-
1
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan, D.; Weinberg, R. A. The Hallmarks of Cancer. Cell 2000, 100, 57-70.
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
2
-
-
0035754080
-
To cycle or not to cycle: A critical decision in cancer
-
Malumbres, M.; Barbacid, M. To cycle or not to cycle: a critical decision in cancer. Nat. Rev. Cancer 2001, 1, 222-231.
-
(2001)
Nat. Rev. Cancer
, vol.1
, pp. 222-231
-
-
Malumbres, M.1
Barbacid, M.2
-
3
-
-
0029849620
-
Cancer cell cycles
-
Sherr, C. J. Cancer Cell Cycles. Science 1996, 274, 1672-1677.
-
(1996)
Science
, vol.274
, pp. 1672-1677
-
-
Sherr, C.J.1
-
4
-
-
0031466305
-
Cyclin-dependent kinases: Engines, clocks, and microprocessors
-
Morgan, D. O. Cyclin-dependent kinases: engines, clocks, and microprocessors. Annu. Rev. Cell. Dev. Biol. 1997, 13, 261-291.
-
(1997)
Annu. Rev. Cell. Dev. Biol.
, vol.13
, pp. 261-291
-
-
Morgan, D.O.1
-
5
-
-
0033564697
-
CDK inhibitors positive and negative regulators of G1-phase progression
-
Sherr, C. J.; Roberts, J. M. CDK Inhibitors: Positive and Negative Regulators of G1-Phase Progression. Genes Dev. 1999, 13, 1501-1512.
-
(1999)
Genes Dev.
, vol.13
, pp. 1501-1512
-
-
Sherr, C.J.1
Roberts, J.M.2
-
6
-
-
0034033642
-
Inhibitors of cyclin-dependent kinases as therapeutic agents for the treatment of cancer
-
Fry, D. W.; Garrett, M. D. Inhibitors of Cyclin-Dependent Kinases as Therapeutic Agents for the Treatment of Cancer. Curr. Opin. Oncologic, Endocrine Metab. Invest. Drugs. 2000, 2, 40-59.
-
(2000)
Curr. Opin. Oncologic, Endocrine Metab. Invest. Drugs
, vol.2
, pp. 40-59
-
-
Fry, D.W.1
Garrett, M.D.2
-
8
-
-
0038685911
-
CDK inhibitors in clinical development for the treatment of cancer
-
Fisher, P. M.; Gianella-Borradori, A. CDK Inhibitors in Clinical Development for the Treatment of Cancer. Expert. Opin. Investig. Drugs 2003, 12, 955-970.
-
(2003)
Expert. Opin. Investig. Drugs
, vol.12
, pp. 955-970
-
-
Fisher, P.M.1
Gianella-Borradori, A.2
-
9
-
-
0038245253
-
Small molecules as inhibitors of cyclin-dependent kinases
-
Huwe, A.; Mazitschek, R.; Giannis, A. Small Molecules as Inhibitors of Cyclin-Dependent Kinases. Angew. Chem. Int. Ed. 2003, 42, 2122-2138.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2122-2138
-
-
Huwe, A.1
Mazitschek, R.2
Giannis, A.3
-
10
-
-
0034807335
-
Recent advances and new directions in the discovery and development of cyclin-dependent kinase inhibitors
-
Fisher, P. M. Recent Advances and New Directions in the Discovery and Development of Cyclin-Dependent Kinase Inhibitors. Curr. Opin. Drug Discuss. Dev. 2001, 4, 623-634.
-
(2001)
Curr. Opin. Drug Discuss. Dev.
, vol.4
, pp. 623-634
-
-
Fisher, P.M.1
-
11
-
-
0033957960
-
Targeting hyperproliferative disorders with cyclin dependent kinase inhibitors
-
Rosania, G. R.; Chang, Y.-T. Targeting Hyperproliferative Disorders with Cyclin Dependent Kinase Inhibitors. Exp. Opin. Ther. Pat. 2000, 10, 215-230.
-
(2000)
Exp. Opin. Ther. Pat.
, vol.10
, pp. 215-230
-
-
Rosania, G.R.1
Chang, Y.-T.2
-
12
-
-
0033995530
-
Novel drugs targeting the cell cycle
-
Webster, K. R.; Kimball, S. D. Novel Drugs Targeting the Cell Cycle. Emerging Drugs 2000, 5, 45-59.
-
(2000)
Emerging Drugs
, vol.5
, pp. 45-59
-
-
Webster, K.R.1
Kimball, S.D.2
-
13
-
-
0034642532
-
Cyclin-dependent kinase inhibitors: Useful targets in cell cycle regulation
-
Sielecki, T. M.; Boylan, J. F.; Benfield, P. A.; Trainor, G. L. Cyclin-Dependent Kinase Inhibitors: Useful Targets in Cell Cycle Regulation. J. Med. Chem. 2000, 43, 1-18.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1-18
-
-
Sielecki, T.M.1
Boylan, J.F.2
Benfield, P.A.3
Trainor, G.L.4
-
14
-
-
0033900827
-
Cyclin-dependent kinase inhibitors; novel anticancer agents
-
Mani, S.; Wang, C.; Wu, K.; Francis, R.; Pestell, R. Cyclin-Dependent Kinase Inhibitors; Novel Anticancer Agents. Exp. Opin. Invest. Drugs 2000, 9, 1849-1870.
-
(2000)
Exp. Opin. Invest. Drugs
, vol.9
, pp. 1849-1870
-
-
Mani, S.1
Wang, C.2
Wu, K.3
Francis, R.4
Pestell, R.5
-
15
-
-
0037665145
-
Roscovitine and other purines as kinase inhibitors. From starfish oocytes to clinical trials
-
Meijer, L. Roscovitine and other purines as kinase inhibitors. From starfish Oocytes to Clinical trials. Acc. Chem. Res, 2003, 36, 417-425.
-
(2003)
Acc. Chem. Res.
, vol.36
, pp. 417-425
-
-
Meijer, L.1
-
16
-
-
0036785882
-
Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor
-
Davies, T. G.; Bentley, J.; Arris, C. E.; Boyle, F. T.; Curtin, N, J.; Endicott, J, A.; Gibson, A. E.; Golding, B. T.; Griffin, R. J.; Hardcastle, I. R.; Jewsbury, P.; Johnson, L. N.; Mesguiche, V.; Newell, D. R.; Noble, M. E. M.; Tucker, J. A.; Wang, L.; Whitfield, H. J. Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor. Nat. Struct. Biol. 2002, 9, 745-749.
-
(2002)
Nat. Struct. Biol.
, vol.9
, pp. 745-749
-
-
Davies, T.G.1
Bentley, J.2
Arris, C.E.3
Boyle, F.T.4
Curtin, N.J.5
Endicott, J.A.6
Gibson, A.E.7
Golding, B.T.8
Griffin, R.J.9
Hardcastle, I.R.10
Jewsbury, P.11
Johnson, L.N.12
Mesguiche, V.13
Newell, D.R.14
Noble, M.E.M.15
Tucker, J.A.16
Wang, L.17
Whitfield, H.J.18
-
17
-
-
0035865934
-
Crystal structure of human cyclin-dependent kinase 2 in complex with the adenine-derived inhibitor H717
-
Dreyer, M. K.; Borcherding, D. R.; Dumont, J. A.; Peet, N. P.; Tsay, J. T.; Wright, P. S.; Bitonti, A. J.; Shen, J.; Kim, S.-H. Crystal Structure of Human Cyclin-Dependent Kinase 2 in Complex with the Adenine-Derived Inhibitor H717. J. Med. Chem. 2001, 44, 524-530.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 524-530
-
-
Dreyer, M.K.1
Borcherding, D.R.2
Dumont, J.A.3
Peet, N.P.4
Tsay, J.T.5
Wright, P.S.6
Bitonti, A.J.7
Shen, J.8
Kim, S.-H.9
-
18
-
-
0034611620
-
Cyclin-dependent kinase inhibition by New C-2 alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex
-
Legraverend, M.; Tunnah, P.; Noble, M.; Ducrot, P.; Ludwig, O.; Grierson, D. S.; Leost, M.; Meijer, L.; Endicott, J. Cyclin-Dependent Kinase Inhibition by New C-2 Alkynylated Purine Derivatives and Molecular Structure of a CDK2-Inhibitor Complex. J. Med. Chem. 2000, 43, 1282-1292.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1282-1292
-
-
Legraverend, M.1
Tunnah, P.2
Noble, M.3
Ducrot, P.4
Ludwig, O.5
Grierson, D.S.6
Leost, M.7
Meijer, L.8
Endicott, J.9
-
19
-
-
0035856638
-
Synthesis and configuration of the cyclin-dependent kinase inhibitor roscovitine and its enantiomer
-
Wang, S.; McClue, S. J.; Ferguson, J. R.; Hull, J. D.; Stokes, S.; Parsons, S.; Westwood, R.; Fischer, P. M. Synthesis and configuration of the cyclin-dependent kinase inhibitor roscovitine and its enantiomer. Tetrahedron: Asymmetry 2001, 12, 2891-2894.
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 2891-2894
-
-
Wang, S.1
McClue, S.J.2
Ferguson, J.R.3
Hull, J.D.4
Stokes, S.5
Parsons, S.6
Westwood, R.7
Fischer, P.M.8
-
20
-
-
0033150476
-
Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors
-
Chang, Y.-T.; Gray, N. S.; Rosania, G. R.; Sutherlin, D. P.; Kwon, S.; Norman, T. C.; Sarohia, R.; Leost, M.; Meijer, L.; Schultz, P. G. Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors. Chem. Biol. 1999, 6, 361-375.
-
(1999)
Chem. Biol.
, vol.6
, pp. 361-375
-
-
Chang, Y.-T.1
Gray, N.S.2
Rosania, G.R.3
Sutherlin, D.P.4
Kwon, S.5
Norman, T.C.6
Sarohia, R.7
Leost, M.8
Meijer, L.9
Schultz, P.G.10
-
21
-
-
0032918488
-
2,6,9-Trisubstituted purines: Optimization towards highly potent and selective CDK1 inhibitors
-
Imbach, P.; Capraro, H.-G.; Furet, P.; Mett, H.; Meyer, T.; Zimmermann, J. 2,6,9-Trisubstituted Purines: Optimization towards highly potent and selective CDK1 inhibitors. Bioorg. Med. Chem. Lett. 1999, 9, 91-96.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 91-96
-
-
Imbach, P.1
Capraro, H.-G.2
Furet, P.3
Mett, H.4
Meyer, T.5
Zimmermann, J.6
-
22
-
-
0032563315
-
Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors
-
Gray, N. S.; Wodicka, L.; Thunnissen, A.-M. W. H.; Norman, T. C.; Kwon, S.; Espinoza, F. H.; Morgan, D. O.; Barnes, G.; LeClerc, S.; Meijer, L.; Kim, S.-H.; Lockhart, D. J.; Schultz, P. G. Exploiting Chemical Libraries, Structure, and Genomics in the Search for Kinase Inhibitors. Science 1998, 281, 533-538.
-
(1998)
Science
, vol.281
, pp. 533-538
-
-
Gray, N.S.1
Wodicka, L.2
Thunnissen, A.-M.W.H.3
Norman, T.C.4
Kwon, S.5
Espinoza, F.H.6
Morgan, D.O.7
Barnes, G.8
LeClerc, S.9
Meijer, L.10
Kim, S.-H.11
Lockhart, D.J.12
Schultz, P.G.13
-
23
-
-
0030869845
-
Synthesis and activity of 2,6,9-trisubstituted purines
-
Schow, S. R.; Mackman, R. L.; Blum, C. L.; Brooks, E.; Horsma, A. G.; Joly, A.; Kerwar, S. S.; Lee, G.; Shiffman, D.; Nelson, M. G.; Wang, X.; Wick, M. M.; Zhang, X.; Lum, R. T. Synthesis and Activity of 2,6,9-Trisubstituted Purines. Bioorg. Med. Chem. Lett. 1997, 7, 2697-2702.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2697-2702
-
-
Schow, S.R.1
Mackman, R.L.2
Blum, C.L.3
Brooks, E.4
Horsma, A.G.5
Joly, A.6
Kerwar, S.S.7
Lee, G.8
Shiffman, D.9
Nelson, M.G.10
Wang, X.11
Wick, M.M.12
Zhang, X.13
Lum, R.T.14
-
24
-
-
15444355744
-
CVT-313, a specific and potent inhibitor of CDK2 that prevents neointimal proliferation
-
Brooks, E. E.; Gray, N. S.; Joly, A.; Kerwar, S. S.; Lum, R.; Mackman, R. L.; Norman, T. C.; Rosete, J.; Rowe, M.; Schow, S. R.; Schultz, P. G.; Wang, X.; Wick, M. M.; Shiffman, D. CVT-313, A Specific and Potent Inhibitor of CDK2 That Prevents Neointimal Proliferation. J. Biol. Chem. 1997, 272, 29207-29211.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 29207-29211
-
-
Brooks, E.E.1
Gray, N.S.2
Joly, A.3
Kerwar, S.S.4
Lum, R.5
Mackman, R.L.6
Norman, T.C.7
Rosete, J.8
Rowe, M.9
Schow, S.R.10
Schultz, P.G.11
Wang, X.12
Wick, M.M.13
Shiffman, D.14
-
25
-
-
0031055563
-
Cytokinin-derived cyclin-dependent kinase inhibitors: Synthesis and cdc2 inhibitory activity of olomoucine and related compounds
-
Havlíček, L.; Hanuš, J.; Veselý, J.; Leclerc, S.; Meijer, L.; Shaw, G.; Strnad, M. Cytokinin-Derived Cyclin-Dependent Kinase Inhibitors: Synthesis and cdc2 Inhibitory Activity of Olomoucine and Related Compounds. J. Med. Chem. 1997, 40, 408-412.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 408-412
-
-
Havlíček, L.1
Hanuš, J.2
Veselý, J.3
Leclerc, S.4
Meijer, L.5
Shaw, G.6
Strnad, M.7
-
26
-
-
0031037714
-
Biochemical and cellular effects of roscovitine, a potent and selective inhihibitor of the cyclin-dependent kinases cdc2, cdk2, and cdk5
-
Meijer, L.; Borgne, A.; Mulner, O.; Chong, J. P. J.; Blow, J. J.; Inagaki, N.; Inagaki, M.; Delcros, J.-G.; Moulinoux, J.-P. Biochemical and cellular effects of roscovitine, a potent and selective inhihibitor of the cyclin-dependent kinases cdc2, cdk2, and cdk5. Eur. J. Biochem. 1997, 243, 527-536.
-
(1997)
Eur. J. Biochem.
, vol.243
, pp. 527-536
-
-
Meijer, L.1
Borgne, A.2
Mulner, O.3
Chong, J.P.J.4
Blow, J.J.5
Inagaki, N.6
Inagaki, M.7
Delcros, J.-G.8
Moulinoux, J.-P.9
-
27
-
-
0028093182
-
Inhibition of cyclin-dependent kinases by purine analogues
-
Veselý, J.; Havlíček, L.; Strnad, M.; Blow, J. J.; Donella-Deana, A.; Pinna, L.; Letham, D. S.; Kato, J.-Y.; Detivaud, L.; LeClerc, S.; Meijer, L. Inhibition of cyclin-dependent kinases by purine analogues. Eur. J. Biochem. 1994, 224, 771-786.
-
(1994)
Eur. J. Biochem.
, vol.224
, pp. 771-786
-
-
Veselý, J.1
Havlíček, L.2
Strnad, M.3
Blow, J.J.4
Donella-Deana, A.5
Pinna, L.6
Letham, D.S.7
Kato, J.-Y.8
Detivaud, L.9
LeClerc, S.10
Meijer, L.11
-
28
-
-
0037058678
-
In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R-Roscovitine)
-
McClue, S. J.; Blake, D.; Clarke, R.; Cowan, A.; Cummings, L.; Fischer, P. M.; MacKenzie, M.; Melville, J.; Stewart, J. K.; Wang, S.; Zhelev, N.; Zheleva, D.; Lane, D. P. In Vitro and IN Vivo Antitumor Properties of the Cyclin Dependent Kinase Inhibitor CYC202 (R-Roscovitine). Int. J. Cancer 2002, 102, 463-468.
-
(2002)
Int. J. Cancer.
, vol.102
, pp. 463-468
-
-
McClue, S.J.1
Blake, D.2
Clarke, R.3
Cowan, A.4
Cummings, L.5
Fischer, P.M.6
MacKenzie, M.7
Melville, J.8
Stewart, J.K.9
Wang, S.10
Zhelev, N.11
Zheleva, D.12
Lane, D.P.13
-
29
-
-
0033152122
-
Discovery and initial characterization of the paullones, a novel class of small-molecule inhibitors of cyclin-dependent kinases
-
Zaharevitz, D. W.; Gussio, R.; Leost, M.; Senderowicz, A. M.; Lahusen, T.; Kunick, C.; Meijer, L.; Sausville, E. A. Discovery and Initial Characterization of the Paullones, a Novel Class of Small-Molecule Inhibitors of Cyclin-dependent Kinases. Cancer Res. 1999, 59, 2566-2569.
-
(1999)
Cancer Res.
, vol.59
, pp. 2566-2569
-
-
Zaharevitz, D.W.1
Gussio, R.2
Leost, M.3
Senderowicz, A.M.4
Lahusen, T.5
Kunick, C.6
Meijer, L.7
Sausville, E.A.8
-
30
-
-
0034089542
-
Structure-based design modifications of the paullone molecular scaffold for cyclin-dependent kinase inhibition
-
Gussio, R.; Zaharevitz, D. W.; McGrath, C. F.; Pattabiraman, N.; Kellogg, G. E.; Schultz, C.; Link, A.; Kunick, C.; Leost, M.; Meijer, L.; Sausville, E. A. Structure-based design modifications of the paullone molecular scaffold for cyclin-dependent kinase inhibition. Anti-Cancer Drug Des. 2000, 15, 53-66.
-
(2000)
Anti-Cancer Drug Des.
, vol.15
, pp. 53-66
-
-
Gussio, R.1
Zaharevitz, D.W.2
McGrath, C.F.3
Pattabiraman, N.4
Kellogg, G.E.5
Schultz, C.6
Link, A.7
Kunick, C.8
Leost, M.9
Meijer, L.10
Sausville, E.A.11
-
31
-
-
0034689596
-
2-Substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity
-
Kunick, C.; Schultz, C.; Lemcke, T.; Zaharevitz, D. W.; Gussio, R.; Jalluri, R. K.; Sausville, E. A.; Leost, M.; Meijer, L. 2-Substituted Paullones: CDK1/Cyclin B-Inhibiting Property and In Vitro Antiproliferative Activity. Bioorg. Med. Chem. Lett. 2000, 10, 567-569.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 567-569
-
-
Kunick, C.1
Schultz, C.2
Lemcke, T.3
Zaharevitz, D.W.4
Gussio, R.5
Jalluri, R.K.6
Sausville, E.A.7
Leost, M.8
Meijer, L.9
-
32
-
-
0033614949
-
Paullones, a series of cyclin-dependent kinase inhibitors: Synthesis, evaluation of CDK1/cyclin B inhibition, and in vitro antitumor activity
-
Schultz, C.; Link, A.; Loest, M.; Zaharevitz, D. W.; Gussio, R.; Sausville, E. A.; Meijer, L.; Kunick, C. Paullones, A Series of Cyclin-Dependent Kinase Inhibitors: Synthesis, Evaluation of CDK1/Cyclin B Inhibition, and in Vitro Antitumor Activity. J. Med. Chem. 1999, 42, 2909-2919.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 2909-2919
-
-
Schultz, C.1
Link, A.2
Loest, M.3
Zaharevitz, D.W.4
Gussio, R.5
Sausville, E.A.6
Meijer, L.7
Kunick, C.8
-
33
-
-
0034689596
-
2-Substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity
-
Kunick, C.; Schultz, C.; Lemcke, T.; Zaharevitz, D. W.; Gussio, R.; Jalluri, R. K.; Sausville, E. A.; Loest, M.; Meijer, L. 2-Substituted Paullones: CDK1/Cyclin B-Inhibiting Property and In Vitro Antiproliferative Activity. Bioorg. Med. Chem. Lett. 2000, 10, 567-569.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 567-569
-
-
Kunick, C.1
Schultz, C.2
Lemcke, T.3
Zaharevitz, D.W.4
Gussio, R.5
Jalluri, R.K.6
Sausville, E.A.7
Loest, M.8
Meijer, L.9
-
34
-
-
12444339387
-
Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6- aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2
-
Sayle, K. L.; Bentley, J.; Boyle, F. T.; Calvert, A. H.; Cheng, Y.; Curtin, N. J.; Endicott, J. A.; Golding, B. T.; Hardcastle, I. R.; Jewsbury, P.; Mesguiche, V.; Newell, D. R.; Noble, M. E. M., Parsons, R. J., Pratt, D. J.; Wang, L. Z.; Griffin, R. J. Structure-Based Design of 2-Arylamino-4- cyclohexylmethyl-5-nitroso-6-aminopyrimidine Inhibitors of Cyclin-Dependent Kinases 1 and 2. Bioorg. Med. Chem. Lett. 2003, 13, 3079-3082.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3079-3082
-
-
Sayle, K.L.1
Bentley, J.2
Boyle, F.T.3
Calvert, A.H.4
Cheng, Y.5
Curtin, N.J.6
Endicott, J.A.7
Golding, B.T.8
Hardcastle, I.R.9
Jewsbury, P.10
Mesguiche, V.11
Newell, D.R.12
Noble, M.E.M.13
Parsons, R.J.14
Pratt, D.J.15
Wang, L.Z.16
Griffin, R.J.17
-
35
-
-
12444257368
-
Imidazo[1,2-α]pyridines: A potent and selective class of cyclin-dependent kinase inhibitors indentified through structure-based hybridisation
-
Anderson, M.; Beattie, J. F.; Breault, G. A.; Breed, J.; Byth, K. F.; Culshaw, J. D.; Ellston, R. P. A.; Green, S.; Minshull, C. A.; Norman, R. A.; Pauptit, R. A.; Stanway, J.; Thomas, A. P.; Jewsbury, P. J. Imidazo[1,2-α] pyridines: A Potent and Selective Class of Cyclin-Dependent Kinase Inhibitors Indentified Through Structure-Based Hybridisation. Bioorg. Med. Chem. Lett. 2003, 13, 3021-3026.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3021-3026
-
-
Anderson, M.1
Beattie, J.F.2
Breault, G.A.3
Breed, J.4
Byth, K.F.5
Culshaw, J.D.6
Ellston, R.P.A.7
Green, S.8
Minshull, C.A.9
Norman, R.A.10
Pauptit, R.A.11
Stanway, J.12
Thomas, A.P.13
Jewsbury, P.J.14
-
36
-
-
0041519342
-
Anilinopyrazole as selective CDK2 inhibitors: Design, synthesis, biological evaluation, and X-ray crystallographic analysis
-
Tang, J.; Shewchuk, L. M.; Sato, H.; Hasegawa, M.; Washio, Y.; Nishigaki, N. Anilinopyrazole as Selective CDK2 Inhibitors: Design, Synthesis, Biological Evaluation, and X-ray Crystallographic Analysis. Bioorg. Med. Chem. Lett. 2003, 13, 2985-2988.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2985-2988
-
-
Tang, J.1
Shewchuk, L.M.2
Sato, H.3
Hasegawa, M.4
Washio, Y.5
Nishigaki, N.6
-
37
-
-
12444260278
-
LH-pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinases: Highly potent 2,6-difluorophenacyl analogues
-
Misra, R. N.; Xiao, H.; Rawlins, D. B.; Shan, W.; Kellar, K. A.; Mulheron, J. G.; Sack, J. S.; Tokarski, J. S.; Kimball, S. D.; Webster, K. R. LH-Pyrazolo[3,4-b]pyridine Inhibitors of Cyclin-Dependent Kinases: Highly Potent 2,6-Difluorophenacyl Analogues. Bioorg. Med. Chem. Lett. 2003, 13, 2405-2408.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2405-2408
-
-
Misra, R.N.1
Xiao, H.2
Rawlins, D.B.3
Shan, W.4
Kellar, K.A.5
Mulheron, J.G.6
Sack, J.S.7
Tokarski, J.S.8
Kimball, S.D.9
Webster, K.R.10
-
38
-
-
0037463754
-
1H-Pyrazolo[3,4-o]pyridine inhibitors of cyclin-dependent kinases
-
Misra, R. N.; Rawlins, D. B.; Xiao, H.; Shan, W.; Bursuker, I.; Kellar, K. A.; Mulheron, J. G.; Sack, J. S.; Tokarski, J. S.; Kimball, S. D.; Webster, K. R. 1H-Pyrazolo[3,4-o]pyridine Inhibitors of Cyclin-Dependent Kinases. Bioorg. Med. Chem. Lett. 2003, 13, 1133-1136.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1133-1136
-
-
Misra, R.N.1
Rawlins, D.B.2
Xiao, H.3
Shan, W.4
Bursuker, I.5
Kellar, K.A.6
Mulheron, J.G.7
Sack, J.S.8
Tokarski, J.S.9
Kimball, S.D.10
Webster, K.R.11
-
39
-
-
18744404784
-
4-Alkoxy-2,6-diaminopyrimidine derivatives: Inhibitors of cyclin dependent kinases 1 and 2
-
Mesguiche, V.; Parsons, R. J.; Arris, C. E.; Bentley, J.; Boyle, F. T.; Curtin, N. J.; Davies, T. G.; Endicott, J. A.; Gibson, A. E.; Golding, B. T.; Griffin, R. J.; Jewsbury, P.; Johnson, L. N.; Newell, D. R.; Noble, M. E. M.; Wang, L. Z.; Hardcastle, I. R. 4-Alkoxy-2,6-diaminopyrimidine Derivatives: Inhibitors of Cyclin Dependent Kinases 1 and 2. Bioorg. Med. Chem. Lett. 2003, 13, 217-222.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 217-222
-
-
Mesguiche, V.1
Parsons, R.J.2
Arris, C.E.3
Bentley, J.4
Boyle, F.T.5
Curtin, N.J.6
Davies, T.G.7
Endicott, J.A.8
Gibson, A.E.9
Golding, B.T.10
Griffin, R.J.11
Jewsbury, P.12
Johnson, L.N.13
Newell, D.R.14
Noble, M.E.M.15
Wang, L.Z.16
Hardcastle, I.R.17
-
40
-
-
0037041190
-
β-carbolines as specific inhibitors of cyclin-dependent kinases
-
Song, Y.; Wang, J.; Teng, S. F.; Kesuma, D.; Deng, Y.; Duan, J.; Wang, J. H.; Qi, R. Z.; Sim, M. M. β-Carbolines as Specific Inhibitors of Cyclin-Dependent Kinases. Bioorg. Med. Chem. Lett. 2002, 12, 1129-1132.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1129-1132
-
-
Song, Y.1
Wang, J.2
Teng, S.F.3
Kesuma, D.4
Deng, Y.5
Duan, J.6
Wang, J.H.7
Qi, R.Z.8
Sim, M.M.9
-
41
-
-
0037194619
-
Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: Synthesis, X-ray crystallographic analysis, and biological activities
-
Kim, K. S.; Kimball, S. D.; Misra, R. N.; Rawlins, D. B.; Hunt, J. T.; Xiao, H.-Y.; Lu, S.; Qian, L.; Han, W.-C.; Shan, W.; Mitt, T.; Cai, Z.-W.; Poss, M. A.; Zhu, H.; Sack, J. S.; Tokarski, J. S.; Chang, C. Y.; Pavletich, N.; Kamath, A.; Humphreys, W. G.; Marathe, P.; Bursuker, I.; Kellar, K. A.; Roongta, U.; Batorsky, R.; Mulheron, J. G.; Bol, D.; Fairchild, C. R.; Lee, F. Y.; Webster, K. R. Discovery of Aminothiazole Inhibitors of Cyclin-Dependent Kinase 2: Synthesis, X-ray Crystallographic Analysis, and Biological Activities. J. Med. Chem. 2002, 45, 3905-3927.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3905-3927
-
-
Kim, K.S.1
Kimball, S.D.2
Misra, R.N.3
Rawlins, D.B.4
Hunt, J.T.5
Xiao, H.-Y.6
Lu, S.7
Qian, L.8
Han, W.-C.9
Shan, W.10
Mitt, T.11
Cai, Z.-W.12
Poss, M.A.13
Zhu, H.14
Sack, J.S.15
Tokarski, J.S.16
Chang, C.Y.17
Pavletich, N.18
Kamath, A.19
Humphreys, W.G.20
Marathe, P.21
Bursuker, I.22
Kellar, K.A.23
Roongta, U.24
Batorsky, R.25
Mulheron, J.G.26
Bol, D.27
Fairchild, C.R.28
Lee, F.Y.29
Webster, K.R.30
more..
-
42
-
-
0036242381
-
Pyrazolo[3,4-b]quinoxalines. A new class of cyclin-dependent kinases inhibitors
-
Ortega, M. A.; Montoya, M. E.; Zarranz, B.; Jaso, A.; Aldana, I.; Leclerc, S.; Meijer, L.; Monge, A. Pyrazolo[3,4-b]quinoxalines. A New Class of Cyclin-Dependent Kinases Inhibitors. Bioorg. Med. Chem. Lett. 2002, 10, 2177-2184.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2177-2184
-
-
Ortega, M.A.1
Montoya, M.E.2
Zarranz, B.3
Jaso, A.4
Aldana, I.5
Leclerc, S.6
Meijer, L.7
Monge, A.8
-
43
-
-
0037147768
-
Structure-based design and protein X-ray analysis of a protein kinase inhibitor
-
Furet, P.; Meyer, T.; Strauss, A.; Raccuglia, S.; Rondeau, J.-M. Structure-Based Design and Protein X-ray Analysis of a Protein Kinase Inhibitor. Bioorg. Med. Chem. Lett. 2002, 12, 221-224.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 221-224
-
-
Furet, P.1
Meyer, T.2
Strauss, A.3
Raccuglia, S.4
Rondeau, J.-M.5
-
44
-
-
0035808599
-
Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors
-
Davis, S. T.; Benson, B. G.; Bramson, H. N.; Chapman, D. E.; Dickerson, S. H.; Dold, K. M.; Eberwein, D. J.; Edelstein, M.; Frye, S. V.; Gampe, R. T., Jr.; Griffin, R. J.; Harris, P. A.; Hassell, A. M.; Holmes, W. D.; Hunter, R. N.; Knick, V. B.; Lackey, K.; Lovejoy, B.; Luzzio, M. J.; Murray, D.; Parker, P.; Rocque, W. J.; Shewchuk, L.; Veal, J. M.; Walker, D. H.; Kuyper, L. F. Prevention of Chemotherapy-Induced Alopecia in Rats by CDK Inhibitors. Science 2001, 291, 134-137.
-
(2001)
Science
, vol.291
, pp. 134-137
-
-
Davis, S.T.1
Benson, B.G.2
Bramson, H.N.3
Chapman, D.E.4
Dickerson, S.H.5
Dold, K.M.6
Eberwein, D.J.7
Edelstein, M.8
Frye, S.V.9
Gampe Jr., R.T.10
Griffin, R.J.11
Harris, P.A.12
Hassell, A.M.13
Holmes, W.D.14
Hunter, R.N.15
Knick, V.B.16
Lackey, K.17
Lovejoy, B.18
Luzzio, M.J.19
Murray, D.20
Parker, P.21
Rocque, W.J.22
Shewchuk, L.23
Veal, J.M.24
Walker, D.H.25
Kuyper, L.F.26
more..
-
45
-
-
0035821336
-
Quinazolines as cyclin dependent kinase inhibitors
-
Sielecki, T. M.; Johnson, T. L.; Liu, J.; Muckelbauer, J. K.; Grafstrom, R. H.; Cox, S.; Boylan, J.; Burton, C. R.; Chen, H.; Smallwood, A.; Chang, C.-H.; Boisclair, M.; Benfield, P. A.; Trainor, G. L.; Seitz, S. P. Quinazolines as Cyclin Dependent Kinase Inhibitors. Bioorg. Med. Chem. Lett. 2001, 11, 1157-1160.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1157-1160
-
-
Sielecki, T.M.1
Johnson, T.L.2
Liu, J.3
Muckelbauer, J.K.4
Grafstrom, R.H.5
Cox, S.6
Boylan, J.7
Burton, C.R.8
Chen, H.9
Smallwood, A.10
Chang, C.-H.11
Boisclair, M.12
Benfield, P.A.13
Trainor, G.L.14
Seitz, S.P.15
-
46
-
-
0035015532
-
Identification of cyclin-dependent kinase 1 inhibitors of a new chemical type by structure-based design and database searching
-
Furet, P.; Meyer, T.; Mittl, P.; Fretz, H. Identification of cyclin-dependent kinase 1 inhibitors of a new chemical type by structure-based design and database searching. J. Comput.-Aided Mol. Des. 2001, 15, 489-495.
-
(2001)
J. Comput.-Aided Mol. Des.
, vol.15
, pp. 489-495
-
-
Furet, P.1
Meyer, T.2
Mittl, P.3
Fretz, H.4
-
47
-
-
0032080613
-
Design of new inhibitors for CDC2 kinase based on a multiple pseudosubstrate structure
-
Sasaki, S.; Hashimoto, T.; Obana, N.; Yasuda, H.; Uehara, Y.; Maeda, M. Design of New Inhibitors for CDC2 Kinase Based on a Multiple Pseudosubstrate Structure. Bioorg. Med. Chem. Lett. 1988, 8, 1019-1022.
-
(1988)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1019-1022
-
-
Sasaki, S.1
Hashimoto, T.2
Obana, N.3
Yasuda, H.4
Uehara, Y.5
Maeda, M.6
-
48
-
-
10744229843
-
Characterization of a novel cyclin-dependent kinase 1 inhibitor, BMI-1026
-
Seong, Y.-S.; Min, C.; Li, L.; Yang, J. Y.; Kim, S.-Y.; C. X.; Kim, K.; Yuspa, S. H.; Chung, H.-H.; Lee, K. S. Characterization of a Novel Cyclin-Dependent Kinase 1 Inhibitor, BMI-1026. Cancer Res. 2003, 63, 7384-7391.
-
(2003)
Cancer Res.
, vol.63
, pp. 7384-7391
-
-
Seong, Y.-S.1
Min, C.2
Li, L.3
Yang, J.Y.4
Kim, S.-Y.5
Kim, K.6
Yuspa, S.H.7
Chung, H.-H.8
Lee, K.S.9
-
49
-
-
0034657527
-
Structure-activity relationship studies of flavopiridol analogues
-
Murthi, K. K.; Dubay, M.; McClure, C.; Brizuela, L.; Boisclair, M. D.; Worland, P. J.; Mansuri, M. M.; Pal, K. Structure-Activity Relationship Studies of Flavopiridol Analogues. Bioorg. Med. Chem. Lett. 2000, 10, 1037-1041.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1037-1041
-
-
Murthi, K.K.1
Dubay, M.2
McClure, C.3
Brizuela, L.4
Boisclair, M.D.5
Worland, P.J.6
Mansuri, M.M.7
Pal, K.8
-
50
-
-
0038394493
-
Novel pyrrolyllactone and pyrrolyllactam indolinones as potent cyclin-dependent kinase 2 inhibitors
-
Li, X.; Huang, P.; Cui, J. J.; Zhang, J.; Tang, C. Novel Pyrrolyllactone and Pyrrolyllactam Indolinones as Potent Cyclin-Dependent Kinase 2 Inhibitors. Bioorg. Med. Chem. Lett. 2003, 13, 1939-1942.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1939-1942
-
-
Li, X.1
Huang, P.2
Cui, J.J.3
Zhang, J.4
Tang, C.5
-
51
-
-
10744231650
-
3,5,6-Trisubstituted naphthostyrils as CDK2 inhibitors
-
Liu, J.-J.; Dermatakis, A.; Lukacs, C.; Konzelmann, F.; Chen, Y.; Kammlott, U.; Depinto, W.; Yang, H.; Yin, X.; Chen, Y.; Schutt, A.; Simcox, M. E.; Luk, K.-C. 3,5,6-Trisubstituted Naphthostyrils as CDK2 Inhibitors. Bioorg. Med. Chem. Lett. 2003, 13, 2465-2468.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2465-2468
-
-
Liu, J.-J.1
Dermatakis, A.2
Lukacs, C.3
Konzelmann, F.4
Chen, Y.5
Kammlott, U.6
Depinto, W.7
Yang, H.8
Yin, X.9
Chen, Y.10
Schutt, A.11
Simcox, M.E.12
Luk, K.-C.13
-
52
-
-
0035818942
-
Oxindole-based inhibitors of cyclin-dependent kinase 2 (CDK2): Design, synthesis, enzymatic activities, and X-ray crystallographic analysis
-
Bramson, H. N.; Corona, J.; Davis, S. T.; Dickerson, S. H.; Edelstein, M.; Frye, S. V.; Gampe, R. T., Jr.; Harris, P. A.; Hassell, A.; Holmes, W. D.; Hunter, R. N.; Lackey, K. E.; Lovejoy, B.; Luzzio, M. J.; Montana, V.; Rocque, W. J.; Rusnak, D.; Shewchuk, L.; Veal, J. M.; Walker, D. H.; Kuyper, L. F. Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design, Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis. J. Med. Chem. 2001, 44, 4339-4358.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4339-4358
-
-
Bramson, H.N.1
Corona, J.2
Davis, S.T.3
Dickerson, S.H.4
Edelstein, M.5
Frye, S.V.6
Gampe Jr., R.T.7
Harris, P.A.8
Hassell, A.9
Holmes, W.D.10
Hunter, R.N.11
Lackey, K.E.12
Lovejoy, B.13
Luzzio, M.J.14
Montana, V.15
Rocque, W.J.16
Rusnak, D.17
Shewchuk, L.18
Veal, J.M.19
Walker, D.H.20
Kuyper, L.F.21
more..
-
53
-
-
0037153215
-
Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. 3. Structure activity relationships at C3
-
Yue, E. W.; Higley, C. A.; DiMeo, S. V.; Carini, D. J.; Nugiel, D. A.; Benware, C.; Benfield, P. A.; Burton, C. R.; Cox, S.; Grafstrom, R. H.; Sharp, D. M.; Sisk, L. M.; Boylan, J. F.; Muckelbauer, J. K.; Smallwood, A. M.; Chen, H.; Chang, C.-H.; Seitz, S. P.; Trainor, G. L. Synthesis and Evaluation of Indenopyrazoles as Cyclin-Dependent Kinase Inhibitors. 3.Structure Activity Relationships at C3. J. Med. Chem. 2002, 45, 5233-5248.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5233-5248
-
-
Yue, E.W.1
Higley, C.A.2
DiMeo, S.V.3
Carini, D.J.4
Nugiel, D.A.5
Benware, C.6
Benfield, P.A.7
Burton, C.R.8
Cox, S.9
Grafstrom, R.H.10
Sharp, D.M.11
Sisk, L.M.12
Boylan, J.F.13
Muckelbauer, J.K.14
Smallwood, A.M.15
Chen, H.16
Chang, C.-H.17
Seitz, S.P.18
Trainor, G.L.19
-
54
-
-
0037153230
-
Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. 2. Probing the indeno ring substituent pattern
-
Nugiel, D. A.; Vidwans, A.; Etzkorn, A.-M.; Rossi, K. A.; Benfield, P. A.; Burton, C. R.; Cox, S.; Doleniak, D.; Seitz, S. P. Synthesis and Evaluation of Indenopyrazoles as Cyclin-Dependent Kinase Inhibitors. 2. Probing the Indeno Ring Substituent Pattern. J. Med. Chem. 2002, 45, 5224-5232.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5224-5232
-
-
Nugiel, D.A.1
Vidwans, A.2
Etzkorn, A.-M.3
Rossi, K.A.4
Benfield, P.A.5
Burton, C.R.6
Cox, S.7
Doleniak, D.8
Seitz, S.P.9
-
55
-
-
0035953327
-
Indenopyrazoles as novel Cyclin Dependent Kinase (CDK) inhibitors
-
Nugiel, D. A.; Etzkorn, A.-M.; Vidwans, A.; Benfield, P. A.; Boisclair, M.; Burton, C. R.; Cox, S.; Czerniak, P. M.; Doleniak, D.; Seitz, S. P. Indenopyrazoles as Novel Cyclin Dependent Kinase (CDK) Inhibitors. J. Med. Chem. 2001, 44, 1334-1336.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1334-1336
-
-
Nugiel, D.A.1
Etzkorn, A.-M.2
Vidwans, A.3
Benfield, P.A.4
Boisclair, M.5
Burton, C.R.6
Cox, S.7
Czerniak, P.M.8
Doleniak, D.9
Seitz, S.P.10
-
56
-
-
0035881591
-
A novel cdk2-selective inhibitor, SU9516, induces apoptosis in colon carcinoma cells
-
Lane, M. E.; Yu, B.; Rice, A.; Lipson, K. E.; Liang, C.; Sun, L.; Tang, C.; McMahon, G.; Pestell, R. G.; Wadler, S. A Novel cdk2-selective Inhibitor, SU9516, Induces Apoptosis in Colon Carcinoma Cells. Cancer Res. 2001, 61, 6170-6177.
-
(2001)
Cancer Res.
, vol.61
, pp. 6170-6177
-
-
Lane, M.E.1
Yu, B.2
Rice, A.3
Lipson, K.E.4
Liang, C.5
Sun, L.6
Tang, C.7
McMahon, G.8
Pestell, R.G.9
Wadler, S.10
-
57
-
-
0034434429
-
Imidazo[2,1-b]thiazolylmethylene- and indolylmethylene-2-indolinones: A new class of cyclin-dependent kinase inhibitors. Design, synthesis, and CDK/cyclin B inhibition
-
Andreani, A.; Cavalli, A.; Granaiola, M.; Leoni, A.; Locatelli, A.; Morigi, R.; Rambaldi, M.; Recanatini, M.; Gamier, M.; Meijer, L. Imidazo[2,1-b]thiazolylmethylene- and indolylmethylene-2-indolinones: a new class of cyclin-dependent kinase inhibitors. Design, synthesis, and CDK/cyclin B inhibition. Anti-Cancer Drug Des. 2000, 15, 447-452.
-
(2000)
Anti-Cancer Drug Des.
, vol.15
, pp. 447-452
-
-
Andreani, A.1
Cavalli, A.2
Granaiola, M.3
Leoni, A.4
Locatelli, A.5
Morigi, R.6
Rambaldi, M.7
Recanatini, M.8
Gamier, M.9
Meijer, L.10
-
58
-
-
0035924235
-
Structure-based generation of a new class of potent Cdk4 inhibitors: New de Novo design strategy and library design
-
Honma, T.; Hayaski, K.; Aoyama, T.; Hashimoto, N.; Machida, T.; Fukasawa, K.; Iwama, T.; Ikeura, C.; Ikuta, M.; Suzuki-Takahashi, L; Iwasawa, Y.; Hayama, T.; Nishimura, S.; Morishima, H. Structure-Based Generation of a New Class of Potent Cdk4 Inhibitors: New de Novo Design Strategy and Library Design. J. Med. Chem. 2001, 44, 4615-4627.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4615-4627
-
-
Honma, T.1
Hayaski, K.2
Aoyama, T.3
Hashimoto, N.4
Machida, T.5
Fukasawa, K.6
Iwama, T.7
Ikeura, C.8
Ikuta, M.9
Suzuki-Takahashi, L.10
Iwasawa, Y.11
Hayama, T.12
Nishimura, S.13
Morishima, H.14
-
59
-
-
0035924240
-
A novel approach for the development of selective Cdk4 inhibitors: Library design based on locations of Cdk4 specific amino acid residues
-
Honma, T.; Yoshizumi, T.; Hashimoto, N.; Hayashi, K.; Kawanishi, N.; Fukasawa, K.; Takaki, T.; Ikeura, C.; Ikuta, M.; Suzuki-Takahashi, I.; Hayama, T.; Nishimura, S.; Moroshima, H. A Novel Approach for the Development of Selective Cdk4 Inhibitors: Library Design Based on Locations of Cdk4 Specific Amino Acid residues. J. Med. Chem. 2001, 44, 4628-4640.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4628-4640
-
-
Honma, T.1
Yoshizumi, T.2
Hashimoto, N.3
Hayashi, K.4
Kawanishi, N.5
Fukasawa, K.6
Takaki, T.7
Ikeura, C.8
Ikuta, M.9
Suzuki-Takahashi, I.10
Hayama, T.11
Nishimura, S.12
Moroshima, H.13
-
60
-
-
0035925574
-
Selective in vivo and in vitro effects of a small molecule inhibitor of cyclin-dependent kinase 4
-
Soni, R.; O'Reilly, T.; Furet, P.; Muller, L.; Stephan, C.; Zumstein-Mecker, S.; Fretz, H.; Fabbro, D.; Chaudhuri, B. Selective In Vivo and In Vitro Effects of a Small Molecule Inhibitor of Cyclin-Dependent Kinase 4. J. Natl. Cancer Inst. 2001, 93, 436-446.
-
(2001)
J. Natl. Cancer Inst.
, vol.93
, pp. 436-446
-
-
Soni, R.1
O'Reilly, T.2
Furet, P.3
Muller, L.4
Stephan, C.5
Zumstein-Mecker, S.6
Fretz, H.7
Fabbro, D.8
Chaudhuri, B.9
-
61
-
-
12444262227
-
Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 1: Identification and optimisation of substituted 4,6-bis anilino pyrimidines
-
Beattie, J. F.; Breault, G. A.; Ellston, R. P. A.; Green, S.; Jewsbury, P. J.; Midgley, C. J.; Naven, R. T.; Minshull, C. A.; Pauptit, R. A.; Tucker, J. A.; Pease, J. E. Cyclin-Dependent Kinase 4 Inhibitors as a Treatment for Cancer. Part 1: Identification and Optimisation of Substituted 4,6-Bis Anilino Pyrimidines. Bioorg. Med. Chem. Lett. 2003, 13, 2955-2960.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2955-2960
-
-
Beattie, J.F.1
Breault, G.A.2
Ellston, R.P.A.3
Green, S.4
Jewsbury, P.J.5
Midgley, C.J.6
Naven, R.T.7
Minshull, C.A.8
Pauptit, R.A.9
Tucker, J.A.10
Pease, J.E.11
-
62
-
-
12444273643
-
Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 2: Identification as optimisation of substituted 2,4-bis anilino pyrimidines
-
Breault, G. A.; Ellston, R. P. A.; Green, S.; James, S. R.; Jewsbury, P. J.; Midgley, C. J.; Pauptit, R. A.; C. A.; Minshull, Tucker, J. A.; Pease, J. E. Cyclin-Dependent Kinase 4 Inhibitors as a Treatment for Cancer. Part 2: Identification as Optimisation of Substituted 2,4-Bis Anilino Pyrimidines. Bioorg. Med. Chem. Lett. 2003, 13, 2961-2966.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2961-2966
-
-
Breault, G.A.1
Ellston, R.P.A.2
Green, S.3
James, S.R.4
Jewsbury, P.J.5
Midgley, C.J.6
Pauptit, R.A.7
Minshull, C.A.8
Tucker, J.A.9
Pease, J.E.10
-
63
-
-
12444304196
-
Aryl-[α]pyrrolo[3,4,-c]carbazoles as selective cyclin D1-CDK4 inhibitors
-
Sanchez-Martinez, C.; Shih, C.; Faul, M. M.; Zhu, G.; Paal, M.; Somoza, C.; Li, T.; Kumrich, C. A.; Winneroski, L. L.; Xun, Z.; Brooks, H. B.; Patel, B. K. R.; Schultz, R. M.; DeHahn, T. B.; Spencer, C. D.; Watkins, S. A.; Considine, E.; Dempsey, J. A.; Ogg, C. A.; Campbell, R. M.; Anderson, B. A.; Wagner, J. Aryl-[α]pyrrolo[3,4,-c]carbazoles as Selective Cyclin D1-CDK4 Inhibitors. Bioorg. Med. Chem. Lett. 2003, 13, 3835-3839.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3835-3839
-
-
Sanchez-Martinez, C.1
Shih, C.2
Faul, M.M.3
Zhu, G.4
Paal, M.5
Somoza, C.6
Li, T.7
Kumrich, C.A.8
Winneroski, L.L.9
Xun, Z.10
Brooks, H.B.11
Patel, B.K.R.12
Schultz, R.M.13
DeHahn, T.B.14
Spencer, C.D.15
Watkins, S.A.16
Considine, E.17
Dempsey, J.A.18
Ogg, C.A.19
Campbell, R.M.20
Anderson, B.A.21
Wagner, J.22
more..
-
64
-
-
12444282655
-
Studies on cyclin-dependent kinase inhibitors: Indolo-[2,3-α] pyrrolo[3,4-c]carbazoles versus bis-indolylmaleimides
-
Sanchez-Martinez, C.; Shih, C.; Zhu, G.; Li, T.; Brooks, H. B.; Patel, B. K. R.; Schultz, R. M.; DeHahn, T. B.; Spencer, C. D.; Watkins, S. A.; Ogg, C. A.; Considine, E.; Dempsey, J. A.; Zhang, F. Studies on Cyclin-Dependent Kinase Inhibitors: Indolo-[2,3-α]pyrrolo[3,4-c]carbazoles versus Bis-indolylmaleimides. Bioorg. Med. Chem. Lett. 2003, 13, 3841-3846.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3841-3846
-
-
Sanchez-Martinez, C.1
Shih, C.2
Zhu, G.3
Li, T.4
Brooks, H.B.5
Patel, B.K.R.6
Schultz, R.M.7
DeHahn, T.B.8
Spencer, C.D.9
Watkins, S.A.10
Ogg, C.A.11
Considine, E.12
Dempsey, J.A.13
Zhang, F.14
-
65
-
-
12444308937
-
Novel, potent and selective cyclin D1/CDK4 inhibitors: Indolo-[6,7-α]pyrrolo[3,4-c]carbazoles
-
Engler, T. A.; Furness, K.; Malhotra, S.; Sanchez-Martinez, C.; Shih, C.; Xie, W.; Zhu, G.; Zhou, X.; Conner, S.; Faul, M. M.; Sullivan, K. A.; Kolis, S. P.; Brooks, H. B.; Patel, B.; Schultz, R. M.; DeHahn, T. B.; Kirmani, K.; Spencer, C. D.; Watkins, S. A.; Considine, E. L.; Dempsey, J. A.; Ogg, C. A.; Stamm, N. B.; Anderson, B. D.; Campbell, R. M.; Vasudevan, V.; Lytle, M. L. Novel, Potent and Selective Cyclin D1/CDK4 Inhibitors: Indolo-[6,7-α] pyrrolo[3,4-c]carbazoles. Bioorg. Med. Chem. Lett. 2003, 13, 2261-2267.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 2261-2267
-
-
Engler, T.A.1
Furness, K.2
Malhotra, S.3
Sanchez-Martinez, C.4
Shih, C.5
Xie, W.6
Zhu, G.7
Zhou, X.8
Conner, S.9
Faul, M.M.10
Sullivan, K.A.11
Kolis, S.P.12
Brooks, H.B.13
Patel, B.14
Schultz, R.M.15
DeHahn, T.B.16
Kirmani, K.17
Spencer, C.D.18
Watkins, S.A.19
Considine, E.L.20
Dempsey, J.A.21
Ogg, C.A.22
Stamm, N.B.23
Anderson, B.D.24
Campbell, R.M.25
Vasudevan, V.26
Lytle, M.L.27
more..
-
66
-
-
0037424693
-
Synthesis of quinolinyl/isoquinolinyl[α]pyrrolo[3,4-c] carbazoles as cyclin D1/CDK4 inhibitors
-
Zhu, G.; Conner, S.; Zhou, X.; Shih, C.; Brooks, H. B.; Considine, E.; Dempsey, J. A.; Ogg, C.; Patel, B.; Schultz, R. M.; Spencer, C. D.; Teicher, B.; Watkins, S. A. Synthesis of Quinolinyl/Isoquinolinyl[α]pyrrolo[3,4-c] Carbazoles as Cyclin D1/CDK4 Inhibitors. Bioorg. Med. Chem. Lett. 2003, 13, 1231-1235.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1231-1235
-
-
Zhu, G.1
Conner, S.2
Zhou, X.3
Shih, C.4
Brooks, H.B.5
Considine, E.6
Dempsey, J.A.7
Ogg, C.8
Patel, B.9
Schultz, R.M.10
Spencer, C.D.11
Teicher, B.12
Watkins, S.A.13
-
67
-
-
0037573393
-
Synthesis, structure-activity relationship, and biological studies of indolocarbazoles as potent cyclin D1-CDK4 inhibitors
-
Zhu, G.; Conner, S. E.; Zhou, X.; Shih, C.; Li, T.; Anderson, B. D.; Brooks, H. B.; Campbell, R. M.; Considine, E.; Dempsey, J. A.; Faul, M. M.; Ogg, C.; Patel, B.; Schultz, R. M.; Spencer, C. D.; Teicher, B.; Watkins, S. A. Synthesis, Structure-Activity Relationship, and Biological Studies of Indolocarbazoles as Potent Cyclin D1-CDK4 Inhibitors. J. Med. Chem. 2003, 46, 2027-2030.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2027-2030
-
-
Zhu, G.1
Conner, S.E.2
Zhou, X.3
Shih, C.4
Li, T.5
Anderson, B.D.6
Brooks, H.B.7
Campbell, R.M.8
Considine, E.9
Dempsey, J.A.10
Faul, M.M.11
Ogg, C.12
Patel, B.13
Schultz, R.M.14
Spencer, C.D.15
Teicher, B.16
Watkins, S.A.17
-
68
-
-
17944375799
-
Identification of selective inhibitors of cyclin dependent kinase 4
-
Carini, D. J.; Kaltenbach, R. F., III; Liu, J.; Benfield, P. A.; Boylan, J.; Boisclair, M.; Brizuela, L.; Burton, C. R.; Cox, S.; Grafstrom, R.; Harrison, B. A.; Harrison, K.; Akamike, E.; Markwalder, J. A.; Nakano, Y.; Seitz, S. P.; Sharp, D. M.; Trainor, G. L.; Sielecki, T. M. Identification of Selective Inhibitors of Cyclin Dependent Kinase 4. Bioorg. Med. Chem. Lett. 2001, 11, 2209-2211.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2209-2211
-
-
Carini, D.J.1
Kaltenbach III, R.F.2
Liu, J.3
Benfield, P.A.4
Boylan, J.5
Boisclair, M.6
Brizuela, L.7
Burton, C.R.8
Cox, S.9
Grafstrom, R.10
Harrison, B.A.11
Harrison, K.12
Akamike, E.13
Markwalder, J.A.14
Nakano, Y.15
Seitz, S.P.16
Sharp, D.M.17
Trainor, G.L.18
Sielecki, T.M.19
-
69
-
-
0034611440
-
5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents
-
Ryu, C.-K.; Kang, H.-Y.; Lee, S. K.; Nam, K. A.; Hong, C. Y.; Ko, W.-G.; Lee, B.-H. 5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as Inhibitors of Cyclin-Dependent Kinase 4 and Cytotoxic Agents. Bioorg. Med. Chem. Lett. 2000, 10, 461-464.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 461-464
-
-
Ryu, C.-K.1
Kang, H.-Y.2
Lee, S.K.3
Nam, K.A.4
Hong, C.Y.5
Ko, W.-G.6
Lee, B.-H.7
-
70
-
-
0034618674
-
Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product
-
Soni, R.; Muller, L.; Furet, P.; Schoepfer, J.; Stephan, C.; Zumstein-Mecker, S.; Fretz, H.; Chaudhuri, B. Inhibition of Cyclin-Dependent Kinase 4 (Cdk4) by Fascaplysin, a Marine Natural Product. Biochem. Biophys. Res. Commun. 2000, 275, 877-884.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.275
, pp. 877-884
-
-
Soni, R.1
Muller, L.2
Furet, P.3
Schoepfer, J.4
Stephan, C.5
Zumstein-Mecker, S.6
Fretz, H.7
Chaudhuri, B.8
-
71
-
-
0034698889
-
Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1
-
Jeong, H.-W.; Kim, M.-R.; Son, K.-H.; Han, M. Y.; Ha, J.-H.; Garnier, M.; Meijer, L.; Kwon, B.-M. Cinnamaldehydes Inhibit Cyclin Dependent Kinase 4/Cyclin D1. Bioorg. Med. Chem. Lett. 2000, 10, 1819-1822.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1819-1822
-
-
Jeong, H.-W.1
Kim, M.-R.2
Son, K.-H.3
Han, M.Y.4
Ha, J.-H.5
Garnier, M.6
Meijer, L.7
Kwon, B.-M.8
-
72
-
-
0034657527
-
Structure-activity relationship studies of flavopiridol analogues
-
Murthi, K. K.; Dubay, M.; McClure, C.; Brizuela, L.; Boisclair, M. D.; Worland, P. J.; Mansuri, M. M.; Pal, K. Structure-Activity Relationship Studies of Flavopiridol Analogues. Bioorg. Med. Chem. Lett. 2000, 10, 1037-1041.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1037-1041
-
-
Murthi, K.K.1
Dubay, M.2
McClure, C.3
Brizuela, L.4
Boisclair, M.D.5
Worland, P.J.6
Mansuri, M.M.7
Pal, K.8
-
73
-
-
0034597571
-
Thio- and oxoflavopiridols, cyclin-dependeht kinase 1-selective inhibitors: Synthesis and biological effects
-
Kim, K. S.; Sack, J. S.; Tokarski, J. S.; Qian, L.; Chao, S. T.; Leith, L.; Kelly, Y. F.; Misra, R. N.; Hunt, J. T.; Kimball, S. D.; Humphreys, W. G.; Wautlet, B. S.; Mulheron, J. G.; Webster, K. R. Thio- and Oxoflavopiridols, Cyclin-Dependeht Kinase 1-Selective Inhibitors: Synthesis and Biological Effects. J. Med Chem. 2000, 43, 4126-4134.
-
(2000)
J. Med Chem.
, vol.43
, pp. 4126-4134
-
-
Kim, K.S.1
Sack, J.S.2
Tokarski, J.S.3
Qian, L.4
Chao, S.T.5
Leith, L.6
Kelly, Y.F.7
Misra, R.N.8
Hunt, J.T.9
Kimball, S.D.10
Humphreys, W.G.11
Wautlet, B.S.12
Mulheron, J.G.13
Webster, K.R.14
-
74
-
-
0033128165
-
Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases
-
Hoessel, R.; Leclerc, S.; Endicott, J. A.; Nobel, M. E. M.; Lawrie, A.; Tunnah, P.; Loest, M.; Damiens, E.; Marie, D.; Marko, D.; Niederberger, E.; Tang, W.; Eisenbrand, G.; Meijer, L. Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases. Nat. Cell Biol. 1999, 1, 60-67.
-
(1999)
Nat. Cell Biol.
, vol.1
, pp. 60-67
-
-
Hoessel, R.1
Leclerc, S.2
Endicott, J.A.3
Nobel, M.E.M.4
Lawrie, A.5
Tunnah, P.6
Loest, M.7
Damiens, E.8
Marie, D.9
Marko, D.10
Niederberger, E.11
Tang, W.12
Eisenbrand, G.13
Meijer, L.14
-
75
-
-
0034010742
-
Inhibition of cyclin-dependent kinases, GSK-3β and CK1 by hymenialdisine, a marine sponge constituent
-
Meijer, L.; Thunnissen, A.-M. W. H.; White, A. W.; Garnier, M.; Nikolic, M.; Tsai, L.-H.; Walter, J.; Cleverley, K. E.; Salinas, P. C.; Wu, Y.-Z.; Biernat, J.; Mandelkow, E.-M.; Kim, S.-H.; Pettit, G. R. Inhibition of cyclin-dependent kinases, GSK-3β and CK1 by hymenialdisine, a marine sponge constituent. Chem. Biol. 2000, 7, 51-63.
-
(2000)
Chem. Biol.
, vol.7
, pp. 51-63
-
-
Meijer, L.1
Thunnissen, A.-M.W.H.2
White, A.W.3
Garnier, M.4
Nikolic, M.5
Tsai, L.-H.6
Walter, J.7
Cleverley, K.E.8
Salinas, P.C.9
Wu, Y.-Z.10
Biernat, J.11
Mandelkow, E.-M.12
Kim, S.-H.13
Pettit, G.R.14
-
76
-
-
17144407039
-
The in vitro and in vivo effects of small molecule inhibitors of cyclin dependent kinase 4
-
Mar 27-31, Orlando, FL, Abstract #3126
-
DePinto, W. E.; Yin, X.; Smith, M.; Kolinsky, K.; Desai, B.; Rowan, K.; Wang, K.; Perrotta, A.; Gillespie, P. The In Vitro and In Vivo Effects of Small Molecule Inhibitors of Cyclin Dependent Kinase 4. Presented at the American Association of Cancer Research 95th Annual National Meeting, Mar 27-31, 2003, Orlando, FL, Abstract #3126.
-
(2003)
American Association of Cancer Research 95th Annual National Meeting
-
-
DePinto, W.E.1
Yin, X.2
Smith, M.3
Kolinsky, K.4
Desai, B.5
Rowan, K.6
Wang, K.7
Perrotta, A.8
Gillespie, P.9
-
77
-
-
0034736093
-
Pyrido-[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases
-
Barvian, M.; Boschelli, D. H.; Cossrow, J.; Dobrusin, E.; Fattaey, A.; Fritsch, A.; Fry, D.; Harvey P.; Keller, P.; Garrett, M.; La, F.; Leopold, W.; McNamara, D.; Quin, M.; Trumpp-Kallmeyer, S.; Toogood, P.; Wu, Z.; Zhang, E. Pyrido-[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases. J. Med. Chem. 2000, 43, 4606-4616.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4606-4616
-
-
Barvian, M.1
Boschelli, D.H.2
Cossrow, J.3
Dobrusin, E.4
Fattaey, A.5
Fritsch, A.6
Fry, D.7
Harvey, P.8
Keller, P.9
Garrett, M.10
La, F.11
Leopold, W.12
McNamara, D.13
Quin, M.14
Trumpp-Kallmeyer, S.15
Toogood, P.16
Wu, Z.17
Zhang, E.18
-
78
-
-
0035907260
-
Cell cycle and biochemical effects of PD 0183812. A potent inhibitor of the cyclin D-dependent kinases CDK4 and CDK6
-
Fry, D. W.; Bedford, D. C.; Harvey, P. H.; Fritsch, A.; Keller, P. R.; Wu, Z.; Dobrusin, E.; Leopold, W. R.; Fattaey, A.; Garrett, M. D. Cell cycle and biochemical effects of PD 0183812. A potent inhibitor of the cyclin D-dependent kinases CDK4 and CDK6. J. Biol. Chem. 2001, 276, 16617-16623.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 16617-16623
-
-
Fry, D.W.1
Bedford, D.C.2
Harvey, P.H.3
Fritsch, A.4
Keller, P.R.5
Wu, Z.6
Dobrusin, E.7
Leopold, W.R.8
Fattaey, A.9
Garrett, M.D.10
-
79
-
-
0034800665
-
Cyclin-dependent kinase inhibitors for treating cancer
-
Toogood, P. L. Cyclin-Dependent Kinase Inhibitors for Treating Cancer. Med. Res. Rev. 2001, 21, 487-498.
-
(2001)
Med. Res. Rev.
, vol.21
, pp. 487-498
-
-
Toogood, P.L.1
-
80
-
-
0344809977
-
ATP-site directed inhibitors of cyclin-dependent kinases
-
Gray, N.; Détivaud, L.; Doerig, C.; Meijer, K. ATP-Site Directed Inhibitors of cyclin-Dependent Kinases. Curr. Med. Chem. 1999, 6, 859-875.
-
(1999)
Curr. Med. Chem.
, vol.6
, pp. 859-875
-
-
Gray, N.1
Détivaud, L.2
Doerig, C.3
Meijer, K.4
-
81
-
-
0041807380
-
-
Griffith, W. P.; Ley, S. V.; Whitcombe, G. P.; White, A. D. J. Chem. Soc., Chem. Commun. 1987, 1625.
-
(1987)
Chem. Soc., Chem. Commun.
, pp. 1625
-
-
Griffith, W.P.1
Ley, S.V.2
Whitcombe, G.P.3
White, A.D.J.4
-
83
-
-
0001158422
-
Reaction of (trifluoromethyl)trimethylsilane with oxazolidin-5-ones: Synthesis of peptidic and nonpeptidic trifluoromethyl ketones
-
Walter, M. W.; Adlington, R. M.; Baldwin, J. E.; Schofield, C. J. Reaction of (Trifluoromethyl)trimethylsilane with Oxazolidin-5-ones: Synthesis of Peptidic and Nonpeptidic Trifluoromethyl Ketones J. Org. Chem. 1998, 63, 5179-5192.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 5179-5192
-
-
Walter, M.W.1
Adlington, R.M.2
Baldwin, J.E.3
Schofield, C.J.4
-
84
-
-
33644528891
-
Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
-
Dess, D. B.; Martin, J. C. Readily Accessible 12-I-5 Oxidant for the Conversion of Primary and Secondary Alcohols to Aldehydes and Ketones. J. Org. Chem. 1983, 48, 4155-4156.
-
(1983)
J. Org. Chem.
, vol.48
, pp. 4155-4156
-
-
Dess, D.B.1
Martin, J.C.2
-
85
-
-
33845553416
-
Chemistry of oxaziridines. 2. Improved synthesis of 2- sulfonyloxaziridines
-
Davis, F. A.; Stringer, O. D. Chemistry of Oxaziridines. 2. Improved Synthesis of 2-Sulfonyloxaziridines. J. Org. Chem. 1982, 47, 1774-1775.
-
(1982)
J. Org. Chem.
, vol.47
, pp. 1774-1775
-
-
Davis, F.A.1
Stringer, O.D.2
-
86
-
-
33845554384
-
Chemistry of oxaziridines. 3. Asymmetric oxidation of organosulfur compounds using chiral 2-sulfonyloxaziridines
-
Davis, F. A.; Jenkins, R. H., Jr; Awad, S. B.; Stringer, O. D.; Watson, W. H.; Galloy, J. Chemistry of Oxaziridines. 3. Asymmetric Oxidation of Organosulfur Compounds Using Chiral 2-Sulfonyloxaziridines. J. Am. Chem. Soc. 1982,104, 5412-5418.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 5412-5418
-
-
Davis, F.A.1
Jenkins Jr., R.H.2
Awad, S.B.3
Stringer, O.D.4
Watson, W.H.5
Galloy, J.6
-
87
-
-
20244365948
-
Discovery of a potent and selective inhibitor of cyclin-dependent kinase 4/6
-
Toodgood, P. L.; Harvey, P. J.; Repine, J. T.; Sheehan, D. J.; VanderWel, S. N.; Zhou, H.; Keller, P. R.; McNamara, D. J.; Sherry, D.; Zhu, T.; Brodfuehrer, J.; Choi, C.; Barvian, M. R.; Fry, D. W. Discovery of a Potent and Selective Inhibitor of Cyclin-Dependent Kinase 4/6. J. Med. Chem. 2005, 48, 2388-2406.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2388-2406
-
-
Toodgood, P.L.1
Harvey, P.J.2
Repine, J.T.3
Sheehan, D.J.4
VanderWel, S.N.5
Zhou, H.6
Keller, P.R.7
McNamara, D.J.8
Sherry, D.9
Zhu, T.10
Brodfuehrer, J.11
Choi, C.12
Barvian, M.R.13
Fry, D.W.14
|