-
2
-
-
4344572092
-
Microtubule structure and its stabilisation
-
Amos, L. A. Microtubule structure and its stabilisation. Org. Biomol. Chem. 2004, 2, 2153-2160.
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 2153-2160
-
-
Amos, L.A.1
-
3
-
-
0042233662
-
Microtubule-interacting drugs for cancer treatment
-
Checchi, P. M.; Nettles, J. H.; Zhou, J.; Snyder, J. P.; Joshi, H. C. Microtubule-interacting drugs for cancer treatment. Trends Pharmacol. Sci. 2003, 24, 361-365.
-
(2003)
Trends Pharmacol. Sci.
, vol.24
, pp. 361-365
-
-
Checchi, P.M.1
Nettles, J.H.2
Zhou, J.3
Snyder, J.P.4
Joshi, H.C.5
-
4
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
Jordan, M. A.; Wilson, L. Microtubules as a target for anticancer drugs. Nature Rev. 2004, 4, 947-954.
-
(2004)
Nature Rev.
, vol.4
, pp. 947-954
-
-
Jordan, M.A.1
Wilson, L.2
-
5
-
-
0035834521
-
Refined structure of α,β-tubulin at 3.5 Å resolution
-
Lowe, J.; Li, H.; Downing, K. H.; Nogales, E. Refined structure of α,β-tubulin at 3.5 Å resolution. J. Mol. Biol. 2001, 313, 1045-1057.
-
(2001)
J. Mol. Biol.
, vol.313
, pp. 1045-1057
-
-
Lowe, J.1
Li, H.2
Downing, K.H.3
Nogales, E.4
-
6
-
-
19544393159
-
Structural basis for the regulation of tubulin by vinblastine
-
DOI 10.1038/nature03566
-
Gigant, B.; Wang, C.; Ravelli, R. B. G.; Roussi, F.; Steinmetz, M. O.; Curmi, P. A.; Sobel, A.; Knossow, M. Structural basis for the regulation of tubulin by vinblastine. Nature 2005, 435, 519-522. (Pubitemid 40734250)
-
(2005)
Nature
, vol.435
, Issue.7041
, pp. 519-522
-
-
Gigant, B.1
Wang, C.2
Ravelli, R.B.G.3
Roussi, F.4
Steinmetz, M.O.5
Curmi, P.A.6
Sobel, A.7
Knossow, M.8
-
7
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
DOI 10.1038/nature02393
-
Ravelli, R. B. G.; Gigant, B.; 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
-
8
-
-
33744820579
-
Medicinal chemistry of Combretastatin A4: Present and future directions
-
Cesare Tron, G.; 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.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3033-3044
-
-
Cesare Tron, G.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
9
-
-
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, 209-238.
-
(2007)
Med. Res. Rev.
, vol.27
, pp. 209-238
-
-
Brancale, A.1
Silvestri, R.2
-
10
-
-
0035924236
-
Synthetic 2- aroylindole derivatives as a new class of potent tubulin-inhibitory, antimitotic agents
-
(a) Mahboobi, S.; Pongratz, H.; Hufsky, H.; Hockemeyer, J.; Frieser, M.; Lyssenko, A.; Paper, D. H.; Bohmer, F.-D.; Fiebig, H. H.; Burger, A. M.; Baasner, S.; Beckers, T. Synthetic 2- aroylindole derivatives as a new class of potent tubulin-inhibitory, antimitotic agents. J. Med. Chem. 2001, 44, 4535-4553.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4535-4553
-
-
Mahboobi, S.1
Pongratz, H.2
Hufsky, H.3
Hockemeyer, J.4
Frieser, M.5
Lyssenko, A.6
Paper, D.H.7
Bohmer, F.-D.8
Fiebig, H.H.9
Burger, A.M.10
Baasner, S.11
Beckers, T.12
-
11
-
-
0036606778
-
2-Aroylindoles, a novel class of potent, orally active small molecule tubulin inhibitors
-
(b) Beckers, T.; Reissmann, T.; Schmidt, M.; Burger, A. M.; Fiebig, H. H.; Vanhoefer, U.; Pongratz, H.; Hufsky, H.; Hockemeyer, J.; Frieser, M.; Mahboobi, S. 2-Aroylindoles, a novel class of potent, orally active small molecule tubulin inhibitors. Cancer Res. 2002, 62, 3113-3119. (Pubitemid 34602403)
-
(2002)
Cancer Research
, vol.62
, Issue.11
, pp. 3113-3119
-
-
Beckers, T.1
Reissmann, T.2
Schmidt, M.3
Burger, A.M.4
Fiebig, H.H.5
Vanhoefer, U.6
Pongratz, H.7
Hufsky, H.8
Hockemeyer, J.9
Frieser, M.10
Mahboobi, S.11
-
12
-
-
0035133804
-
D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity
-
Bacher, G.; Nickel, B.; Emig, P.; Vanhoefer, U.; Seeber, S.; Shandra, A.; Klenner, T.; Beckers, T. D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity. Cancer Res. 2001, 61, 392-399. (Pubitemid 32106651)
-
(2001)
Cancer Research
, vol.61
, Issue.1
, pp. 392-399
-
-
Bacher, G.1
Nickel, B.2
Emig, P.3
Vanhoefer, U.4
Seeber, S.5
Shandra, A.6
Klenner, T.7
Beckers, T.8
-
13
-
-
3042740981
-
BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antimitotic activity in vivo
-
(a) Kuo, C.-C.; Hsieh, H.-P.; Pan, W.-Y.; Chen, C.-P.; Liou, J.-P.; Lee, S.-J.; Chang, Y.-L.; Chen, C.-T.; Chang, J.-Y. BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antimitotic activity in vivo. Cancer Res. 2004, 64, 4621-4628.
-
(2004)
Cancer Res.
, vol.64
, pp. 4621-4628
-
-
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, C.-T.8
Chang, J.-Y.9
-
14
-
-
33750339847
-
Structure-activity relationship studies of 3-aroylindoles as potent antimitotic agents
-
(b) Liou, J.-P.; Mahindroo, N.; Chang, C.- W.; Guo, F.-M.; Lee, S. X.-H.; Tan, U.-K.; Yeh, T.-K.; Kuo, C.-C.; Chang, Y.-W.; Lu, P.-H.; Tung, Y.-S.; Lin, K.-T.; Chang, J.-Y.; Hsieh, H.-P. Structure-activity relationship studies of 3-aroylindoles as potent antimitotic agents. ChemMedChem 2006, 1, 1106-1118.
-
(2006)
ChemMedChem
, vol.1
, pp. 1106-1118
-
-
Liou, J.-P.1
Mahindroo, N.2
Chang, C.W.3
Guo, F.-M.4
Lee, S.X.-H.5
Tan, U.-K.6
Yeh, T.-K.7
Kuo, C.-C.8
Chang, Y.-W.9
Lu, P.-H.10
Tung, Y.-S.11
Lin, K.-T.12
Chang, J.-Y.13
Hsieh, H.-P.14
-
15
-
-
0037030605
-
One-pot synthesis of benzo- [b]furan and indole inhibitors of tubulin polymerization
-
Flynn, B. L.; Hamel, E.; Jung, M. K. One-pot synthesis of benzo- [b]furan and indole inhibitors of tubulin polymerization. J. Med. Chem. 2002, 45, 2670-2673.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 2670-2673
-
-
Flynn, B.L.1
Hamel, E.2
Jung, M.K.3
-
16
-
-
10044236627
-
Arylthioindoles, potent inhibitors of tubulin polymerization
-
(a) De Martino, G.; La Regina, G.; Coluccia, A.; Edler, M. C.; Chiara Barbera, C.; Brancale, A.; Wilcox, E.; Hamel, E.; Artico, M.; Silvestri, R. Arylthioindoles, potent inhibitors of tubulin polymerization. J. Med. Chem. 2004, 47, 6120-6123.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6120-6123
-
-
De Martino, G.1
La Regina, G.2
Coluccia, A.3
Edler, M.C.4
Chiara Barbera, C.5
Brancale, A.6
Wilcox, E.7
Hamel, E.8
Artico, M.9
Silvestri, R.10
-
17
-
-
32344432249
-
New arylthioindoles: Potent inhibitors of tubulin polymerization. 2. Structure-activity relationships and molecular modeling studies
-
(b) De Martino, G.; Edler, M. C.; La Regina, G.; Coluccia, A.; Chiara Barbera, C.; Barrow, D.; Nicholson, R. I.; Chiosis, G.; Brancale, A.; Hamel, E.; Artico, M.; Silvestri, R. New arylthioindoles: potent inhibitors of tubulin polymerization. 2. Structure-activity relationships and molecular modeling studies. J. Med. Chem. 2006, 49, 6120-6123.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6120-6123
-
-
De Martino, G.1
Edler, M.C.2
La Regina, G.3
Coluccia, A.4
Chiara Barbera, C.5
Barrow, D.6
Nicholson, R.I.7
Chiosis, G.8
Brancale, A.9
Hamel, E.10
Artico, M.11
Silvestri, R.12
-
18
-
-
27144500947
-
Synthesis of fused heterocycles with a benzazepinone moiety via intramolecular Heck coupling
-
DOI 10.1016/j.tetlet.2005.09.122, PII S0040403905020976
-
(a) Putey, A.; Joucla, L.; Joseph, B. Synthesis of fused heterocycles with a benzazepinone moiety via intramolecular Heck coupling. Tetrahedron Lett. 2005, 46, 8177-8179. (Pubitemid 41501465)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.47
, pp. 8177-8179
-
-
Joucla, L.1
Putey, A.2
Joseph, B.3
-
19
-
-
33845534545
-
Synthesis of latonduine derivatives via intramolecular Heck reaction
-
DOI 10.1016/j.tet.2006.11.042, PII S0040402006018436
-
(b) Putey, A.; Joucla, L.; Picot, L.; Besson, T.; Joseph, B. Synthesis of latonduine derivatives via intramolecular Heck reaction. Tetrahedron 2007, 63, 867-879. (Pubitemid 44920335)
-
(2007)
Tetrahedron
, vol.63
, Issue.4
, pp. 867-879
-
-
Putey, A.1
Joucla, L.2
Picot, L.3
Besson, T.4
Joseph, B.5
-
20
-
-
45749137266
-
New C5-alkylated indolobenzazepinones acting as inhibitors of tubulin polymerization: Cytotoxic and antitumor activities
-
Keller, L.; Beaumont, S.; Liu, J.-M.; Thoret, S.; Bignon, J. S.; Wdzieczak-Bakala, J.; Dauban, P.; Dodd, R. H. New C5-alkylated indolobenzazepinones acting as inhibitors of tubulin polymerization: cytotoxic and antitumor activities. J. Med. Chem. 2008, 51, 3414-3421.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 3414-3421
-
-
Keller, L.1
Beaumont, S.2
Liu, J.-M.3
Thoret, S.4
Bignon, J.S.5
Wdzieczak-Bakala, J.6
Dauban, P.7
Dodd, R.H.8
-
21
-
-
33846918696
-
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
-
Alberico, D.; Scott, M. E.; Lautens, M. Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Chem. Rev. 2007, 107, 174-238.
-
(2007)
Chem. Rev.
, vol.107
, pp. 174-238
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
22
-
-
0037154814
-
Application of the palladium-catalyzed borylation/Suzuki coupling (BSC) reaction to the synthesis of biologically active biaryl lactams
-
(a) Baudoin, O.; Cesario, M.; Guénard, D.; Guéritte, F. Application of the palladium-catalyzed borylation/Suzuki coupling (BSC) reaction to the synthesis of biologically active biaryl lactams. J. Org. Chem. 2002, 67, 1199-1207.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 1199-1207
-
-
Baudoin, O.1
Cesario, M.2
Guénard, D.3
Guéritte, F.4
-
23
-
-
4644319019
-
An improved stereocontrolled route to cis-erythrinanes by combined intramolecular Strecker/Bruylants reaction
-
(b) Reimann, E.; Ettmayr, C. An improved stereocontrolled route to cis-erythrinanes by combined intramolecular Strecker/Bruylants reaction. Monatsh. Chem. 2004, 135, 1143-1155.
-
(2004)
Monatsh. Chem.
, vol.135
, pp. 1143-1155
-
-
Reimann, E.1
Ettmayr, C.2
-
24
-
-
54549117892
-
A mild inter- and intramolecular amination of aryl halides with a combination of CuI and CsOAc
-
(c) Kubo, T.; Katoh, C.; Yamada, K.; Okano, K.; Tokuyama, H.; Fukuyama, T. A mild inter- and intramolecular amination of aryl halides with a combination of CuI and CsOAc. Tetrahedron 2008, 64, 11230-11236.
-
(2008)
Tetrahedron
, vol.64
, pp. 11230-11236
-
-
Kubo, T.1
Katoh, C.2
Yamada, K.3
Okano, K.4
Tokuyama, H.5
Fukuyama, T.6
-
25
-
-
0000794778
-
Direct synthesis of benzo[c]phenanthridines and benzo[c]phenanthridones via SRN1 reactions
-
(a) Beugelmans, R.; Chastanet, J.; Ginsburg, H.; Quintero-Cortes, L.; Roussi, G. Direct synthesis of benzo[c]phenanthridines and benzo[c] phenanthridones via SRN1 reactions. J. Org. Chem. 1985, 50, 4933-4938.
-
(1985)
J. Org. Chem.
, vol.50
, pp. 4933-4938
-
-
Beugelmans, R.1
Chastanet, J.2
Ginsburg, H.3
Quintero-Cortes, L.4
Roussi, G.5
-
26
-
-
0032840102
-
Total synthesis of vancomycin: Part 1: design and development of methodology
-
(b) Nicolaou, K. C.; Li, H.; Boddy, C. N. C.; Ramanjulu, J. M.; Yue, T.-Y.; Natarajan, S.; Chu, X.-J.; Brase, S.; Rubsam, F. Total synthesis of vancomycin: Part 1: design and development of methodology. Chem. - Eur. J. 1999, 5, 2584-2601.
-
(1999)
Chem. - Eur. J.
, vol.5
, pp. 2584-2601
-
-
Nicolaou, K.C.1
Li, H.2
Boddy, C.N.C.3
Ramanjulu, J.M.4
Yue, T.-Y.5
Natarajan, S.6
Chu, X.-J.7
Brase, S.8
Rubsam, F.9
-
27
-
-
0038263126
-
Intramolecular conjuguate addition of alkenyl and aryl functions to enones initiated by lithium-iodine exchange
-
(c) Piers, E.; Harrison, C. L.; Zetina-Rocha, C. Intramolecular conjuguate addition of alkenyl and aryl functions to enones initiated by lithium-iodine exchange. Org. Lett. 2001, 3, 3245-3247.
-
(2001)
Org. Lett.
, vol.3
, pp. 3245-3247
-
-
Piers, E.1
Harrison, C.L.2
Zetina-Rocha, C.3
-
28
-
-
14844333286
-
An efficient entry to pyrrolo[1,2- B]isoquinolines and related systems through Parham cyclisation
-
(d) Ruiz, J.; Ardeo, A.; Ignacio, R.; Sotomayor, N.; Lete, E. An efficient entry to pyrrolo[1,2- b]isoquinolines and related systems through Parham cyclisation. Tetrahedron 2005, 61, 3311-3324.
-
(2005)
Tetrahedron
, vol.61
, pp. 3311-3324
-
-
Ruiz, J.1
Ardeo, A.2
Ignacio, R.3
Sotomayor, N.4
Lete, E.5
-
29
-
-
0036466841
-
Expression of a non-functional p53 affects the sensitivity of cancer cells to gemcitabine
-
DOI 10.1002/ijc.1628
-
Galmarini, C. M.; Clarke, M. L.; Falette, N.; Puisieux, A.; Mackey, J. R.; Dumontet, C. Expression of a non-functionnal P53 affects the sensitivity of cancer cells to gemcitabine. Int. J. Cancer 2002, 97, 439-445. (Pubitemid 34027801)
-
(2002)
International Journal of Cancer
, vol.97
, Issue.4
, pp. 439-445
-
-
Galmarini, C.M.1
Clarke, M.L.2
Falette, N.3
Puisieux, A.4
Mackey, J.R.5
Dumontet, C.6
-
30
-
-
0345393105
-
Purification of brain tubulin through two cycles of polymerization- depolymerization in a high-molarity buffer
-
Castoldi, M.; Popov, A. V. Purification of brain tubulin through two cycles of polymerization-depolymerization in a high-molarity buffer. Protein Expression Purif. 2003, 32, 83-88.
-
(2003)
Protein Expression Purif.
, vol.32
, pp. 83-88
-
-
Castoldi, M.1
Popov, A.V.2
-
31
-
-
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.; 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.
-
(2002)
Cancer Res.
, vol.62
, 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.9
Chaplin, D.J.10
Hill, S.A.11
-
32
-
-
33745231363
-
Identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines
-
Mulligan, J. M.; Greene, L. M.; Cloonan, S.; Mc Gee, M. M.; Onnis, V.; Campiani, G.; Fattorusso, C.; Lawler, M.; Williams, D. C.; Zisterer, D. M. Identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines. Mol. Pharmacol. 2006, 70, 60-70.
-
(2006)
Mol. Pharmacol.
, vol.70
, pp. 60-70
-
-
Mulligan, J.M.1
Greene, L.M.2
Cloonan, S.3
Mc Gee, M.M.4
Onnis, V.5
Campiani, G.6
Fattorusso, C.7
Lawler, M.8
Williams, D.C.9
Zisterer, D.M.10
-
33
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein- dye binding
-
Bradford, M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein- dye binding. Anal. Biochem. 1976, 72, 248-254.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
|