyd, M.R.8
-
17
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
R.B.G. Ravelli, B. Gigant, P.A. Curmi, I. Jourdain, S. Lachkar, A. Sobel, M. Knossow, Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain, Nature 428 (2004) 198e202.
-
(2004)
Nature
, vol.428
-
-
Ravelli, R.B.G.1
Gigant, B.2
Curmi, P.A.3
Jourdain, I.4
Lachkar, S.5
Sobel, A.6
Knossow, M.7
-
18
-
-
69549122767
-
Variations in the colchicine-binding domain provide insight into the structural switch of tubulin
-
A. Dorleans, B. Gigant, R.B.G. Ravelli, P. Mailliet, V. Mikol, M. Knossow, Variations in the colchicine-binding domain provide insight into the structural switch of tubulin, Proc. Natl. Acad. Sci. U. S. A. 106 (2009) 13775-13779.
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 13775-13779
-
-
Dorleans, A.1
Gigant, B.2
Ravelli, R.B.G.3
Mailliet, P.4
Mikol, V.5
Knossow, M.6
-
19
-
-
78649509037
-
Synthesis and discovery of water-soluble microtubule targeting agents that binding to the colchicine site on tubulin and circumvent Pgp medicated resistance
-
A. Gangjee, Y. Zhao, L. Lin, S. Raghavan, E.G. Roberts, A.L. Risinger, E. Hamel, S.L. Mooberry, Synthesis and discovery of water-soluble microtubule targeting agents that binding to the colchicine site on tubulin and circumvent Pgp medicated resistance, J. Med. Chem. 53 (2010) 8116-8128.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8116-8128
-
-
Gangjee, A.1
Zhao, Y.2
Lin, L.3
Raghavan, S.4
Roberts, E.G.5
Risinger, A.L.6
Hamel, E.7
Mooberry, S.L.8
-
20
-
-
84866918553
-
Design, synthesis, and preclinical evaluations of novel 4-substituted 1,5-diarylanilines as potent HIV-1 non-nucleoside reverse transcriptase inhibitor (NNRTI) drug candidates
-
L.Q. Sun, L. Zhu, K. Qian, B. Qin, L. Huang, C.H. Chen, K.H. Lee, L. Xie, Design, synthesis, and preclinical evaluations of novel 4-substituted 1,5-diarylanilines as potent HIV-1 non-nucleoside reverse transcriptase inhibitor (NNRTI) drug candidates, J. Med. Chem. 55 (2012) 7219-7229.
-
(2012)
J. Med. Chem.
, vol.55
, pp. 7219-7229
-
-
Sun, L.Q.1
Zhu, L.2
Qian, K.3
Qin, B.4
Huang, L.5
Chen, C.H.6
Lee, K.H.7
Xie, L.8
-
21
-
-
34248159068
-
Small molecule vascular disrupting agents: Potential new drugs for cancer treatment
-
S.X. Cai, Small molecule vascular disrupting agents: potential new drugs for cancer treatment, Anti-Cancer Drugs 2 (2007) 79-101. (Pubitemid 46723154)
-
(2007)
Recent Patents on Anti-Cancer Drug Discovery
, vol.2
, Issue.1
, pp. 79-101
-
-
Cai, S.X.1
-
22
-
-
0000719887
-
Status of the NCI preclinical antitumor drug discovery screen
-
V.T. Devita, S. Hellman, S.A. Rosenberg (Eds.), J. B. Lippincott, Philadelphia
-
M.R. Boyd, Status of the NCI preclinical antitumor drug discovery screen, in: V.T. Devita, S. Hellman, S.A. Rosenberg (Eds.), Cancer: Principles and Practice of Oncology Updates, J. B. Lippincott, Philadelphia, 1989, pp. 1-12.
-
(1989)
Cancer: Principles and Practice of Oncology Updates
, pp. 1-12
-
-
Boyd, M.R.1
-
23
-
-
0025775062
-
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
-
A. Monks, D. Scudiero, P. Skehan, R. Shoemaker, K. Paull, D. Vistica, C. Hose, J. Langley, P. Cronise, A. Vaigro-Woiff, M. Gray-Goodrich, H. Campbell, J. Mayo, M. Boyd, Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines, J. Natl. Cancer Inst. 83 (1991) 757-766.
-
(1991)
J. Natl. Cancer Inst.
, vol.83
, pp. 757-766
-
-
Monks, A.1
Scudiero, D.2
Skehan, P.3
Shoemaker, R.4
Paull, K.5
Vistica, D.6
Hose, C.7
Langley, J.8
Cronise, P.9
Vaigro-Woiff, A.10
Gray-Goodrich, M.11
Campbell, H.12
Mayo, J.13
Boyd, M.14
-
24
-
-
34249850360
-
The sulphorhodamine (SRB) assay and other approaches to testing plant extracts and derived compounds for activities related to reputed anticancer activity
-
DOI 10.1016/j.ymeth.2007.01.003, PII S1046202307000060, Natural Product Research: The Challenges Facing the Modern Researcher
-
P. Houghton, R. Fang, I. Techatanawat, G. Steventon, P.J. Hylands, C.C. Lee, The sulphorhodamine (SRB) assay and other approaches to testing plant extracts and derived compounds for activities related to reputed anticancer activity, Methods 42 (2007) 377-387. (Pubitemid 46860387)
-
(2007)
Methods
, vol.42
, Issue.4
, pp. 377-387
-
-
Houghton, P.1
Fang, R.2
Techatanawat, I.3
Steventon, G.4
Hylands, P.J.5
Lee, C.C.6
-
25
-
-
0142036683
-
Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin
-
E. Hamel, Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin, Cell Biochem. Biophys. 38 (2003) 1-22.
-
(2003)
Cell Biochem. Biophys.
, vol.38
, pp. 1-22
-
-
Hamel, E.1
-
26
-
-
0024427745
-
Antimitotic natural products combretastatin A-4 and combretastatin A-2: Studies on the mechanism of their inhibition of the binding of colchicine to tubulin
-
C.M. Lin, H.H. Ho, G.R. Pettit, E. Hamel, Antimitotic natural products combretastatin A-4 and combretastatin A-2: studies on the mechanism of their inhibition of the binding of colchicine to tubulin, Biochemistry 28 (1989) 6984-6991. (Pubitemid 19219888)
-
(1989)
Biochemistry
, vol.28
, Issue.17
, pp. 6984-6991
-
-
Lin, C.M.1
Ho, H.H.2
Pettit, G.R.3
Hamel, E.4
|