-
1
-
-
0033231927
-
The Aurora/Ipl1p kinase family: Regulators of chromosome segregation and cytokinesis
-
Bischoff, J. R.; Plowman, G. D. The Aurora/Ipl1p kinase family: regulators of chromosome segregation and cytokinesis. Trends Cell Biol. 1999, 9, 454-459.
-
(1999)
Trends Cell Biol.
, vol.9
, pp. 454-459
-
-
Bischoff, J.R.1
Plowman, G.D.2
-
2
-
-
0032100685
-
A homologue of Drosophila Aurora kinase is oncogenic and amplified in colorectal cancers
-
Bischoff, J. R.; Anderson, L.; Zhu, Y.; Mossie, K.; Ng, L.; Souza, B.; Schryver, B.; Flanagan, P.; Clairvoyant, F.; Ginther, C.; Chan, C. S. M.; Novotny, M.; Salomon, D. J.; Plowman, G. D. A homologue of Drosophila Aurora kinase is oncogenic and amplified in colorectal cancers. EMBO J. 1998, 17, 3052-3065.
-
(1998)
EMBO J.
, vol.17
, pp. 3052-3065
-
-
Bischoff, J.R.1
Anderson, L.2
Zhu, Y.3
Mossie, K.4
Ng, L.5
Souza, B.6
Schryver, B.7
Flanagan, P.8
Clairvoyant, F.9
Ginther, C.10
Chan, C.S.M.11
Novotny, M.12
Salomon, D.J.13
Plowman, G.D.14
-
3
-
-
0031714080
-
Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation
-
Zhou, H.; Kuang, J.; Zhong, L.; Kuo, W. L.; Gray, J. W.; Sahin, A.; Brinkley, B. R.; Sen, S. Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation. Nat. Genet. 1998, 20, 189-193.
-
(1998)
Nat. Genet.
, vol.20
, pp. 189-193
-
-
Zhou, H.1
Kuang, J.2
Zhong, L.3
Kuo, W.L.4
Gray, J.W.5
Sahin, A.6
Brinkley, B.R.7
Sen, S.8
-
5
-
-
0037018843
-
The kinase activity of Aurora B is required for kinetochore-microtubule interactions in mitosis
-
Murata-Hori, M.; Wang, Y. The kinase activity of Aurora B is required for kinetochore-microtubule interactions in mitosis. Curr. Biol. 2002, 12, 894-899.
-
(2002)
Curr. Biol.
, vol.12
, pp. 894-899
-
-
Murata-Hori, M.1
Wang, Y.2
-
6
-
-
0035858865
-
Essential role of Drosophila inner centromere protein (INCENP) and Aurora B in histone H3 phosphorylation, metaphase chromosome alignment, kinetochore disjunction, and chromosome segregation
-
Adams, R. R.; Maiato, H.; Earnshaw, W. C.; Carmena, M. Essential role of Drosophila inner centromere protein (INCENP) and Aurora B in histone H3 phosphorylation, metaphase chromosome alignment, kinetochore disjunction, and chromosome segregation. J. Cell. Biol. 2001, 153, 865-880.
-
(2001)
J. Cell. Biol.
, vol.153
, pp. 865-880
-
-
Adams, R.R.1
Maiato, H.2
Earnshaw, W.C.3
Carmena, M.4
-
7
-
-
0035577762
-
The budding yeast protein kinase Ipl1/Aurora allows the absence of tension to activate the spindle checkpoint
-
Biggins, S.; Murray, A. W. The budding yeast protein kinase Ipl1/Aurora allows the absence of tension to activate the spindle checkpoint. Genes Dev. 2001, 15, 3118-3129.
-
(2001)
Genes Dev.
, vol.15
, pp. 3118-3129
-
-
Biggins, S.1
Murray, A.W.2
-
8
-
-
0013057087
-
Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores
-
Dietchfield, C.; Johnson, V. L.; Tighe, A.; Ellston, R.; Haworth, C.; Johnson, T.; Mortlock, A.; Keen, N.; Taylor, S. S. Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores. J. Cell. Biol. 2003, 161, 267-280.
-
(2003)
J. Cell. Biol.
, vol.161
, pp. 267-280
-
-
Dietchfield, C.1
Johnson, V.L.2
Tighe, A.3
Ellston, R.4
Haworth, C.5
Johnson, T.6
Mortlock, A.7
Keen, N.8
Taylor, S.S.9
-
9
-
-
0037008684
-
Phosphorylation of the carboxyl terminus of inner centromere protein (INCENP) by Aurora B kinase stimulates Aurora B kinase activity
-
Bishop, J. D.; Schumacher, J. M. Phosphorylation of the carboxyl terminus of inner centromere protein (INCENP) by Aurora B kinase stimulates Aurora B kinase activity. J. Biol. Chem. 2002, 277, 27577-27580.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 27577-27580
-
-
Bishop, J.D.1
Schumacher, J.M.2
-
10
-
-
0036178929
-
Evidence that Ipl1-Sli15 (Aurora kinase-INCENP) complexe promotes bi-orientation by altering kinetochore-spindle pole connections
-
Tanaka, T. U.; Rachidi, N.; Janke, C.; Pereira, G.; Glova, M.; Schiebel, E.; Stark, M. J. R.; Nasmyth, K. Evidence that Ipl1-Sli15 (Aurora kinase-INCENP) complexe promotes bi-orientation by altering kinetochore-spindle pole connections. Cell 2002, 108, 317-329.
-
(2002)
Cell
, vol.108
, pp. 317-329
-
-
Tanaka, T.U.1
Rachidi, N.2
Janke, C.3
Pereira, G.4
Glova, M.5
Schiebel, E.6
Stark, M.J.R.7
Nasmyth, K.8
-
11
-
-
0037023490
-
Integrating functions at the kinetochore
-
Shimoda, S. L.; Solomon, F. Integrating functions at the kinetochore. Cell 2002, 109, 9-12.
-
(2002)
Cell
, vol.109
, pp. 9-12
-
-
Shimoda, S.L.1
Solomon, F.2
-
12
-
-
0035810919
-
INCENP is required for proper targeting of Survivin to the centromeres and the anaphase spindle during mitosis
-
Wheatley, S. P.; Carvalho, A.; Vagnarelli, P.; Earnshaw, W. C. INCENP is required for proper targeting of Survivin to the centromeres and the anaphase spindle during mitosis. Curr. Biol. 2001, 11, 886-890.
-
(2001)
Curr. Biol.
, vol.11
, pp. 886-890
-
-
Wheatley, S.P.1
Carvalho, A.2
Vagnarelli, P.3
Earnshaw, W.C.4
-
13
-
-
0036732808
-
Aurora B Kinase exists in a complex with Survivin and INCENP and its kinase activity is stimulated by Survivin binding and phosphorylation
-
Bolton, M. A.; Lan, W.; Powers, S. E.; McCleland, M. L.; Kuang, J.; Stukenberg, P. T. Aurora B Kinase exists in a complex with Survivin and INCENP and its kinase activity is stimulated by Survivin binding and phosphorylation. Mol. Biol. Cell 2002, 13, 3064-3077.
-
(2002)
Mol. Biol. Cell
, vol.13
, pp. 3064-3077
-
-
Bolton, M.A.1
Lan, W.2
Powers, S.E.3
McCleland, M.L.4
Kuang, J.5
Stukenberg, P.T.6
-
14
-
-
0035252654
-
Chromosomal passengers and the (Aurora) ABCs of mitosis
-
Adams, R. R.; Carmena, M.; Earnshaw, W. C. Chromosomal passengers and the (Aurora) ABCs of mitosis. Trends Cell Biol. 2001, 11, 49-54.
-
(2001)
Trends Cell Biol.
, vol.11
, pp. 49-54
-
-
Adams, R.R.1
Carmena, M.2
Earnshaw, W.C.3
-
15
-
-
0037414775
-
Survivin enhances Aurora-B kinase activity and localizes Aurora-B in human cells
-
Chen, J.; Jin, S.; Tahir, S. K.; Zhang, H.; Liu, X.; Sarthy, A. V.; McGonigal, T. P.; Liu, Z.; Rosenberg, S. H.; Ng, S. C. Survivin enhances Aurora-B kinase activity and localizes Aurora-B in human cells. J. Biol. Chem. 2003, 278, 486.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 486
-
-
Chen, J.1
Jin, S.2
Tahir, S.K.3
Zhang, H.4
Liu, X.5
Sarthy, A.V.6
McGonigal, T.P.7
Liu, Z.8
Rosenberg, S.H.9
Ng, S.C.10
-
17
-
-
0037586498
-
Aurora-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to taxol
-
Anaud, S.; Penrhyn-Lowe, S.; Venkitaraman, A. R. Aurora-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to taxol. Cancer Cell 2003, 3, 51-62.
-
(2003)
Cancer Cell
, vol.3
, pp. 51-62
-
-
Anaud, S.1
Penrhyn-Lowe, S.2
Venkitaraman, A.R.3
-
18
-
-
0035524309
-
Chromosome segregation and cancer: Cutting through the mystery
-
Jallepalli, P. V.; Lengauer, C. Chromosome segregation and cancer: Cutting through the mystery. Nat. Rev. Cancer 2001, 1, 109-117.
-
(2001)
Nat. Rev. Cancer
, vol.1
, pp. 109-117
-
-
Jallepalli, P.V.1
Lengauer, C.2
-
19
-
-
0034604354
-
Mitotic phosphorylation of histone H3 is governed by Ipl1/Aurora kinase and Glc 7/PP1 phosphatase in budding yeasts and nematodes
-
Hsu, J. Y.; Sun, Z. W.; Li, X.; Reuben, M.; Tatchell, K.; Bishop, D. K.; Grushcow, J. M.; Brame, C. J.; Caldwell, J. A.; Hunt, D. F.; Lin, R.; Smith, M. M.; Allis, C. D. Mitotic phosphorylation of histone H3 is governed by Ipl1/Aurora kinase and Glc 7/PP1 phosphatase in budding yeasts and nematodes. Cell 2000, 102, 279-291.
-
(2000)
Cell
, vol.102
, pp. 279-291
-
-
Hsu, J.Y.1
Sun, Z.W.2
Li, X.3
Reuben, M.4
Tatchell, K.5
Bishop, D.K.6
Grushcow, J.M.7
Brame, C.J.8
Caldwell, J.A.9
Hunt, D.F.10
Lin, R.11
Smith, M.M.12
Allis, C.D.13
-
20
-
-
0035911159
-
Drosophila Aurora B kinase is required for histone H3 phosphorylation and condensin recruitment during chromosome condensation and to organize the central spindle during cytokinesis
-
Giet, R.; Glover, D. M. Drosophila Aurora B kinase is required for histone H3 phosphorylation and condensin recruitment during chromosome condensation and to organize the central spindle during cytokinesis. J. Cell. Biol. 2001, 152, 669-682.
-
(2001)
J. Cell. Biol.
, vol.152
, pp. 669-682
-
-
Giet, R.1
Glover, D.M.2
-
21
-
-
0036142218
-
Mitotic phosphorylation of histone H3: Spatio-temporal regulation by mamelian Aurora kinases
-
Crosio, C.; Fimia, G. M.; Loury, R.; Kimura, M.; Okano, Y.; Zhou, H.; Sen, S.; Allis, C. D.; Sassone-Corsi, P. Mitotic phosphorylation of histone H3: Spatio-temporal regulation by mamelian Aurora kinases. Mol. Cell. Biol. 2002, 22, 874-885.
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 874-885
-
-
Crosio, C.1
Fimia, G.M.2
Loury, R.3
Kimura, M.4
Okano, Y.5
Zhou, H.6
Sen, S.7
Allis, C.D.8
Sassone-Corsi, P.9
-
22
-
-
0032716628
-
Aurora/Ipl1p-related kinases, a new family of mitotic serine-threonine kinases
-
Giet, R.; Prigent, C. Aurora/Ipl1p-related kinases, a new family of mitotic serine-threonine kinases. J. Cell Sci. 1999, 112, 3591-3601.
-
(1999)
J. Cell Sci.
, vol.112
, pp. 3591-3601
-
-
Giet, R.1
Prigent, C.2
-
23
-
-
0032213515
-
Multinuclearity and increased ploidy caused by overexpression of the Aurora-and Ipl1-like midbody-associated protein mitotic kinase in human cancer cells
-
Tatsuka, M.; Katayama, H.; Ota, T.; Tanaka, T.; Odashima, S.; Suzuki, F.; Terada, Y. Multinuclearity and increased ploidy caused by overexpression of the Aurora-and Ipl1-like midbody-associated protein mitotic kinase in human cancer cells. Cancer Res. 1998, 58, 4811-4816.
-
(1998)
Cancer Res.
, vol.58
, pp. 4811-4816
-
-
Tatsuka, M.1
Katayama, H.2
Ota, T.3
Tanaka, T.4
Odashima, S.5
Suzuki, F.6
Terada, Y.7
-
24
-
-
2342639645
-
VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumour growth in vivo
-
Harrington, E. A.; Bebbington, D.; Moore, J.; Rasmussen, R. K.; Ajose-Adeogun, A. O.; Nakayama, T.; Graham, J. A.; Demur, C.; Hercend, T.; Diu-Hercend, A.; Su, M.; Golec, J. M. C.; Miller, K. M. VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumour growth in vivo. Nat. Med. 2004, 10, 262-267.
-
(2004)
Nat. Med.
, vol.10
, pp. 262-267
-
-
Harrington, E.A.1
Bebbington, D.2
Moore, J.3
Rasmussen, R.K.4
Ajose-Adeogun, A.O.5
Nakayama, T.6
Graham, J.A.7
Demur, C.8
Hercend, T.9
Diu-Hercend, A.10
Su, M.11
Golec, J.M.C.12
Miller, K.M.13
-
25
-
-
0038746733
-
The small molecule Hesperadin reveals a role for Aurora B in connecting kinetochore-microtubule attachement and in maintaining the spindle assembly checkpoint
-
Hauf, S.; Cole, R. W.; LaTerra, S.; Zimmer, C.; Schnapp, G.; Walter, R.; Heckel, A.; Van Meel, J.; Rieder, C. L.; Peters, J.-M. The small molecule Hesperadin reveals a role for Aurora B in connecting kinetochore-microtubule attachement and in maintaining the spindle assembly checkpoint. J. Cell Biol. 2003, 161, 281-294.
-
(2003)
J. Cell Biol.
, vol.161
, pp. 281-294
-
-
Hauf, S.1
Cole, R.W.2
Laterra, S.3
Zimmer, C.4
Schnapp, G.5
Walter, R.6
Heckel, A.7
Van Meel, J.8
Rieder, C.L.9
Peters, J.-M.10
-
26
-
-
0029130763
-
Tyrosine kinase inhibitors. Synthesis and structure-activity relationships for 4-[(phenylmethyl)amino]- And 4-(phenylamino)quinazolines as potent adenosine 5′-triphosphate binding site inhibitors of the tyrosine kinase domaine of the epidermal growth factor receptor
-
Rewcastle, G. W.; Denny, W. A.; Bridges, A. J.; Zhou, H.; Cody, D. R.; McMichael, A.; Fry, D. W. Tyrosine kinase inhibitors. Synthesis and structure-activity relationships for 4-[(phenylmethyl)amino]- and 4-(phenylamino)quinazolines as potent adenosine 5′-triphosphate binding site inhibitors of the tyrosine kinase domaine of the epidermal growth factor receptor. J. Med. Chem. 1995, 38, 3482-3487.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3482-3487
-
-
Rewcastle, G.W.1
Denny, W.A.2
Bridges, A.J.3
Zhou, H.4
Cody, D.R.5
McMichael, A.6
Fry, D.W.7
-
27
-
-
0035899182
-
6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumour activity
-
Tsou, H.-R.; Mamuya, N.; Johnson, B. D.; Reich, M. F.; Gruber, B. C.; Ye, F.; Nilakanatan, R.; Shen, R.; Discafani, C.; DeBlanc, R.; Davis, R.; Koehn, F. E.; Greenberger, L. M.; Wang, Y.-F.; Wissner, A. 6-substituted-4-(3- bromophenylamino)quinazolines as putative irreversible inhibitors of epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumour activity. J. Med. Chem. 2001, 44, 2719-2734.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2719-2734
-
-
Tsou, H.-R.1
Mamuya, N.2
Johnson, B.D.3
Reich, M.F.4
Gruber, B.C.5
Ye, F.6
Nilakanatan, R.7
Shen, R.8
Discafani, C.9
Deblanc, R.10
Davis, R.11
Koehn, F.E.12
Greenberger, L.M.13
Wang, Y.-F.14
Wissner, A.15
-
28
-
-
9844235351
-
Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(Phenylamino)pyrazolo[3,4-d]pyrimidines
-
Traxler, P.; Bold, G.; Frei, J.; Lang, M.; Lydon, N.; Mett, H.; Buchdunger, E.; Meyer, T.; Mueller, M.; Furet, P. Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(Phenylamino)pyrazolo[3,4- d]pyrimidines. J. Med. Chem. 1997, 40, 3601-3616.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3601-3616
-
-
Traxler, P.1
Bold, G.2
Frei, J.3
Lang, M.4
Lydon, N.5
Mett, H.6
Buchdunger, E.7
Meyer, T.8
Mueller, M.9
Furet, P.10
-
29
-
-
32344450624
-
-
Preparation of substituted quinazoline derivatives and their use as inhibitors of Aurora-2 kinase. WO 2002000649 A1 20020103. CAN 136:85826
-
Mortlock, A. A.; Jung, F. H. Preparation of substituted quinazoline derivatives and their use as inhibitors of Aurora-2 kinase. WO 2002000649 A1 20020103. CAN 136:85826.
-
-
-
Mortlock, A.A.1
Jung, F.H.2
-
30
-
-
32344442080
-
-
Preparation of substituted quinazoline derivatives as inhibitors of Aurora kinases. WO 2003055491 A1 20030710. CAN 139:101142
-
Jung, F. H.; Pasquet, G. R. Preparation of substituted quinazoline derivatives as inhibitors of Aurora kinases. WO 2003055491 A1 20030710. CAN 139:101142.
-
-
-
Jung, F.H.1
Pasquet, G.R.2
-
31
-
-
23944488863
-
Progress in the Development of Selective Inhibitors of Aurora kinases
-
Mortlock, A. A.; Keen, N. J.; Jung, F. H.; Heron, N. M.; Foote, K. M.; Wilkinson, R.; Green, S. Progress in the Development of Selective Inhibitors of Aurora kinases. Curr. Top. Med. Chem. 2005, 5, 199-213.
-
(2005)
Curr. Top. Med. Chem.
, vol.5
, pp. 199-213
-
-
Mortlock, A.A.1
Keen, N.J.2
Jung, F.H.3
Heron, N.M.4
Foote, K.M.5
Wilkinson, R.6
Green, S.7
-
32
-
-
31344438721
-
SAR and inhibitor complex structure determination of a novel class of potent and specific Aurora kinase inhibitors
-
In press
-
Heron, N. M.; Anderson, M.; Blowers, D. P.; Breed, J.; Eden, J. M.; Green, S.; Hill, G. B.; Johnson, T.; Jung, F. H.; McMiken, H. H. J.; Mortlock, A. A.; Pannifer, A. D.; Pauptit, R. A.; Pink, J.; Roberts, N. J.; Rowsell, S. SAR and Inhibitor Complex Structure Determination of a Novel Class of Potent and Specific Aurora Kinase Inhibitors. Bioorg. Med. Chem. Lett. In press.
-
Bioorg. Med. Chem. Lett.
-
-
Heron, N.M.1
Anderson, M.2
Blowers, D.P.3
Breed, J.4
Eden, J.M.5
Green, S.6
Hill, G.B.7
Johnson, T.8
Jung, F.H.9
McMiken, H.H.J.10
Mortlock, A.A.11
Pannifer, A.D.12
Pauptit, R.A.13
Pink, J.14
Roberts, N.J.15
Rowsell, S.16
-
33
-
-
0004133516
-
-
Gaussian, Inc.: Pittsburgh, PA
-
Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Zakrzewski, V. G.; Montgomery, J. A., Jr.; Stratmann, R. E.; Burant, J. C.; Dapprich, S.; Millam, J. M.; Daniels, A. D.; Kudin, K. N.; Strain, M. C.; Farkas, O.; Tomasi, J.; Barone, V.; Cossi, M.; Cammi, R.; Mennucci, B.; Pomelli, C.; Adamo, C.; Clifford, S.; Ochterski, J.; Petersson, G. A.; Ayala, P. Y.; Cui, Q.; Morokuma, K.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Cioslowski, J.; Ortiz, J. V.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Gonzalez, C.; Challacombe, M.; Gill, P. M. W.; Johnson, B. G.; Chen, W.; Wong, M. W.; Andres, J. L.; Head-Gordon, M.; Replogle, E. S.; Pople, J. A. Gaussian 98, revision A. 11.3; Gaussian, Inc.: Pittsburgh, PA, 2002.
-
(2002)
Gaussian 98, Revision A. 11.3
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Zakrzewski, V.G.7
Montgomery Jr., J.A.8
Stratmann, R.E.9
Burant, J.C.10
Dapprich, S.11
Millam, J.M.12
Daniels, A.D.13
Kudin, K.N.14
Strain, M.C.15
Farkas, O.16
Tomasi, J.17
Barone, V.18
Cossi, M.19
Cammi, R.20
Mennucci, B.21
Pomelli, C.22
Adamo, C.23
Clifford, S.24
Ochterski, J.25
Petersson, G.A.26
Ayala, P.Y.27
Cui, Q.28
Morokuma, K.29
Malick, D.K.30
Rabuck, A.D.31
Raghavachari, K.32
Foresman, J.B.33
Cioslowski, J.34
Ortiz, J.V.35
Stefanov, B.B.36
Liu, G.37
Liashenko, A.38
Piskorz, P.39
Komaromi, I.40
Gomperts, R.41
Martin, R.L.42
Fox, D.J.43
Keith, T.44
Al-Laham, M.A.45
Peng, C.Y.46
Nanayakkara, A.47
Gonzalez, C.48
Challacombe, M.49
Gill, P.M.W.50
Johnson, B.G.51
Chen, W.52
Wong, M.W.53
Andres, J.L.54
Head-Gordon, M.55
Replogle, E.S.56
Pople, J.A.57
more..
-
34
-
-
13944252481
-
CH...O and CH...N hydrogen bonds in ligand design: A Novel quinazolin-4-ylthiazol-2-ylamine protein kinase inhibitor
-
Pierce, A. C.; ter Haar, E.; Binch, H. M.; Kay, D. P.; Patel, S. R.; Li, P. CH...O and CH...N Hydrogen Bonds in Ligand Design: A Novel Quinazolin-4-ylthiazol-2-ylamine Protein Kinase Inhibitor. J. Med. Chem. 2005, 48, 1278-81.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1278-1281
-
-
Pierce, A.C.1
Ter Haar, E.2
Binch, H.M.3
Kay, D.P.4
Patel, S.R.5
Li, P.6
-
35
-
-
0242330123
-
Structural basis of Aurora-A activation by TPX2 at the mitotic spindle
-
Bayliss, R.; Sardon, T.; Vernos, I.; Conti, E. Structural basis of Aurora-A activation by TPX2 at the mitotic spindle. Mol. Cell. 2003, 12, 851-862.
-
(2003)
Mol. Cell.
, vol.12
, pp. 851-862
-
-
Bayliss, R.1
Sardon, T.2
Vernos, I.3
Conti, E.4
-
36
-
-
1842848073
-
Structures of the cancer-related aurora-A, FAK, and EphA2 protein kinases from nanovolume crystallography
-
Nowakowski, J.; Cronin, C. N.; McRee, D. E.; Knuth, M. W.; Nelson, C. G.; Pavletich, N. P.; Rogers, J.; Sang, B. C.; Scheibe, D. N.; Swanson, R. V.; Thompson, D. A. Structures of the cancer-related aurora-A, FAK, and EphA2 protein kinases from nanovolume crystallography. Structure 2002, 10, 1659-1667.
-
(2002)
Structure
, vol.10
, pp. 1659-1667
-
-
Nowakowski, J.1
Cronin, C.N.2
McRee, D.E.3
Knuth, M.W.4
Nelson, C.G.5
Pavletich, N.P.6
Rogers, J.7
Sang, B.C.8
Scheibe, D.N.9
Swanson, R.V.10
Thompson, D.A.11
-
37
-
-
0037044846
-
Crystal structure of aurora-2, an oncogenic serine/threonine kinase
-
Cheetham, G. M. T.; Knegtel, R. M. A.; Coll, J. T.; Renwick, S. B.; Swenson, L.; Weber, P.; Lippke, J. A.; Austen, D. A. Crystal structure of aurora-2, an oncogenic serine/threonine kinase. J. Biol. Chem. 2002, 277, 42419-42422.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 42419-42422
-
-
Cheetham, G.M.T.1
Knegtel, R.M.A.2
Coll, J.T.3
Renwick, S.B.4
Swenson, L.5
Weber, P.6
Lippke, J.A.7
Austen, D.A.8
-
38
-
-
0036682301
-
Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571)
-
Nagar, B.; Bornmann, W. G.; Pellicena, P.; Schindler, T.; Veach, D. R.; Miller, W. T.; Clarkson, B.; Kuriyan, J. Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571). Cancer Res. 2002, 62, 4236-4243.
-
(2002)
Cancer Res.
, vol.62
, pp. 4236-4243
-
-
Nagar, B.1
Bornmann, W.G.2
Pellicena, P.3
Schindler, T.4
Veach, D.R.5
Miller, W.T.6
Clarkson, B.7
Kuriyan, J.8
-
39
-
-
18344395134
-
Inhibition of P38 MAP kinase by utilizing a novel allosteric binding site
-
Pargellis, C.; Tong, L.; Churchill, L.; Cirillo, P. F.; Gilmore, T.; Graham, A. G.; Grob, P. M.; Hickey, E. R.; Moss, N.; Pav, S.; Regan, J. Inhibition of P38 MAP kinase by utilizing a novel allosteric binding site. Nat. Struct. Biol. 2002, 9, 268-272.
-
(2002)
Nat. Struct. Biol.
, vol.9
, pp. 268-272
-
-
Pargellis, C.1
Tong, L.2
Churchill, L.3
Cirillo, P.F.4
Gilmore, T.5
Graham, A.G.6
Grob, P.M.7
Hickey, E.R.8
Moss, N.9
Pav, S.10
Regan, J.11
-
40
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
Wan, P. T. C.; Garnett, M. J.; Roe, S. M.; Lee, S.; Niculescu-Duvaz, D.; Good, V. M.; Cancer Genome Project; Jones, C. M.; Marshall, C. J.; Springer, C. J.; Barford, D.; Marais, R. Mechanism of Activation of the RAF-ERK Signaling Pathway by Oncogenic Mutations of B-RAF. Cell. 2004, 116 (6), 855-67.
-
(2004)
Cell.
, vol.116
, Issue.6
, pp. 855-867
-
-
Wan, P.T.C.1
Garnett, M.J.2
Roe, S.M.3
Lee, S.4
Niculescu-Duvaz, D.5
Good, V.M.6
Jones, C.M.7
Marshall, C.J.8
Springer, C.J.9
Barford, D.10
Marais, R.11
-
41
-
-
20844436307
-
Mechanism of Aurora B activation by INCENP and inhibition by hesperadin
-
Sessa, F.; Mapelli, M.; Ciferri, C.; Tarricone, C.; Araces, L. B.; Schneider, T. R.; Stukenberg, P. T.; Musacchio, A. Mechanism of Aurora B Activation by INCENP and Inhibition by Hesperadin. Cell. 2005, 18 (3), 379-91.
-
(2005)
Cell.
, vol.18
, Issue.3
, pp. 379-391
-
-
Sessa, F.1
Mapelli, M.2
Ciferri, C.3
Tarricone, C.4
Araces, L.B.5
Schneider, T.R.6
Stukenberg, P.T.7
Musacchio, A.8
-
42
-
-
17544387877
-
Design and structure-activity relationship of a new class of potent VEGF receptor tyrosine kinase inhibitors
-
Hennequin, L. F.; Thomas, A. P.; Johnstone, C.; Stokes, E. S. E.; Plé, P. A.; Lohmann, J. J. M.; Ogilvie, D. J.; Dukes, M.; Wedge, S. R.; Curven, J. O.; Kendrew, J.; Lambert-van der Brempt, C. Design and structure-activity relationship of a new class of potent VEGF receptor tyrosine kinase inhibitors. J. Med. Chem. 1999, 42, 5369-5389.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 5369-5389
-
-
Hennequin, L.F.1
Thomas, A.P.2
Johnstone, C.3
Stokes, E.S.E.4
Plé, P.A.5
Lohmann, J.J.M.6
Ogilvie, D.J.7
Dukes, M.8
Wedge, S.R.9
Curven, J.O.10
Kendrew, J.11
Lambert-Van Der Brempt, C.12
-
43
-
-
0037075812
-
Novel 4-anilinoquinazolines with C7 basic side chains: Design and structure activity relationship of a series of potent, orally active, VEGF receptor tyrosine kinase inhibitors
-
Hennequin, L. F.; Stokes, E. S. E.; Thomas, A. P.; Johnstone, C.; Plé, P. A.; Ogilvie, D. J.; Dukes, M.; Wedge, S. R.; Kendrew, J.; Curven, J. O. Novel 4-anilinoquinazolines with C7 basic side chains: Design and structure activity relationship of a series of potent, orally active, VEGF receptor tyrosine kinase inhibitors. J. Med. Chem. 2002, 45, 1300-1312.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1300-1312
-
-
Hennequin, L.F.1
Stokes, E.S.E.2
Thomas, A.P.3
Johnstone, C.4
Plé, P.A.5
Ogilvie, D.J.6
Dukes, M.7
Wedge, S.R.8
Kendrew, J.9
Curven, J.O.10
-
44
-
-
0037103166
-
Identification of orally active, potent and selective 4-piperazinylquinazolines as antagonists of the platelet-derived growth factor receptor tyrosine kinase family
-
Pandey, A.; Volkots, D. L.; Seroogy, J. M.; Rose, J. W.; Yu, J. C.; Lambing, J. L.; Hutchaleelaka, A.; Hollenbach, S. J.; Abe, K.; Giese, N. A.; Scarborough, R. M. Identification of orally active, potent and selective 4-piperazinylquinazolines as antagonists of the platelet-derived growth factor receptor tyrosine kinase family. J. Med. Chem. 2002, 45, 3772-3793.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3772-3793
-
-
Pandey, A.1
Volkots, D.L.2
Seroogy, J.M.3
Rose, J.W.4
Yu, J.C.5
Lambing, J.L.6
Hutchaleelaka, A.7
Hollenbach, S.J.8
Abe, K.9
Giese, N.A.10
Scarborough, R.M.11
-
45
-
-
0034611617
-
Tyrosine kinase inhibitors. 17. Irreversible inhibitors of epidermal growth factor receptor. 4-(Phenylamino)quinazoline- and 4-(phenylamino)pyrido[3, 2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions
-
Smaill, J. B.; Rewcastle, G. W.; Loo, J. A.; Greis, K. D.; Chan, O. H.; Reyner, E. L.; Lipka, E.; Showalter, H. D. H.; Vincent, P. W.; Elliot, W. L.; Denny, W. A. Tyrosine kinase inhibitors. 17. Irreversible inhibitors of epidermal growth factor receptor. 4-(Phenylamino)quinazoline- and 4-(phenylamino)pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions. J. Med. Chem. 2000, 43, 1380-1397.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1380-1397
-
-
Smaill, J.B.1
Rewcastle, G.W.2
Loo, J.A.3
Greis, K.D.4
Chan, O.H.5
Reyner, E.L.6
Lipka, E.7
Showalter, H.D.H.8
Vincent, P.W.9
Elliot, W.L.10
Denny, W.A.11
-
46
-
-
27944442202
-
Zur synthese von 2-aminothiazolderivaten
-
Erlenmeyer, H.; Herzfeld, L.; Prijs, B. Zur synthese von 2-aminothiazolderivaten. Helv. Chem. Acta 1955, 38, 1291-1294.
-
(1955)
Helv. Chem. Acta
, vol.38
, pp. 1291-1294
-
-
Erlenmeyer, H.1
Herzfeld, L.2
Prijs, B.3
-
47
-
-
0030444537
-
Iminophosphorane-mediated synthesis of 2-aminoimidazole derivatives
-
Molina, P.; Conesa, C.; Velasco, M. D. Iminophosphorane-mediated synthesis of 2-aminoimidazole derivatives. Synthesis 1996, 1459-1462.
-
(1996)
Synthesis
, pp. 1459-1462
-
-
Molina, P.1
Conesa, C.2
Velasco, M.D.3
-
48
-
-
0000980004
-
Studies in the azole series
-
Gompper, R.; Christmann, O. Studies in the azole series. Chem. Ber. 1959, 92, 1944-1949.
-
(1959)
Chem. Ber.
, vol.92
, pp. 1944-1949
-
-
Gompper, R.1
Christmann, O.2
-
49
-
-
2842561500
-
Synthesis of substituted 4H-thiazolo[4,5-b][1]benzothiopyran-4-ones as possible schistosomicidal agents
-
El-Kerdawy, M. M.; El-Emam, A. A.; El-Subbagh, H. I.; Abushanab, E. Synthesis of substituted 4H-thiazolo[4,5-b][1]benzothiopyran-4-ones as possible schistosomicidal agents. Monatsch. Chem. 1989, 120, 991-995.
-
(1989)
Monatsch. Chem.
, vol.120
, pp. 991-995
-
-
El-Kerdawy, M.M.1
El-Emam, A.A.2
El-Subbagh, H.I.3
Abushanab, E.4
-
50
-
-
32344453176
-
A facile nucleophilic displacement of bromine in 2-amino-4-methyl-5- bromothiazole by a thiophenoxide anion
-
Mahajanshetti, C. S.; Basanagoudar, L. D. A facile nucleophilic displacement of bromine in 2-amino-4-methyl-5-bromothiazole by a thiophenoxide anion. Can. J. Chem. 1967, 45, 1807-1810.
-
(1967)
Can. J. Chem.
, vol.45
, pp. 1807-1810
-
-
Mahajanshetti, C.S.1
Basanagoudar, L.D.2
-
51
-
-
32344442326
-
-
Preparation of dicyanopyridine derivatives as high-conductance calcium-sensitive potassium channel openers. WO 20026237 A1 20020124. CAN 136:118474
-
Harada, H.; Watanuki, S.; Takuwa, T.; Kawaguchi, K.; Okazaki, T.; Hirano, Y.; Saitoh, C. Preparation of dicyanopyridine derivatives as high-conductance calcium-sensitive potassium channel openers. WO 20026237 A1 20020124. CAN 136:118474.
-
-
-
Harada, H.1
Watanuki, S.2
Takuwa, T.3
Kawaguchi, K.4
Okazaki, T.5
Hirano, Y.6
Saitoh, C.7
-
52
-
-
0034652716
-
ZD4190: An orally active inhibitor of vascular endothelial growth factor signaling with broad-spectrum antitumor efficacy
-
Wedge, S. R.; Ogilvie, D. J.; Dukes, M.; Kendrew, J.; Curwen, J. O.; Hennequin, L. F.; Thomas, A. P.; Stokes, E. S. E.; Curry, B.; Richmond, G. H. P.; Wadsworth, P. F. ZD4190: An orally active inhibitor of vascular endothelial growth factor signaling with broad-spectrum antitumor efficacy. Cancer Res. 2000, 60, 970-975.
-
(2000)
Cancer Res.
, vol.60
, pp. 970-975
-
-
Wedge, S.R.1
Ogilvie, D.J.2
Dukes, M.3
Kendrew, J.4
Curwen, J.O.5
Hennequin, L.F.6
Thomas, A.P.7
Stokes, E.S.E.8
Curry, B.9
Richmond, G.H.P.10
Wadsworth, P.F.11
-
53
-
-
0348091307
-
-
Tripos Inc., St. Louis, MO
-
SYBYL 6.9.1; Tripos Inc., St. Louis, MO.
-
SYBYL 6.9.1
-
-
-
54
-
-
0004314831
-
-
A.; Semichem Inc.: Kansas City, MO
-
AMPAC, version 6.55 A.; Semichem Inc.: Kansas City, MO, 1999.
-
(1999)
AMPAC, Version 6.55
-
-
-
55
-
-
20944437351
-
Potent and selective aurora inhibitors identified by the expansion of a novel Scaffold for protein kinase inhibition
-
Fancelli, D.; Berta, D.; Bindi, S.; Cameron, A.; Cappella, O.; Carpinelli, P.; Catana, C.; Forte, B.; Giordano, P.; Giorgini, M. L.; Mantegani, S.; Marsiglio, A.; Meroni, M.; Moll, J.; Pittalà, V.; Roletto, F.; Severino, D.; Soncini, C.; Storici, P.; Tonani, R.; Varasi, M.; Vulpetti, A.; Vianello, P. Potent and Selective Aurora Inhibitors Identified by the Expansion of a Novel Scaffold for Protein Kinase Inhibition. J. Med. Chem. 2005, 48, 3080-3084.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 3080-3084
-
-
Fancelli, D.1
Berta, D.2
Bindi, S.3
Cameron, A.4
Cappella, O.5
Carpinelli, P.6
Catana, C.7
Forte, B.8
Giordano, P.9
Giorgini, M.L.10
Mantegani, S.11
Marsiglio, A.12
Meroni, M.13
Moll, J.14
Pittalà, V.15
Roletto, F.16
Severino, D.17
Soncini, C.18
Storici, P.19
Tonani, R.20
Varasi, M.21
Vulpetti, A.22
Vianello, P.23
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