-
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, 253-265 (Pubitemid 38525281)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
2
-
-
77958058948
-
Microtubule Dynamics
-
Begley, T. P. et al. John Wiley and Sons, Inc. Hoboken, NJ
-
Lopus, M.; Yenjerle, M.; Wilson, L. Microtubule Dynamics. In Wiley Encyclopedia of Chemical Biology; Begley, T. P., et al.; Eds.; John Wiley and Sons, Inc.: Hoboken, NJ, 2008; 3, 153-160.
-
(2008)
Wiley Encyclopedia of Chemical Biology
, vol.3
, pp. 153-160
-
-
Lopus, M.1
Yenjerle, M.2
Wilson, L.3
-
3
-
-
75749155892
-
From signaling pathways to microtubule dynamics: The key players
-
Etienne-Manneville, S. From signaling pathways to microtubule dynamics: the key players Curr. Opin. Cell Biol. 2010, 22, 104-111
-
(2010)
Curr. Opin. Cell Biol.
, vol.22
, pp. 104-111
-
-
Etienne-Manneville, S.1
-
4
-
-
70350571135
-
On and around microtubules: An overview
-
Wade, R. H. On and around microtubules: an overview Mol. Biotechnol. 2009, 43, 177-191
-
(2009)
Mol. Biotechnol.
, vol.43
, pp. 177-191
-
-
Wade, R.H.1
-
5
-
-
0035744348
-
Anticancer therapy with novel tubulin-interacting drugs
-
DOI 10.1054/drup.2002.0230
-
Kavallaris, M.; Verrills, N. M.; Hill, B. T. Anticancer therapy with novel tubulin-interacting drugs Drug Resist. Updates 2001, 4, 392-401 (Pubitemid 34746873)
-
(2001)
Drug Resistance Updates
, vol.4
, Issue.6
, pp. 392-401
-
-
Kavallaris, M.1
Verrills, N.M.2
Hill, B.T.3
-
6
-
-
84906431645
-
-
Hearn, B. R.; Shaw, S. J.; Myles, D. C. Microtubule Targeting Agents, Compr. Med. Chem. II 2006, 7, 81-110
-
(2006)
Microtubule Targeting Agents, Compr. Med. Chem. II
, vol.7
, pp. 81-110
-
-
Hearn, B.R.1
Shaw, S.J.2
Myles, D.C.3
-
7
-
-
76849087811
-
Taxanes: Optimizing adjuvant chemotherapy for early-stage breast cancer
-
Bedard, P. L.; Di Leo, A.; Piccart-Gebhart, M. J. Taxanes: optimizing adjuvant chemotherapy for early-stage breast cancer Nat. Rev. Clin. Oncol 2010, 7, 22-36
-
(2010)
Nat. Rev. Clin. Oncol
, vol.7
, pp. 22-36
-
-
Bedard, P.L.1
Di Leo, A.2
Piccart-Gebhart, M.J.3
-
8
-
-
0141774441
-
Tubulin and microtubules as targets for anticancer drugs
-
Hadfield, J. A.; Ducki, S.; Hirst, N.; McGown, A. T. Tubulin and microtubules as targets for anticancer drugs Prog. Cell Cycle Res. 2003, 5, 309-325
-
(2003)
Prog. Cell Cycle Res.
, vol.5
, pp. 309-325
-
-
Hadfield, J.A.1
Ducki, S.2
Hirst, N.3
McGown, A.T.4
-
9
-
-
70450230732
-
Recent developments and SAR analysis of colchicine binding site inhibitors
-
Chen, J.; Liu., T.; Dong, X.; Hu, Y. Recent developments and SAR analysis of colchicine binding site inhibitors Mini-Rev. Med. Chem. 2009, 9, 1174-1190
-
(2009)
Mini-Rev. Med. Chem.
, vol.9
, pp. 1174-1190
-
-
Chen, J.1
Liu, T.2
Dong, X.3
Hu, Y.4
-
10
-
-
37349083149
-
Combretastatin A-4 analogs as anticancer agents
-
DOI 10.2174/138955707782795647
-
Chaudhary, A.; Pandeya, S. N.; Kumar, P.; Sharma, P. P.; Gupta, S.; Soni, N.; Verma, K. K.; Bhardwaj, G. Combretastatin A-4 analogs as anticancer agents Mini-Rev. Med. Chem. 2007, 7, 1186-1205 (Pubitemid 350303084)
-
(2007)
Mini-Reviews in Medicinal Chemistry
, vol.7
, Issue.12
, pp. 1186-1205
-
-
Chaudhary, A.1
Pandeya, S.N.2
Kumar, P.3
Sharma, P.P.4
Gupta, S.5
Soni, N.6
Verma, K.K.7
Bhardwaj, G.8
-
11
-
-
33744820579
-
Medicinal chemistry of combretastatin A4: Present and future directions
-
DOI 10.1021/jm0512903
-
Tron, G. C.; Pirali, T.; Sorba, G.; Pagliai, F.; Busacca, S.; Genazzani, A. A. Medicinal chemistry of combretastatin A4: present and future directions J. Med. Chem. 2006, 49, 3033-3044 (Pubitemid 43830499)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.11
, pp. 3033-3044
-
-
Tron, G.C.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
12
-
-
85008389252
-
The Discovery and Development of the Combretastatins
-
Cragg, G. M. Kingston, D. G. I. Newman, D. J. Eds; Taylor and Francis: Boca Raton, FL
-
Pinney, K. G.; Jelinek, C.; Edvardsen, K.; Chaplin, D. J.; Pettit, G. R. The Discovery and Development of the Combretastatins. In Anticancer Agents from Natural Products; Cragg, G. M.; Kingston, D. G. I.; Newman, D. J., Eds; Taylor and Francis: Boca Raton, FL, 2005; pp 23-46.
-
(2005)
Anticancer Agents from Natural Products
, pp. 23-46
-
-
Pinney, K.G.1
Jelinek, C.2
Edvardsen, K.3
Chaplin, D.J.4
Pettit, G.R.5
-
13
-
-
37249020371
-
Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin
-
DOI 10.1002/med.20097
-
Bhattacharyya, B.; Panda, D.; Gupta, S.; Banerjee, M. Antimitotic activity of colchicine and the structural basis for its interaction with tubulin Med. Res. Rev. 2008, 28, 155-183 (Pubitemid 350274963)
-
(2008)
Medicinal Research Reviews
, vol.28
, Issue.1
, pp. 155-183
-
-
Bhattacharyya, B.1
Panda, D.2
Gupta, S.3
Banerjee, M.4
-
14
-
-
78649502493
-
An Overview of Compounds That Interact with Tubulin and Their Effects on Microtubule Assembly
-
Fojo, T. Humana Press: Totowa, NJ
-
Hamel, E. An Overview of Compounds That Interact with Tubulin and Their Effects on Microtubule Assembly. In The Role of Microtubules in Cell Biology, Neurobiology and Oncology; Fojo, T., Ed.; Humana Press: Totowa, NJ, 2008; pp 1-19.
-
(2008)
The Role of Microtubules in Cell Biology, Neurobiology and Oncology
, pp. 1-19
-
-
Hamel, E.1
-
15
-
-
77955319048
-
Substituted 2-(3′,4′,5′-trimethoxybenzoyl)-benzo[ b ]thiophene derivatives as potent tubulin polymerization inhibitors
-
Romagnoli, R.; Baraldi, P. G.; Carrion, M. D.; Cruz-Lopez, O.; Tolomeo, M.; Grimaudo, S.; Di Cristina, A.; Pipitone, M. R.; Balzarini, J.; Brancale, A.; Hamel, E. Substituted 2-(3′,4′,5′-trimethoxybenzoyl)-benzo[ b ]thiophene derivatives as potent tubulin polymerization inhibitors Bioorg. Med. Chem. 2010, 18, 5114-5122
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 5114-5122
-
-
Romagnoli, R.1
Baraldi, P.G.2
Carrion, M.D.3
Cruz-Lopez, O.4
Tolomeo, M.5
Grimaudo, S.6
Di Cristina, A.7
Pipitone, M.R.8
Balzarini, J.9
Brancale, A.10
Hamel, E.11
-
16
-
-
44149102682
-
Synthesis and antiproliferative activity of imidazole and imidazoline analogs for melanoma
-
DOI 10.1016/j.bmcl.2008.04.073, PII S0960894X08004770
-
Chen, J.; Wang, Z.; Lu, Y.; Dalton, J. T.; Miller, D. D.; Li, W. Synthesis and antiproliferative activity of imidazole and imidazoline analogs for melanoma Bioorg. Med. Chem. Lett. 2008, 18, 3183-3187 (Pubitemid 351718344)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.11
, pp. 3183-3187
-
-
Chen, J.1
Wang, Z.2
Lu, Y.3
Dalton, J.T.4
Miller, D.D.5
Li, W.6
-
17
-
-
64349111929
-
Discovery of 4-substituted methoxybenzoyl-aryl-thiazoles as novel anticancer agents: Synthesis, biological evaluation, and structure-activity relationships
-
Lu, Y.; Li, C. M.; Wang, Z.; Ross, C. R., II; Chen, J.; Dalton, J. T.; Li, W.; Miller, D. D. Discovery of 4-substituted methoxybenzoyl-aryl-thiazoles as novel anticancer agents: synthesis, biological evaluation, and structure-activity relationships J. Med. Chem. 2009, 52, 1701-1711
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1701-1711
-
-
Lu, Y.1
Li, C.M.2
Wang, Z.3
Ross, C.R.I.I.4
Chen, J.5
Dalton, J.T.6
Li, W.7
Miller, D.D.8
-
18
-
-
72249084715
-
New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis, tubulin polymerization, cell growth inhibition, and molecular modeling studies
-
La Regina, G.; Sarkar, T.; Bai, R.; Edler, M. C.; Saletti, R.; Coluccia, A.; Piscitelli, F.; Minelli, L.; Gatti, V.; Mazzoccoli, C.; Palermo, V.; Mazzoni, C.; Falcone, C.; Scovassi, A. I.; Giansanti, V.; Campiglia, P.; Porta, A.; Maresca, B.; Hamel, E.; Brancale, A.; Novellino, E.; Silvestri, R. New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis, tubulin polymerization, cell growth inhibition, and molecular modeling studies J. Med. Chem. 2009, 52, 7512-7527
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7512-7527
-
-
La Regina, G.1
Sarkar, T.2
Bai, R.3
Edler, M.C.4
Saletti, R.5
Coluccia, A.6
Piscitelli, F.7
Minelli, L.8
Gatti, V.9
Mazzoccoli, C.10
Palermo, V.11
Mazzoni, C.12
Falcone, C.13
Scovassi, A.I.14
Giansanti, V.15
Campiglia, P.16
Porta, A.17
Maresca, B.18
Hamel, E.19
Brancale, A.20
Novellino, E.21
Silvestri, R.22
more..
-
19
-
-
78649509037
-
Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance
-
Gangjee, A.; Zhao, T.; Lin, L.; Raghavan, S.; Roberts, E. G.; Risinger, A. L.; Hamel, E.; Mooberry, S. L. Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance J. Med. Chem. 2010, 53, 8116-8128
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8116-8128
-
-
Gangjee, A.1
Zhao, T.2
Lin, L.3
Raghavan, S.4
Roberts, E.G.5
Risinger, A.L.6
Hamel, E.7
Mooberry, S.L.8
-
20
-
-
77956765452
-
4-(3-Halo/amino-4,5-dimethoxyphenyl)-5-aryloxazoles and - N -methylimidazoles that are cytotoxic against combretastatin A-4 resistant tumor cells and vascular disrupting in a cisplatin resistant germ cell tumor model
-
Schobert, R.; Biersack, B.; Dietrich, A.; Effenberger, K.; Knauer, S.; Mueller, T. 4-(3-Halo/amino-4,5-dimethoxyphenyl)-5-aryloxazoles and-N -methylimidazoles that are cytotoxic against combretastatin A-4 resistant tumor cells and vascular disrupting in a cisplatin resistant germ cell tumor model J. Med. Chem. 2010, 53, 6595-6602
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6595-6602
-
-
Schobert, R.1
Biersack, B.2
Dietrich, A.3
Effenberger, K.4
Knauer, S.5
Mueller, T.6
-
21
-
-
77956298509
-
Identification of CKD-516: A potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors
-
Lee, J.; Kim, S. J.; Choi, H.; Kim, Y. H.; Lim, I. T.; Yang, H.-M.; Lee, C. S.; Kang, H. R.; Ahn, S. K.; Moon, S. K.; Kim, D.-H.; Lee, S.; Choi, N. M.; Lee, K. J. Identification of CKD-516: a potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors J. Med. Chem. 2010, 53, 6337-6354
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6337-6354
-
-
Lee, J.1
Kim, S.J.2
Choi, H.3
Kim, Y.H.4
Lim, I.T.5
Yang, H.-M.6
Lee, C.S.7
Kang, H.R.8
Ahn, S.K.9
Moon, S.K.10
Kim, D.-H.11
Lee, S.12
Choi, N.M.13
Lee, K.J.14
-
22
-
-
77952737457
-
Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cis-restricted combretastatin analogues
-
Romagnoli, R.; Baraldi, P. G.; Cruz-Lopez, O.; Cara, C. L.; Carrion, M. D.; Brancale, A.; Hamel, E.; Chen, L.; Bortolozzi, R.; Basso, G.; Viola, G. Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cis-restricted combretastatin analogues J. Med. Chem. 2010, 53, 4248-4258
-
(2010)
J. Med. Chem.
, vol.53
, pp. 4248-4258
-
-
Romagnoli, R.1
Baraldi, P.G.2
Cruz-Lopez, O.3
Cara, C.L.4
Carrion, M.D.5
Brancale, A.6
Hamel, E.7
Chen, L.8
Bortolozzi, R.9
Basso, G.10
Viola, G.11
-
23
-
-
77950564911
-
Synthesis, antitubulin, and antiproliferative SAR of analogues of 2-methoxyestradiol-3,17- O, O -bis-sulfamate
-
Jourdan, F.; Leese, M. P.; Dohle, W.; Hamel, E.; Ferrandis, E.; Newman, S. P.; Purohit, A.; Reed, M. J.; Potter, B. V. L. Synthesis, antitubulin, and antiproliferative SAR of analogues of 2-methoxyestradiol-3,17- O, O -bis-sulfamate J. Med. Chem. 2010, 53, 2942-2951
-
(2010)
J. Med. Chem.
, vol.53
, pp. 2942-2951
-
-
Jourdan, F.1
Leese, M.P.2
Dohle, W.3
Hamel, E.4
Ferrandis, E.5
Newman, S.P.6
Purohit, A.7
Reed, M.J.8
Potter, B.V.L.9
-
24
-
-
74849140125
-
Design, synthesis, and biological evaluations of 2,5-diaryl-2,3-dihydro- 1,3,4-oxadiazoline analogs of combretastatin-A4
-
Lee, L.; Robb, L. M.; Lee, M.; Davis, R.; Mackay, H.; Chavda, S.; Babu, B.; L.; O'Brien, E.; Risinger, A. L.; Mooberry, S. L.; Lee, M. Design, synthesis, and biological evaluations of 2,5-diaryl-2,3-dihydro-1,3,4- oxadiazoline analogs of combretastatin-A4 J. Med. Chem. 2010, 53, 325-334
-
(2010)
J. Med. Chem.
, vol.53
, pp. 325-334
-
-
Lee, L.1
Robb, L.M.2
Lee, M.3
Davis, R.4
MacKay, H.5
Chavda, S.6
Babu, B.L.7
O'brien, E.8
Risinger, A.L.9
Mooberry, S.L.10
Lee, M.11
-
25
-
-
72249107517
-
Vascular disrupting activity of tubulin-binding 1,5-diaryl-1 H -imidazoles
-
Bonezzi, K.; Taraboletti, G.; Borsotti, P.; Bellina, F.; Rossi, R.; Giavazz, R. Vascular disrupting activity of tubulin-binding 1,5-diaryl-1 H -imidazoles J. Med. Chem. 2009, 52, 7906-7910
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7906-7910
-
-
Bonezzi, K.1
Taraboletti, G.2
Borsotti, P.3
Bellina, F.4
Rossi, R.5
Giavazz, R.6
-
26
-
-
68549135156
-
Synthesis and evaluation of 3-aroylindoles as anticancer agents: Metabolite approach
-
Wu, Y.-S.; Coumar, M. S.; Chang, J.-Y.; Sun, H.-Y.; Kuo, F.-M.; Kuo, C.-C.; C., Y.-J.; Chang, C.-Y.; Hsiao, C.-L.; Liou, J.-P.; Chen, C.-P.; Yao, H.-T.; Chiang, Y.-K.; Tan, U.-K.; Chen, C.-T.; Chu, C.-Y.; Wu, S.-Y.; Yeh, T.-K.; Lin, C.-Y.; Hsieh, H.-P. Synthesis and evaluation of 3-aroylindoles as anticancer agents: metabolite approach J. Med. Chem. 2009, 52, 4941-4945
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4941-4945
-
-
Wu, Y.-S.1
Coumar, M.S.2
Chang, J.-Y.3
Sun, H.-Y.4
Kuo, F.-M.5
Kuo, C.-C.6
Chang, C.-Y.7
Hsiao, C.-L.8
Liou, J.-P.9
Chen, C.-P.10
Yao, H.-T.11
Chiang, Y.-K.12
Tan, U.-K.13
Chen, C.-T.14
Chu, C.-Y.15
Wu, S.-Y.16
Yeh, T.-K.17
Lin, C.-Y.18
Hsieh, H.-P.19
-
27
-
-
48449088613
-
-
Ty, N.; Dupeyre, G.; Chabot, G. G.; Seguin, J.; Tillequin, F.; Scherman, D.; Michel, S.; Cahcet, X. Bioorg. Med. Chem. 2008, 16, 7494-7503
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 7494-7503
-
-
Ty, N.1
Dupeyre, G.2
Chabot, G.G.3
Seguin, J.4
Tillequin, F.5
Scherman, D.6
Michel, S.7
Cahcet, X.8
-
28
-
-
67650720900
-
Generation of ligand-based pharmacophore model and virtual screening for identification of novel tubulin inhibitors with potent anticancer activity
-
Chiang, Y.-K.; Kuo, C.-C.; Wu, Y.-S.; Chen, C.-T.; Coumar, M. S.; Wu, J.-S.; Hsieh, H.-P.; Chang, C.-Y.; Jseng, H.-Y.; Wu, M.-H.; Leou, J.-S.; Song, J.-S.; Chang, J.-Y.; Lyu, P.-C.; Chao, Y.-S.; Wu, S.-Y. Generation of ligand-based pharmacophore model and virtual screening for identification of novel tubulin inhibitors with potent anticancer activity J. Med. Chem. 2009, 52, 4221-4233
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4221-4233
-
-
Chiang, Y.-K.1
Kuo, C.-C.2
Wu, Y.-S.3
Chen, C.-T.4
Coumar, M.S.5
Wu, J.-S.6
Hsieh, H.-P.7
Chang, C.-Y.8
Jseng, H.-Y.9
Wu, M.-H.10
Leou, J.-S.11
Song, J.-S.12
Chang, J.-Y.13
Lyu, P.-C.14
Chao, Y.-S.15
Wu, S.-Y.16
-
29
-
-
0036075878
-
Small-molecule, tubulin-binding compounds as vascular targeting agents
-
Max, M. A. Small-molecule, tubulin-binding compounds as vascular targeting agents Expert Opin. Ther. Pat. 2002, 12, 769-776
-
(2002)
Expert Opin. Ther. Pat.
, vol.12
, pp. 769-776
-
-
Max, M.A.1
-
30
-
-
20344379950
-
Disrupting tumour blood vessels
-
DOI 10.1038/nrc1628
-
Tozer, G. M.; Kanthou, C.; Baguley, B. C. Disrupting tumour blood vessels Nat. Rev. Cancer 2005, 5, 423-435 (Pubitemid 40791485)
-
(2005)
Nature Reviews Cancer
, vol.5
, Issue.6
, pp. 423-435
-
-
Tozer, G.M.1
Kanthou, C.2
Baguley, B.C.3
-
31
-
-
2642571660
-
Vascular-targeting therapies for treatment of malignant disease
-
DOI 10.1002/cncr.20299
-
Siemann, D. W.; Chaplin, D. J.; Horsman, M. R. Vascular targeted therapies for treatment of malignant disease Cancer 2004, 100, 2491-2499 (Pubitemid 38715753)
-
(2004)
Cancer
, vol.100
, Issue.12
, pp. 2491-2499
-
-
Siemann, D.W.1
Chaplin, D.J.2
Horsman, M.R.3
-
32
-
-
0037085753
-
The tumor vascular targeting agent combretastatin A-4-phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells
-
DOI 10.1182/blood.V99.6.2060
-
Kanthou, C.; Tozer, G. M. The tumor vascular targeting agent combretastatin A-4 phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells Blood 2002, 99, 2060-2069 (Pubitemid 34525489)
-
(2002)
Blood
, vol.99
, Issue.6
, pp. 2060-2069
-
-
Kanthou, C.1
Tozer, G.M.2
-
33
-
-
4544277194
-
Combretastatin A4 phosphate: Background and current clinical status
-
DOI 10.1517/13543784.13.9.1171
-
Young, S. L.; Chaplin, D. J. Combretastatin A4 phosphate: background and current clinical status Expert Opin. Invest. Drugs 2004, 13, 1171-1182 (Pubitemid 39242740)
-
(2004)
Expert Opinion on Investigational Drugs
, vol.13
, Issue.9
, pp. 1171-1182
-
-
Young, S.L.1
Chaplin, D.J.2
-
34
-
-
77956301345
-
Combretastatin A4 phosphate: A novel vascular disrupting agent
-
Nagaiah, G.; Remick, S. C. Combretastatin A4 phosphate: a novel vascular disrupting agent Future Oncol. 2010, 6, 1219-1228
-
(2010)
Future Oncol.
, vol.6
, pp. 1219-1228
-
-
Nagaiah, G.1
Remick, S.C.2
-
35
-
-
77950976702
-
Disrupting established tumor blood vessels: An emerging therapeutic strategy for cancer
-
McKeage, M. J.; Baguley, B. C. Disrupting established tumor blood vessels: an emerging therapeutic strategy for cancer Cancer 2010, 116, 1859-1871
-
(2010)
Cancer
, vol.116
, pp. 1859-1871
-
-
McKeage, M.J.1
Baguley, B.C.2
-
36
-
-
36749043820
-
Tumour targeting by microtubule-depolymerising vascular disrupting agents
-
DOI 10.1517/14728222.11.11.1443
-
Kanthou, C.; Tozer, G. M. Tumour targeting by microtubule-depolymerising vascular disrupting agents Expert Opin. Ther. Targets 2007, 11, 1443-1457 (Pubitemid 350200480)
-
(2007)
Expert Opinion on Therapeutic Targets
, vol.11
, Issue.11
, pp. 1443-1457
-
-
Kanthou, C.1
Tozer, G.M.2
-
37
-
-
65249123159
-
Antivascular actions of microtubule-binding drugs
-
Schwartz, E. L. Antivascular actions of microtubule-binding drugs Clin. Cancer Res. 2009, 15, 2595-2601
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 2595-2601
-
-
Schwartz, E.L.1
-
39
-
-
65549090459
-
A review and update of the current status of the vasculature-disabling agent combretastatin-A4 phosphate (CA4P)
-
Siemann, D. W.; Chaplin, D. J.; Walicke, P. A. A review and update of the current status of the vasculature-disabling agent combretastatin-A4 phosphate (CA4P) Expert Opin. Invest. Drugs 2009, 18, 189-197
-
(2009)
Expert Opin. Invest. Drugs
, vol.18
, pp. 189-197
-
-
Siemann, D.W.1
Chaplin, D.J.2
Walicke, P.A.3
-
42
-
-
80052363744
-
-
IPCS INCHEM. Colchicine
-
IPCS INCHEM. Colchicine. http://www.inchem.org/documents/pims/pharm/ colchic.htm.
-
-
-
-
43
-
-
0025372840
-
N -Acetylcolchicinol O -methyl ether and thiocolchicine, potent analogs of colchicine modified in the C ring
-
Kang, G.-J.; Getahun, Z.; Muzaffar, A.; Brossi, A.; Hamel, E. N -Acetylcolchicinol O -methyl ether and thiocolchicine, potent analogs of colchicine modified in the C ring J. Biol. Chem. 1990, 256, 10255-10259
-
(1990)
J. Biol. Chem.
, vol.256
, pp. 10255-10259
-
-
Kang, G.-J.1
Getahun, Z.2
Muzaffar, A.3
Brossi, A.4
Hamel, E.5
-
44
-
-
33845579871
-
Colchicine today
-
DOI 10.1016/j.jbspin.2006.03.006, PII S1297319X06001837
-
Niel, E.; Scherrmann, J.-M. Colchicine today Jt., Bone, Spine 2006, 73, 672-678 (Pubitemid 44932240)
-
(2006)
Joint Bone Spine
, vol.73
, Issue.6
, pp. 672-678
-
-
Niel, E.1
Scherrmann, J.-M.2
-
45
-
-
0036890746
-
ZD6126: A novel small molecule vascular targeting agent
-
DOI 10.1016/S0360-3016(02)03922-6, PII S0360301602039226
-
Blakey, D. C.; Ashton, S. E.; Westwood, F. R.; Walker, M.; Anderson, J. R. ZD6126: a novel small molecule vascular targeting agent Int. J. Radiat. Oncol., Biol., Phys. 2002, 54, 1497-1502 (Pubitemid 35380055)
-
(2002)
International Journal of Radiation Oncology Biology Physics
, vol.54
, Issue.5
, pp. 1497-1502
-
-
Blakey, D.C.1
Ashton, S.E.2
Westwood, F.R.3
Walker, M.4
Ryan, A.J.5
-
46
-
-
0037115398
-
ZD6126: A novel vascular-targeting agent that causes selective destruction of tumor vasculature
-
Davis, P. D.; Dougherty, G. J.; Blakey, D. C.; Galbraith, S. M.; Tozer, G. M.; Holder, A. L.; Naylor, M. A.; Nolan, J.; Stratford, M. R. L.; Chaplin, D. J.; Hill, S. A. ZD6126: a novel vascular-targeting agent that causes selective destruction of tumor vasculature Cancer Res. 2002, 62, 7247-7253 (Pubitemid 36025246)
-
(2002)
Cancer Research
, vol.62
, Issue.24
, pp. 7247-7253
-
-
Davis, P.D.1
Dougherty, G.J.2
Blakey, D.C.3
Galbraith, S.M.4
Tozer, G.M.5
Holder, A.L.6
Naylor, M.A.7
Nolan, J.8
Stratford, M.R.L.9
Chaplin, D.J.10
Hill, S.A.11
-
47
-
-
40549125995
-
Phase i clinical evaluation of ZD6126, a novel vascular-targeting agent, in patients with solid tumors
-
LoRusso, P. M.; Gadgeel, S. M.; Wozniak, A.; Barge, A. J.; Jones, H. K.; DelProposto, Z. S.; DeLuca, P. A.; Evelhoch, J. L.; Boerner, S. A.; Wheeler, C. Phase I clinical evaluation of ZD6126, a novel vascular-targeting agent, in patients with solid tumors Invest. New Drugs 2008, 26, 159-167
-
(2008)
Invest. New Drugs
, vol.26
, pp. 159-167
-
-
Lorusso, P.M.1
Gadgeel, S.M.2
Wozniak, A.3
Barge, A.J.4
Jones, H.K.5
Delproposto, Z.S.6
Deluca, P.A.7
Evelhoch, J.L.8
Boerner, S.A.9
Wheeler, C.10
-
48
-
-
33645732100
-
Phase i clinical evaluation of weekly administration of the novel vascular-targeting agent, ZD6126, in patients with solid tumors
-
Beerepoot, L. V.; Radema, S. A.; Witteveen, E. O.; Thomas, T.; Wheeler, C.; Kempin, S.; Voest, E. E. Phase I clinical evaluation of weekly administration of the novel vascular-targeting agent, ZD6126, in patients with solid tumors J. Clin. Onocol. 2006, 24, 1492-1498
-
(2006)
J. Clin. Onocol.
, vol.24
, pp. 1492-1498
-
-
Beerepoot, L.V.1
Radema, S.A.2
Witteveen, E.O.3
Thomas, T.4
Wheeler, C.5
Kempin, S.6
Voest, E.E.7
-
49
-
-
77951667223
-
A phase Ib trial of CA4P (combretastatin A-4 phosphate), carboplatin, and paclitaxel in patients with advanced cancer
-
references therein
-
Rustin, G. J.; Shreeves, G.; Nathan, P. D.; Gaya, A.; Ganesan, T. S.; Wang, D.; Boxall, J.; Poupard, L.; Chaplin, D. J.; Stratford, M. R. L.; Balkissoon, J.; Zweifel, M. A phase Ib trial of CA4P (combretastatin A-4 phosphate), carboplatin, and paclitaxel in patients with advanced cancer Br. J. Cancer 2010, 102, 1355-1360 and references therein
-
(2010)
Br. J. Cancer
, vol.102
, pp. 1355-1360
-
-
Rustin, G.J.1
Shreeves, G.2
Nathan, P.D.3
Gaya, A.4
Ganesan, T.S.5
Wang, D.6
Boxall, J.7
Poupard, L.8
Chaplin, D.J.9
Stratford, M.R.L.10
Balkissoon, J.11
Zweifel, M.12
-
50
-
-
77955978648
-
Phase i trial of CYT997, a novel cytotoxic and vascular disrupting agent
-
Lickliter, J. D.; Francesconi, A. B.; Smith, G.; Burge, M.; Coulthard, A.; Rose, S.; Griffin, M.; Milne, R.; McCarron, J.; Yeadon, T.; Wilks, A.; Cubitt, A.; Wyld, D. K.; Vasey, P. A. Phase I trial of CYT997, a novel cytotoxic and vascular disrupting agent Br. J. Cancer 2010, 103, 597-606
-
(2010)
Br. J. Cancer
, vol.103
, pp. 597-606
-
-
Lickliter, J.D.1
Francesconi, A.B.2
Smith, G.3
Burge, M.4
Coulthard, A.5
Rose, S.6
Griffin, M.7
Milne, R.8
McCarron, J.9
Yeadon, T.10
Wilks, A.11
Cubitt, A.12
Wyld, D.K.13
Vasey, P.A.14
-
51
-
-
78650376933
-
Phase 1 first-in-human trial of the vascular disrupting agent plinabulin (NPI-2358) in patients with solid tumors or lymphomas
-
Mita, M. M.; Spear, M. A.; Yee, L. K.; Mita, A. C.; Heath, E. I.; Papadopoulos, K. P.; Federico, K. C.; Reich, S. D.; Romero, O.; Malburg, L.; Pilat, M.-J.; Lloyd, G. K.; Neuteboom, S. T. C.; Cropp, G.; Ashton, E.; LoRusso, P. M. Phase 1 first-in-human trial of the vascular disrupting agent plinabulin (NPI-2358) in patients with solid tumors or lymphomas Clin. Cancer Res. 2010, 16, 5892-5899
-
(2010)
Clin. Cancer Res.
, vol.16
, pp. 5892-5899
-
-
Mita, M.M.1
Spear, M.A.2
Yee, L.K.3
Mita, A.C.4
Heath, E.I.5
Papadopoulos, K.P.6
Federico, K.C.7
Reich, S.D.8
Romero, O.9
Malburg, L.10
Pilat, M.-J.11
Lloyd, G.K.12
Neuteboom, S.T.C.13
Cropp, G.14
Ashton, E.15
Lorusso, P.M.16
-
52
-
-
78149418659
-
ASA404: A tumor vascular-disrupting agent with broad potential for cancer therapy
-
Baguley, B. C.; McKeage, M. J. ASA404: a tumor vascular-disrupting agent with broad potential for cancer therapy Future Oncol. 2010, 6, 1537-1543
-
(2010)
Future Oncol.
, vol.6
, pp. 1537-1543
-
-
Baguley, B.C.1
McKeage, M.J.2
-
53
-
-
34247249906
-
Vascular disrupting agents in clinical development
-
DOI 10.1038/sj.bjc.6603694, PII 6603694
-
Hinnen, P.; Eskens, F. A. L. M. Vascular disrupting agents in clinical development Br. J. Cancer 2007, 96, 1159-1165 (Pubitemid 46625071)
-
(2007)
British Journal of Cancer
, vol.96
, Issue.8
, pp. 1159-1165
-
-
Hinnen, P.1
Eskens, F.A.L.M.2
-
54
-
-
33845286942
-
Vascular disrupting agents
-
Lippert, J. W. Vascular disrupting agents Bioorg. Med. Chem. 2007, 15, 605-615
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 605-615
-
-
Lippert, J.W.1
-
55
-
-
33750504410
-
Morphologic Manifestations of Vascular-Disrupting Agents in Preclinical Models
-
Siemann, D. W. John Wiley and Sons: New York
-
Rojiani, M. V.; Rojiani, A. M. Morphologic Manifestations of Vascular-Disrupting Agents in Preclinical Models. In Vascular-Targeted Therapies in Oncology; Siemann, D. W., Ed.; John Wiley and Sons: New York, 2006; pp 81-94.
-
(2006)
Vascular-Targeted Therapies in Oncology
, pp. 81-94
-
-
Rojiani, M.V.1
Rojiani, A.M.2
-
56
-
-
33846204064
-
Combined Modality Approaches Using Vasculature-Disrupting Agents
-
Siemann, D. W. John Wiley and Sons: New York
-
Shi, W.; Horsman, M. R.; Siemann, D. W. Combined Modality Approaches Using Vasculature-Disrupting Agents. In Vascular-Targeted Therapies in Oncology; Siemann, D. W., Ed.; John Wiley and Sons: New York, 2006; pp 123-136.
-
(2006)
Vascular-Targeted Therapies in Oncology
, pp. 123-136
-
-
Shi, W.1
Horsman, M.R.2
Siemann, D.W.3
-
57
-
-
0038576983
-
Oxi4503, a novel vascular targeting agent: Effects on blood flow and antitumor activity in comparison to combretastatin A-4 phosphate
-
Hua, J.; Sheng, Y.; Pinney, K. G.; Garner, C. M.; Kane, R. R.; Prezioso, J. A.; Pettit, G. R.; Chaplin, D. J.; Edvardsen, K. Oxi4503, a novel vascular targeting agent: effects on blood flow and antitumor activity in comparison to combretastatin A-4 phosphate Anticancer Res. 2003, 23, 1433-1440 (Pubitemid 36754111)
-
(2003)
Anticancer Research
, vol.23
, Issue.2 B
, pp. 1433-1440
-
-
Hua, J.1
Sheng, Y.2
Pinney, K.G.3
Garner, C.M.4
Kane, R.R.5
Prezioso, J.A.6
Pettit, G.R.7
Chaplin, D.J.8
Edvardsen, K.9
-
58
-
-
77953423945
-
BNC105: A novel tubulin polymerization inhibitor that selectively disrupts tumor vasculature and displays single-agent antitumor efficacy
-
Kremmidiotis, G.; Leske, A. F.; Lavranos, T. C.; Beaumont, D.; Gasic, J.; Hall, A.; O'Callaghan, M.; Matthews, C. A.; Flynn, B. L. BNC105: a novel tubulin polymerization inhibitor that selectively disrupts tumor vasculature and displays single-agent antitumor efficacy Mol. Cancer Ther. 2010, 9, 1562-1573
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 1562-1573
-
-
Kremmidiotis, G.1
Leske, A.F.2
Lavranos, T.C.3
Beaumont, D.4
Gasic, J.5
Hall, A.6
O'callaghan, M.7
Matthews, C.A.8
Flynn, B.L.9
-
60
-
-
80052387507
-
-
PCT Int. Appl. WO2007087684
-
Chaplin, J. H.; Gill, G. S.; Grobelny, D. W.; Flynn, B. L.; Kremmidiotis, G. Substituted Benzofurans, Benzothiophenes, Benzoselenophenes and Indoles and Their Use as Tubulin Polymerization Inhibitors. PCT Int. Appl. WO2007087684, 2007.
-
(2007)
Substituted Benzofurans, Benzothiophenes, Benzoselenophenes and Indoles and Their Use As Tubulin Polymerization Inhibitors
-
-
Chaplin, J.H.1
Gill, G.S.2
Grobelny, D.W.3
Flynn, B.L.4
Kremmidiotis, G.5
-
61
-
-
0033583499
-
A new anti-tubulin agent containing the benzo[b]thiophene ring system
-
DOI 10.1016/S0960-894X(99)00143-2, PII S0960894X99001432
-
Pinney, K. G.; Bounds, A. D.; Dingeman, K. M.; Mocharla, V. P.; Pettit, G. R.; Bai, R.; Hamel, E. A new anti-tubulin agent containing the benzo[ b ]thiophene ring system Bioorg. Med. Chem. Lett. 1999, 9, 1081-1086 (Pubitemid 29204661)
-
(1999)
Bioorganic and Medicinal Chemistry Letters
, vol.9
, Issue.8
, pp. 1081-1086
-
-
Pinney, K.G.1
Bounds, A.D.2
Dingeman, K.M.3
Mocharla, V.P.4
Pettit, G.R.5
Bai, R.6
Hamel, E.7
-
62
-
-
0032378223
-
Characterization and structural analyses of trimethoxy and triethoxybenzo[b]thiophene
-
Mullica, D. F.; Pinney, K. G.; Mocharla, V. P.; Dingeman, K. M.; Bounds, A. D.; Sappenfield, E. L. Characterization and structural analyses of trimethoxy and triethoxybenzo[ b ]thiophene J. Chem. Crystallogr. 1998, 28, 289-295 (Pubitemid 128364746)
-
(1998)
Journal of Chemical Crystallography
, vol.28
, Issue.4
, pp. 289-295
-
-
Mullica, D.F.1
Pinney, K.G.2
Mocharla, V.P.3
Dingeman, K.M.4
Bounds, A.D.5
Sappenfield, E.L.6
-
63
-
-
0035826341
-
A novel palladium - Mediated coupling approach to 2,3 - Disubstituted benzo[ b ]thiophenes and its application to the synthesis of tubulin binding agents
-
Flynn, B. L.; Verdier-Pinard, P.; Hamel, E. A novel palladium-mediated coupling approach to 2,3-disubstituted benzo[ b ]thiophenes and its application to the synthesis of tubulin binding agents Org. Lett. 2001, 3, 651-654
-
(2001)
Org. Lett.
, vol.3
, pp. 651-654
-
-
Flynn, B.L.1
Verdier-Pinard, P.2
Hamel, E.3
-
64
-
-
0035801759
-
The synthesis and tubulin binding activity of thiophene-based analogues of combretastatin A-4
-
DOI 10.1016/S0960-894X(01)00436-X, PII S0960894X0100436X
-
Flynn, B. L.; Flynn, G. P.; Hamel, E.; Jung, M. K. The synthesis and tubulin binding activity of thiophene-based analogues of combretastatin A-4 Bioorg. Med. Chem. Lett. 2001, 11, 2341-2343 (Pubitemid 32781695)
-
(2001)
Bioorganic and Medicinal Chemistry Letters
, vol.11
, Issue.17
, pp. 2341-2343
-
-
Flynn, B.L.1
Flynn, G.P.2
Hamel, E.3
Jung M.Katherine4
-
65
-
-
0037030605
-
One-pot synthesis of benzo[b]furan and indole inhibitors of tubulin polymerization
-
DOI 10.1021/jm020077t
-
Flynn, B. L.; Hamel, E.; Jung, M. K. A one-pot synthesis of benzo[ b ]furan and indole inhibitors of tubulin polymerization J. Med. Chem. 2002, 45, 2670-2673 (Pubitemid 34595238)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.12
, pp. 2670-2673
-
-
Flynn, B.L.1
Hamel, E.2
Jung, M.K.3
-
66
-
-
33947717991
-
The concise synthesis of chalcone, indanone and indenone analogues of combretastatin A4
-
DOI 10.1016/j.bmc.2007.02.006, PII S0968089607001101
-
Related indenones I (X = carbonyl) are inactive: Kerr, D. J.; Hamel, E.; Jung, M. K.; Flynn, B. L. The concise synthesis of chalcone, indanone and indenone analogues of combretastatin A4 Bioorg. Med. Chem. 2007, 15, 3290-3298 (Pubitemid 46505268)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.9
, pp. 3290-3298
-
-
Kerr, D.J.1
Hamel, E.2
Jung, M.K.3
Flynn, B.L.4
-
67
-
-
3843136376
-
Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents
-
DOI 10.1021/jm049802l
-
Liou, J.-P.; Chang, Y.-C.; Kuo, F.-M.; Chang, C-.W.; Tseng, H.-Y.; Wang, C.-C.; Yang, Y.-N.; Chang, J.-Y.; Lee, S.-J.; Hsieh, H. P. Concise synthesis and structure-activity relationships of combretastatins A-4 analogues, 1-aroylindoles and 3-aroylindoles, a novel class of potent antitubulin agents J. Med. Chem. 2004, 47, 4247-4257 (Pubitemid 39045430)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.17
, pp. 4247-4257
-
-
Liou, J.-P.1
Chang, Y.-L.2
Kuo, F.-M.3
Chang, C.-W.4
Tseng, H.-Y.5
Wang, C.-C.6
Yang, Y.-N.7
Chang, J.-Y.8
Lee, S.-J.9
Hsieh, H.-P.10
-
68
-
-
0035823347
-
A multi-component coupling approach to benzo[b]furans and indoles
-
Chaplin, J. H.; Flynn, B. L. A multi-component coupling approach to benzo[ b ]furans and indoles J. Chem. Soc., Chem. Commun. 2001, 1594-1595 (Pubitemid 32808010)
-
(2001)
Chemical Communications
, Issue.17
, pp. 1594-1595
-
-
Chaplin, J.H.1
Flynn, B.L.2
-
69
-
-
38849184650
-
An efficient synthesis and substitution of 3-aroyl-2-bromobenzo[b]furans
-
DOI 10.1021/jo701656z
-
Gill, G. S.; Grobelny, D. W.; Chaplin, J. H.; Flynn, B. L. An efficient synthesis and substitution of 3-aroyl-2-bromobenzo[ b ]furans J. Org. Chem. 2008, 73, 1131-1134 (Pubitemid 351198764)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.3
, pp. 1131-1134
-
-
Gill, G.S.1
Grobelny, D.W.2
Chaplin, J.H.3
Flynn, B.L.4
-
70
-
-
0029042650
-
Synthesis of aromatic heterocycles via palladium-catalyzed annulation of internal alkynes
-
Larock, R. C.; Yum, E. K.; Doty, M. J.; Sham, K. C. Synthesis of aromatic heterocycles via palladium-catalyzed annulation of internal alkynes J. Org. Chem. 1995, 60, 3270-3271
-
(1995)
J. Org. Chem.
, vol.60
, pp. 3270-3271
-
-
Larock, R.C.1
Yum, E.K.2
Doty, M.J.3
Sham, K.C.4
-
71
-
-
0038718703
-
Altered angiogenesis and survival in human tumor-derived endothelial cells
-
Bussolati, B.; Deambrosis, I.; Russo, S.; Deregibus, M. C.; Camussi, G. Altered angiogenesis and survival in human tumor-derived endothelial cells FASEB J. 2003, 17, 1159-1161
-
(2003)
FASEB J.
, vol.17
, pp. 1159-1161
-
-
Bussolati, B.1
Deambrosis, I.2
Russo, S.3
Deregibus, M.C.4
Camussi, G.5
-
72
-
-
15144356733
-
Novel combretastatin analogues effective against murine solid tumors: Design and structure-activity relationships
-
DOI 10.1021/jm980101w
-
Ohsumi, K.; Nakagawa, R.; Fukuda, Y.; Hatanaka, T.; Morinaga, Y.; Nihei, Y.; Ohishi, K.; Suga, Y.; Akiyama, Y.; Tsuji, T. Novel combretastatin analogues effective against murine solid tumors: design and structure-activity relationships J. Med. Chem. 1998, 41, 3022-3032 (Pubitemid 28359938)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.16
, pp. 3022-3032
-
-
Ohsumi, K.1
Nakagawa, R.2
Fukuda, Y.3
Hatanaka, T.4
Morinaga, Y.5
Nihei, Y.6
Ohishi, K.7
Suga, Y.8
Akiyama, Y.9
Tsuji, T.10
-
73
-
-
19944433930
-
Further naphthylcombretastatins. An investigation on the role of the naphthalene moiety
-
DOI 10.1021/jm0310737
-
Maya, A. B. S.; Perez-Melero, C.; Mateo, C.; Alonso, D.; Fernandez, J. L.; Gajate, C.; Mollinedo, F.; Pelaez, R.; Caballero, E.; Medarde, M. Further naphthylcombretastatins. An investigation on the role of the naphthalene moiety J. Med. Chem. 2005, 48, 556-568 (Pubitemid 40139798)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.2
, pp. 556-568
-
-
Maya, A.B.S.1
Perez-Melero, C.2
Mateo, C.3
Alonso, D.4
Fernandez, J.L.5
Gajate, C.6
Mollinedo, F.7
Pelaez, R.8
Caballero, E.9
Medarde, M.10
-
74
-
-
0026047751
-
Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization
-
Cushman, M.; Nagarathnam, D.; Gopal, D.; Chakraborti, A. K.; Lin, C. M.; Hamel, E. Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization J. Med. Chem. 1991, 34, 2579-2588
-
(1991)
J. Med. Chem.
, vol.34
, pp. 2579-2588
-
-
Cushman, M.1
Nagarathnam, D.2
Gopal, D.3
Chakraborti, A.K.4
Lin, C.M.5
Hamel, E.6
-
75
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
DOI 10.1038/nature02393
-
Ravelli, R. B. G.; Gigant, G.; Curmi, P. A.; Jourdain, I.; Lachkar, S.; Sobel, A.; Knossow, M. Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain Nature 2004, 428, 198-202 (Pubitemid 38374318)
-
(2004)
Nature
, vol.428
, Issue.6979
, pp. 198-202
-
-
Ravelli, R.B.G.1
Gigant, B.2
Curmi, P.A.3
Jourdain, I.4
Lachkar, S.5
Sobel, A.6
Knossow, M.7
-
76
-
-
33750124980
-
Extra precision glide: Docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes
-
DOI 10.1021/jm051256o
-
Friesner, R. A.; Murphy, R. B.; Repasky, M. P.; Frye, L. L.; Greenwood, J. R.; Halgren, T. A.; Sanschagrin, P. C.; Mainz, D. T. Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes J. Med. Chem. 2006, 49, 6177-6196 (Pubitemid 44595196)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.21
, pp. 6177-6196
-
-
Friesner, R.A.1
Murphy, R.B.2
Repasky, M.P.3
Frye, L.L.4
Greenwood, J.R.5
Halgren, T.A.6
Sanschagrin, P.C.7
Mainz, D.T.8
-
77
-
-
60849122543
-
Toward docking-based virtual screening for discovering antitubulin agents by targeting taxane and colchicines binding sites
-
For other docking studies on tubulin see the following: and references cited therein
-
For other docking studies on tubulin see the following: Soulère, L. Toward docking-based virtual screening for discovering antitubulin agents by targeting taxane and colchicines binding sites ChemMedChem 2009, 4, 161-163 and references cited therein
-
(2009)
ChemMedChem
, vol.4
, pp. 161-163
-
-
Soulère, L.1
-
78
-
-
65649131520
-
Multidrug resistance through the spectacle of P-glycoprotein
-
Goda, K.; Bacso, Z.; Szabo, G. Multidrug resistance through the spectacle of P-glycoprotein Curr. Cancer Drug Targets 2009, 9, 281-297
-
(2009)
Curr. Cancer Drug Targets
, vol.9
, pp. 281-297
-
-
Goda, K.1
Bacso, Z.2
Szabo, G.3
-
79
-
-
0242267919
-
Synthesis and Biological Evaluation of 2′-Taxoids Derived from Baccatin III and 14β-OH-Baccatin III 1,14-Carbonate
-
Battaglia, A.; Bernacki, R. J.; Bertucci, C.; Bombardelli, E.; Cimitan, S.; Ferlini, C.; Fontana, G.; Guerrini, A.; Riva, A. Synthesis and biological evaluation of 2′-methyl taxoids derived from baccatin III and 14β-OH-baccatin III 1,14-carbonate J. Med. Chem. 2003, 46, 4822-4825 (Pubitemid 37352020)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.23
, pp. 4822-4825
-
-
Battaglia, A.1
Bernacki, R.J.2
Bertucci, C.3
Bombardelli, E.4
Cimitan, S.5
Ferlini, C.6
Fontana, G.7
Guerrini, A.8
Riva, A.9
-
80
-
-
77951182123
-
Lovastatin induces apoptosis of ovarian cancer cells and synergizes with doxorubicin: Potential therapeutic relevance
-
Martirosyan, A.; Clendening, J. W.; Goard, C. A.; Penn, L. Z. Lovastatin induces apoptosis of ovarian cancer cells and synergizes with doxorubicin: potential therapeutic relevance BMC Cancer 2010, 10, 103
-
(2010)
BMC Cancer
, vol.10
, pp. 103
-
-
Martirosyan, A.1
Clendening, J.W.2
Goard, C.A.3
Penn, L.Z.4
-
81
-
-
0031980124
-
Antineoplastic agents 389. New syntheses of the combretastatin A-4 prodrug
-
Pettit, G. R.; Rhodes, M. R. Antineoplastic agents 389. New syntheses of the combretastatin A-4 prodrug Anti-Cancer Drug Des. 1998, 13, 183-191 (Pubitemid 28188203)
-
(1998)
Anti-Cancer Drug Design
, vol.13
, Issue.3
, pp. 183-191
-
-
Pettit, G.R.1
Rhodes, M.R.2
-
82
-
-
80052385731
-
-
Bionomics. BNC105
-
Bionomics. BNC105. http://www.bionomics.com.au/page.php?section=103.
-
-
-
-
83
-
-
0021163546
-
Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization
-
Hamel, E.; Lin, C. M. Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization Biochemistry 1984, 23, 4173-4184
-
(1984)
Biochemistry
, vol.23
, pp. 4173-4184
-
-
Hamel, E.1
Lin, C.M.2
-
84
-
-
0142036683
-
Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin
-
Hamel, E. Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin Cell Biochem. Biophys. 2003, 38, 1-22
-
(2003)
Cell Biochem. Biophys.
, vol.38
, pp. 1-22
-
-
Hamel, E.1
-
85
-
-
0031913357
-
Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells
-
Verdier-Pinard, P.; Lai, J.-Y.; Yoo, H.-D.; Yu, J.; Márquez, B.; Nagle, D. G.; Nambu, M.; White, J. D.; Falck, J. R.; Gerwick, W. H.; Day, B. W.; Hamel, E. Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells Mol. Pharmacol. 1998, 53, 62-76 (Pubitemid 28068373)
-
(1998)
Molecular Pharmacology
, vol.53
, Issue.1
, pp. 62-76
-
-
Verdier-Pinard, P.1
Lai, J.-Y.2
Yoo, H.-D.3
Yu, J.4
Marquez, B.5
Nagle, D.G.6
Nambu, M.7
White, J.D.8
Falck, J.R.9
Gerwick, W.H.10
Day, B.W.11
Hamel, E.12
|