-
1
-
-
33749258555
-
Novel imidazolebased combretastatin a-4 analogues: Evaluation of their in vitro antitumor activity and molecular modelling study of their binding to the colchicine site of tubulin
-
Bellina F, Cauteruccio S, Monti S, Rossi R (2006) Novel imidazolebased combretastatin A-4 analogues: evaluation of their in vitro antitumor activity and molecular modelling study of their binding to the colchicine site of tubulin. Bioorg Med Chem Lett 16:5757-5762
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 5757-5762
-
-
Bellina, F.1
Cauteruccio, S.2
Monti, S.3
Rossi, R.4
-
2
-
-
37049074864
-
Synthesis of water-soluble sugar derivatives of combretastatin a-4
-
Brown RT, Fox BW, Hadfield JA, McGown AT, Mayalarp SP, Pettit GR, Woods JA (1995) Synthesis of water-soluble sugar derivatives of combretastatin A-4. J Chem Soc Perkin Trans 1:577-582
-
(1995)
J Chem Soc Perkin Trans
, vol.1
, pp. 577-582
-
-
Brown, R.T.1
Fox, B.W.2
Hadfield, J.A.3
McGown, A.T.4
Mayalarp, S.P.5
Pettit, G.R.6
Woods, J.A.7
-
3
-
-
84871460753
-
-
Cambridge ChemDraw Ultra 6.0 and Chem3D Ultra
-
ChemDraw Ultra 6.0 and Chem3D Ultra (2000) Cambridge Soft Corporation, Cambridge
-
(2000)
Cambridge Soft Corporation
-
-
-
4
-
-
84871441945
-
Stilbene derivatives as anticancer agents
-
Cushman MS, Layfayette W, Hamel E, Bethesda (1995) Stilbene derivatives as anticancer agents. United States Patent. Patent no 5,430,062
-
(1995)
United States Patent. Patent
, Issue.5430
, pp. 062
-
-
Cushman, M.S.1
Layfayette, W.2
Hamel, E.3
Bethesda4
-
5
-
-
72049105856
-
Combretastatin-like chalcones as inhibitors of microtubule polymerisation part 2: Structure-based discovery of alpha-Aryl chalcones
-
Ducki S, Mackenzie G, Greedy B, Armitage S, Chabert JF, Bennett E, Nettles J, Snyder JP, Lawrence NJ (2009) Combretastatin-like chalcones as inhibitors of microtubule polymerisation. Part 2: Structure-based discovery of alpha-Aryl chalcones. Bioorg Med Chem 17:7711-7722
-
(2009)
Bioorg Med Chem
, vol.17
, pp. 7711-7722
-
-
Ducki, S.1
Mackenzie, G.2
Greedy, B.3
Armitage, S.4
Chabert, J.F.5
Bennett, E.6
Nettles, J.7
Snyder, J.P.8
Lawrence, N.J.9
-
6
-
-
71849087235
-
Synthesis and antitumor-evaluation of cyclopropyl-containing combretastatin analogs
-
Furst R, Zupko I, Berenyi A, Ecker GF, Rinner U (2009) Synthesis and antitumor-evaluation of cyclopropyl-containing combretastatin analogs. Bioorg Med Chem Lett 19:6948-6951
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 6948-6951
-
-
Furst, R.1
Zupko, I.2
Berenyi, A.3
Ecker, G.F.4
Rinner, U.5
-
7
-
-
84871451656
-
-
GOLD Cambridge Crystallographic Data Centre, Cambridge
-
GOLD (2009) Evaluation version 4.0.1. Cambridge Crystallographic Data Centre, Cambridge
-
(2009)
Evaluation Version 4.0.1
-
-
-
9
-
-
33646492299
-
Isoxazole-type derivatives related to combretastatin a-4, synthesis and biological evaluation
-
Kaffy J, Pontikis R, Carrz D, Croisy A, Monneret C, Florent JC (2006) Isoxazole-type derivatives related to combretastatin A-4, synthesis and biological evaluation. Bioorg Med Chem 14:4067-4077
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 4067-4077
-
-
Kaffy, J.1
Pontikis, R.2
Carrz, D.3
Croisy, A.4
Monneret, C.5
Florent, J.C.6
-
10
-
-
25144434945
-
Structure-based discovery of a boronic acid bioisostere of combretastatin a-4
-
Kong Y, Grembecka J, Edler MC, Hamel E, Mooberry SL, Sabat M, Rieger J, Brown ML (2005) Structure-based discovery of a boronic acid bioisostere of combretastatin A-4. Chem Biol 12:1007-1014
-
(2005)
Chem Biol
, vol.12
, pp. 1007-1014
-
-
Kong, Y.1
Grembecka, J.2
Edler, M.C.3
Hamel, E.4
Mooberry, S.L.5
Sabat, M.6
Rieger, J.7
Brown, M.L.8
-
11
-
-
51149096446
-
1,2,3,4-Tetrahydro-2-thioxopyrimidine analogs of combretastatin-A4
-
Lee L, Davis R, Vanderham J, Hills P, Mackay H, Brown T, Mooberry SL, Lee M (2008) 1,2,3,4-Tetrahydro-2-thioxopyrimidine analogs of combretastatin-A4. Eur J Med Chem 43:2011-2015
-
(2008)
Eur J Med Chem
, vol.43
, pp. 2011-2015
-
-
Lee, L.1
Davis, R.2
Vanderham, J.3
Hills, P.4
Mackay, H.5
Brown, T.6
Mooberry, S.L.7
Lee, M.8
-
12
-
-
3843136376
-
Concise synthesis and structure-Activity relationship of combretastatin a-4 analogues, 1-Aroylindoles, as novel classes of potent antitubulin agents
-
Liou JP, Chang YL, Kuo FM, Chang CW, Tseng HY, Wang CC, Yang YN, Chang JY, Lee SJ, Hsieh HP (2004) Concise synthesis and structure-Activity relationship of combretastatin A-4 analogues, 1-Aroylindoles, as novel classes of potent antitubulin agents. J Med Chem 47:4247-4257
-
(2004)
J Med Chem
, vol.47
, 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
-
13
-
-
47749140369
-
Discovery of 4-Amino and 4-hydroxy-1-Aroylindoles as potent tubulin polymerization inhibitors
-
Liou JP, Wu ZY, Kuo CC, Chang CY, Lu PY, Chen CM, Hsieh HP, Chang JY (2008) Discovery of 4-Amino and 4-hydroxy-1-Aroylindoles as potent tubulin polymerization inhibitors. J Med Chem 51:4351-4355
-
(2008)
J Med Chem
, vol.51
, pp. 4351-4355
-
-
Liou, J.P.1
Wu, Z.Y.2
Kuo, C.C.3
Chang, C.Y.4
Lu, P.Y.5
Chen, C.M.6
Hsieh, H.P.7
Chang, J.Y.8
-
14
-
-
0024510343
-
Structural and biochemical comparison of the anti-mitotic agents colchicine, combretastatin a4 and amphethinile
-
McGown AT, Fox BW (1989) Structural and biochemical comparison of the anti-mitotic agents colchicine, combretastatin A4 and amphethinile. Anticancer Drug Des 3:249-254
-
(1989)
Anticancer Drug Des
, vol.3
, pp. 249-254
-
-
McGown, A.T.1
Fox, B.W.2
-
15
-
-
0025775062
-
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
-
Monks A, Scudiero D, Skehan P, Shoemaker R, Paull K, Vistica D, Hose C, Langley J, Cronise P, Vaigro-Wolff A (1991) Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. J Natl Cancer Inst 83:757-766
-
(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-Wolff, A.10
-
16
-
-
0025804962
-
Quantitative structure-Activity relationship analysis of combretastatins: A class of novel antimitotic agents
-
Nandy P, Banerjee S, Gao H, Hui MB, Lien EJ (1991) Quantitative structure-Activity relationship analysis of combretastatins: A class of novel antimitotic agents. Pharm Res 8:776-781
-
(1991)
Pharm Res
, vol.8
, pp. 776-781
-
-
Nandy, P.1
Banerjee, S.2
Gao, H.3
Hui, M.B.4
Lien, E.J.5
-
17
-
-
31344448309
-
Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization and activity in tumor cell lines
-
Ouyang X, Piatnitski EL, Pattaropong V, Chen X, He HY, Kiselyov AS, Valankar A, Kwakami J, Labelle M, Smith L, Lohman J, Lee SP, Malikzay A, Fleming J, Gerlak J, Wang Y, Rosler RL, Zhou K, Mitelman S, Camara M, Surguladze D, Boody JF, Tuma MC (2006) Oxadiazole derivatives as a novel class of antimitotic agents: synthesis, inhibition of tubulin polymerization and activity in tumor cell lines. Bioorg Med Chem Lett 16:1191-1196
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 1191-1196
-
-
Ouyang, X.1
Piatnitski, E.L.2
Pattaropong, V.3
Chen, X.4
He, H.Y.5
Kiselyov, A.S.6
Valankar, A.7
Kwakami, J.8
Labelle, M.9
Smith, L.10
Lohman, J.11
Lee, S.P.12
Malikzay, A.13
Fleming, J.14
Gerlak, J.15
Wang, Y.16
Rosler, R.L.17
Zhou, K.18
Mitelman, S.19
Camara, M.20
Surguladze, D.21
Boody, J.F.22
Tuma, M.C.23
more..
-
18
-
-
0023065565
-
Isolation, structure and synthesis of combretastatin a-1 and b-, potent new inhibitors of microtubule assembly, derived from combretum caffrum
-
Pettit GR, Singh SB, Niven ML, Hamel E, Schmit JM (1987) Isolation, structure and synthesis of combretastatin A-1 and B-, potent new inhibitors of microtubule assembly, derived from Combretum caffrum. J Nat Prod 50:119-120
-
(1987)
J Nat Prod
, vol.50
, pp. 119-120
-
-
Pettit, G.R.1
Singh, S.B.2
Niven, M.L.3
Hamel, E.4
Schmit, J.M.5
-
19
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
Ravelli RB, Gigant B, Curmi PA, Jourdain I, Lachkar S, Sobel A, Knossow M (2004) Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain. Nature 428:198-202
-
(2004)
Nature
, vol.428
, pp. 198-202
-
-
Ravelli, R.B.1
Gigant, B.2
Curmi, P.A.3
Jourdain, I.4
Lachkar, S.5
Sobel, A.6
Knossow, M.7
-
20
-
-
67650663259
-
Introduction to cancer chemotherapeutics
-
Shewach DS, Kuchta RD (2009) Introduction to cancer chemotherapeutics. Chem Rev 109:2859-2861
-
(2009)
Chem Rev
, vol.109
, pp. 2859-2861
-
-
Shewach, D.S.1
Kuchta, R.D.2
-
21
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren JT, Bokesch H, Kenney S, Boyd MR (1990) New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst 82:1107-1112
-
(1990)
J Natl Cancer Inst
, vol.82
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scudiero, D.3
Monks, A.4
McMahon, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, H.8
Kenney, S.9
Boyd, M.R.10
-
22
-
-
3042702727
-
Quantitative analysis of d-24851, a novel anticancer agent, in human plasma and urine by liquid chromatography coupled with tandem mass spectrometry
-
Stokvis E, Nan-Offeringa L, Ouwehand M, Tibben MM, Rosing H, Schnaar Y, Grigat M, Romeis P, Schellens JTM, Beijnen JH (2004) Quantitative analysis of D-24851, a novel anticancer agent, in human plasma and urine by liquid chromatography coupled with tandem mass spectrometry. Cancer Treat Rev 18:1465-1471
-
(2004)
Cancer Treat Rev
, vol.18
, pp. 1465-1471
-
-
Stokvis, E.1
Nan-Offeringa, L.2
Ouwehand, M.3
Tibben, M.M.4
Rosing, H.5
Schnaar, Y.6
Grigat, M.7
Romeis, P.8
Schellens, J.T.M.9
Beijnen, J.H.10
-
23
-
-
84871417666
-
-
The Merck Index edition,Organic Name Reactions-324
-
The Merck Index (2006) Fourteenth edition, Organic Name Reactions-324
-
(2006)
Fourteenth
-
-
-
24
-
-
33744820579
-
Medicinal chemistry of combretastatin a4: Present and future directions
-
Tron GC, Pirali T, Sorba G, Pagliai F, Busacca S, Genazzani AA (2006) Medicinal chemistry of combretastatin A4: present and future directions. J Med Chem 49:3033-3044
-
(2006)
J Med Chem
, vol.49
, pp. 3033-3044
-
-
Tron, G.C.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
25
-
-
27644466314
-
Combretastatin a4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-cadherin signalling
-
Vincent L, Kermani P, Young LM, Cheng J, Zhang F, Shido K, Lam G, Bompais VH, Zhu Z, Hicklin DJ, Bohlen P, Chaplin DJ, May C, Raffi SJ (2005) Combretastatin A4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-cadherin signalling. Clin Investig 115:2992
-
(2005)
Clin Investig
, vol.115
, pp. 2992
-
-
Vincent, L.1
Kermani, P.2
Young, L.M.3
Cheng, J.4
Zhang, F.5
Shido, K.6
Lam, G.7
Bompais, V.H.8
Zhu, Z.9
Hicklin, D.J.10
Bohlen, P.11
Chaplin, D.J.12
May, C.13
Raffi, S.J.14
-
26
-
-
0028930050
-
The interaction with tubulin of a series of stilbenes based on combretastatin a-4
-
Woods JA, Hadfield JA, Pettit GR, Fox BW, McGown AT (1995) The interaction with tubulin of a series of stilbenes based on combretastatin A-4. Br J Cancer 71:705-711
-
(1995)
Br J Cancer
, vol.71
, pp. 705-711
-
-
Woods, J.A.1
Hadfield, J.A.2
Pettit, G.R.3
Fox, B.W.4
McGown, A.T.5
|