-
1
-
-
0344809977
-
ATP-site directed inhibitors of cyclin-dependent kinases
-
Gray, N.; Detivaud, L.; Doerig, C.; Meijer, L. 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
Detivaud, L.2
Doerig, C.3
Meijer, L.4
-
2
-
-
80052499578
-
Cyclin-dependent kinases: Bridging their structure and function through computations
-
De Vivo, M.; Bottegoni, G.; Berteotti, A.; Recanatini, M.; Gervasio, F.L.; Cavalli, A. Cyclin-dependent kinases: Bridging their structure and function through computations. Future Med. Chem. 2011, 3, 1551–1559.
-
(2011)
Future Med. Chem
, vol.3
, pp. 1551-1559
-
-
De Vivo, M.1
Bottegoni, G.2
Berteotti, A.3
Recanatini, M.4
Gervasio, F.L.5
Cavalli, A.6
-
3
-
-
77958587420
-
CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1
-
Bartkowiak, B.; Liu, P.; Phatnani, H.P.; Fuda, N.J.; Cooper, J.J.; Price, D.H.; Adelman, K.; Lis, J.T.; Greenleaf, A.L. CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1. Genes Dev. 2010, 24, 2303–2316.
-
(2010)
Genes Dev
, vol.24
, pp. 2303-2316
-
-
Bartkowiak, B.1
Liu, P.2
Phatnani, H.P.3
Fuda, N.J.4
Cooper, J.J.5
Price, D.H.6
Adelman, K.7
Lis, J.T.8
Greenleaf, A.L.9
-
4
-
-
0036181669
-
Designing inhibitors of cyclin-dependent kinases. Annu
-
Hardcastle, I.R.; Golding, B.T.; Griffin, R.J. Designing inhibitors of cyclin-dependent kinases. Annu. Rev. Pharmacol. Toxicol. 2002, 42, 325–348.
-
(2002)
Rev. Pharmacol. Toxicol
, vol.42
, pp. 325-348
-
-
Hardcastle, I.R.1
Golding, B.T.2
Griffin, R.J.3
-
5
-
-
25444444192
-
CAK-Cyclin-dependent Activating Kinase: A key kinase in cell cycle control and a target for drugs?
-
Lolli, G.; Johnson, L.N. CAK-Cyclin-dependent Activating Kinase: A key kinase in cell cycle control and a target for drugs? Cell Cycle 2005, 4, 572–577.
-
(2005)
Cell Cycle
, vol.4
, pp. 572-577
-
-
Lolli, G.1
Johnson, L.N.2
-
6
-
-
0029029617
-
Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex
-
Jeffrey, P.D.; Russo, A.A.; Polyak, K.; Gibbs, E.; Hurwitz, J.; Massague, J.; Pavletich, N.P. Mechanism of CDK activation revealed by the structure of a cyclinA-CDK2 complex. Nature 1995, 376, 313–320.
-
(1995)
Nature
, vol.376
, pp. 313-320
-
-
Jeffrey, P.D.1
Russo, A.A.2
Polyak, K.3
Gibbs, E.4
Hurwitz, J.5
Massague, J.6
Pavletich, N.P.7
-
7
-
-
33947424005
-
Fisher, R.P. Requirements for CDK7 in the assembly of CDK1/cyclin B and activation of CDK2 revealed by chemical genetics in human cells. Mol
-
Larochelle, S.; Merrick, K.A.; Terret, M.E.; Wohlbold, L.; Barboza, N.M.; Zhang, C.; Shokat, K.M.; Jallepalli, P.V.; Fisher, R.P. Requirements for CDK7 in the assembly of CDK1/cyclin B and activation of CDK2 revealed by chemical genetics in human cells. Mol. Cell 2007, 25, 839–850.
-
(2007)
Cell
, vol.25
, pp. 839-850
-
-
Larochelle, S.1
Merrick, K.A.2
Terret, M.E.3
Wohlbold, L.4
Barboza, N.M.5
Zhang, C.6
Shokat, K.M.7
Jallepalli, P.V.8
-
8
-
-
79953232778
-
A novel PKC-ι inhibitor abrogates cell proliferation and induces apoptosis in neuroblastoma
-
Pillai, P.; Desai, S.; Patel, R.; Sajan, M.; Farese, R.; Ostrov, D.; Acevedo-Duncan, M. A novel PKC-ι inhibitor abrogates cell proliferation and induces apoptosis in neuroblastoma. Int. J. Biochem. Cell Biol. 2011, 43, 784–794.
-
(2011)
Int. J. Biochem. Cell Biol
, vol.43
, pp. 784-794
-
-
Pillai, P.1
Desai, S.2
Patel, R.3
Sajan, M.4
Farese, R.5
Ostrov, D.6
Acevedo-Duncan, M.7
-
9
-
-
79951725943
-
Cell cycle arrest in cultured neuroblastoma cells exposed to a bis(Thiosemicarbazonato) metal complex
-
Bica, L.; Meyerowitz, J.; Parker, S.J.; Caragounis, A.; Du, T.; Paterson, B.M.; Barnham, K.J.; Crouch, P.J.; White, A.R.; Donnelly, P.S. Cell cycle arrest in cultured neuroblastoma cells exposed to a bis(thiosemicarbazonato) metal complex. Biometals 2011, 24, 117–133.
-
(2011)
Biometals
, vol.24
, pp. 117-133
-
-
Bica, L.1
Meyerowitz, J.2
Parker, S.J.3
Caragounis, A.4
Du, T.5
Paterson, B.M.6
Barnham, K.J.7
Crouch, P.J.8
White, A.R.9
Donnelly, P.S.10
-
10
-
-
0027994603
-
A novel cyclin associates with MO15/CDK7 to form the CDK-activating kinase
-
Fisher, R.P.; Morgan, D.O. A novel cyclin associates with MO15/CDK7 to form the CDK-activating kinase. Cell 1994, 78, 713–724.
-
(1994)
Cell
, vol.78
, pp. 713-724
-
-
Fisher, R.P.1
Morgan, D.O.2
-
11
-
-
0033574614
-
Mechanisms of cyclin-dependent kinase regulation: Structures of cdks, their cyclin activators, and cip and INK4 inhibitors
-
Pavletich, N.P. Mechanisms of cyclin-dependent kinase regulation: Structures of cdks, their cyclin activators, and cip and INK4 inhibitors. J. Mol. Biol. 1999, 287, 821–828.
-
(1999)
J. Mol. Biol
, vol.287
, pp. 821-828
-
-
Pavletich, N.P.1
-
12
-
-
0033954256
-
The protein data bank
-
Berman, H.M.; Westbrook, J.; Feng, Z.; Gilliland, G.; Bhat, T.N.; Weissig, H.; Shindyalov, I.N.; Bourne, P.E. The protein data bank. Nucleic Acids Res. 2000, 28, 235–242.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 235-242
-
-
Berman, H.M.1
Westbrook, J.2
Feng, Z.3
Gilliland, G.4
Bhat, T.N.5
Weissig, H.6
Shindyalov, I.N.7
Bourne, P.E.8
-
13
-
-
33645802169
-
Cyclin-dependent kinase pathways as targets for cancer treatment
-
Shapiro, G.I. Cyclin-dependent kinase pathways as targets for cancer treatment. J. Clin. Oncol. 2006, 24, 1770–1783.
-
(2006)
J. Clin. Oncol
, vol.24
, pp. 1770-1783
-
-
Shapiro, G.I.1
-
15
-
-
0026176336
-
Cyclins: Wheels within wheels
-
Pines, J. Cyclins: Wheels within wheels. Cell Growth Differ. 1991, 2, 305–310.
-
(1991)
Cell Growth Differ
, vol.2
, pp. 305-310
-
-
Pines, J.1
-
16
-
-
0032854118
-
The structure-based design of ATP-site directed protein kinase inhibitors
-
Toledo, L.M.; Lydon, N.B.; Elbaum, D. The structure-based design of ATP-site directed protein kinase inhibitors. Curr. Med. Chem. 1999, 6, 775–805.
-
(1999)
Curr. Med. Chem
, vol.6
, pp. 775-805
-
-
Toledo, L.M.1
Lydon, N.B.2
Elbaum, D.3
-
17
-
-
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
-
18
-
-
77149140115
-
Nuclear targeting of cyclin-dependent kinase 2 reveals essential roles of cyclin-dependent kinase 2 localization and cyclin
-
Flores, O.; Wang, Z.; Knudsen, K.E.; Burnstein, K.L. Nuclear targeting of cyclin-dependent kinase 2 reveals essential roles of cyclin-dependent kinase 2 localization and cyclin E in vitamin D-mediated growth inhibition. Endocrinology 2010, 151, 896–908.
-
(2010)
E in Vitamin D-Mediated Growth Inhibition. Endocrinology
, vol.151
, pp. 896-908
-
-
Flores, O.1
Wang, Z.2
Knudsen, K.E.3
Burnstein, K.L.4
-
19
-
-
0031596172
-
Role of p27Kip1 and cyclin-dependent kinase 2 in the proliferation of non-small cell lung cancer
-
Kawana, H.; Tamaru, J.-I.; Tanaka, T.; Hirai, A.; Saito, Y.; Kitagawa, M.; Mikata, A.; Harigaya, K.; Kuriyama, T. Role of p27Kip1 and cyclin-dependent kinase 2 in the proliferation of non-small cell lung cancer. Am. J. Pathol. 1998, 153, 505–513.
-
(1998)
Am. J. Pathol
, vol.153
, pp. 505-513
-
-
Kawana, H.1
Tamaru, J.-I.2
Tanaka, T.3
Hirai, A.4
Saito, Y.5
Kitagawa, M.6
Mikata, A.7
Harigaya, K.8
Kuriyama, T.9
-
20
-
-
68049125103
-
The development of a selective cyclin-dependent kinase inhibitor that shows antitumor activity
-
Ali, S.; Heathcote, D.A.; Kroll, S.H.; Jogalekar, A.S.; Scheiper, B.; Patel, H.; Brackow, J.; Siwicka, A.; Fuchter, M.J.; Periyasamy, M. The development of a selective cyclin-dependent kinase inhibitor that shows antitumor activity. Cancer Res. 2009, 69, 6208–6215.
-
(2009)
Cancer Res
, vol.69
, pp. 6208-6215
-
-
Ali, S.1
Heathcote, D.A.2
Kroll, S.H.3
Jogalekar, A.S.4
Scheiper, B.5
Patel, H.6
Brackow, J.7
Siwicka, A.8
Fuchter, M.J.9
Periyasamy, M.10
-
21
-
-
75549090821
-
Pre-clinical evaluation of cyclin-dependent kinase 2 and 1 inhibition in anti-estrogen-sensitive and resistant breast cancer cells
-
Johnson, N.; Bentley, J.; Wang, L.; Newell, D.; Robson, C.; Shapiro, G.; Curtin, N. Pre-clinical evaluation of cyclin-dependent kinase 2 and 1 inhibition in anti-estrogen-sensitive and resistant breast cancer cells. Br. J. Cancer 2009, 102, 342–350.
-
(2009)
Br. J. Cancer
, vol.102
, pp. 342-350
-
-
Johnson, N.1
Bentley, J.2
Wang, L.3
Newell, D.4
Robson, C.5
Shapiro, G.6
Curtin, N.7
-
23
-
-
84881361773
-
Anticancer therapeutic strategies based on CDK inhibitors
-
Esposito, L.; Indovina, P.; Magnotti, F.; Conti, D.; Giordano, A. Anticancer therapeutic strategies based on CDK inhibitors. Curr. Pharm. Des. 2013, 19, 5327–5332.
-
(2013)
Curr. Pharm. Des
, vol.19
, pp. 5327-5332
-
-
Esposito, L.1
Indovina, P.2
Magnotti, F.3
Conti, D.4
Giordano, A.5
-
24
-
-
37549036250
-
Inhibitors in cancer therapy: What is next?
-
Malumbres, M.; Pevarello, P.; Barbacid, M.; Bischoff, J.R. CDK inhibitors in cancer therapy: What is next? Trends Pharmacol. Sci. 2008, 29, 16–21.
-
(2008)
Trends Pharmacol. Sci
, vol.29
, pp. 16-21
-
-
Malumbres, M.1
Pevarello, P.2
Barbacid, M.3
Bischoff, J.4
-
25
-
-
33750469601
-
In vitro and in vivo activity of R547: A potent and selective cyclin-dependent kinase inhibitor currently in phase I clinical trials
-
DePinto, W.; Chu, X.J.; Yin, X.; Smith, M.; Packman, K.; Goelzer, P.; Lovey, A.; Chen, Y.; Qian, H.; Hamid, R, et al. In vitro and in vivo activity of R547: A potent and selective cyclin-dependent kinase inhibitor currently in phase I clinical trials. Mol. Cancer Ther. 2006, 5, 2644–2658.
-
(2006)
Mol. Cancer Ther
, vol.5
, pp. 2644-2658
-
-
Depinto, W.1
Chu, X.J.2
Yin, X.3
Smith, M.4
Packman, K.5
Goelzer, P.6
Lovey, A.7
Chen, Y.8
Qian, H.9
Hamid, R.10
-
26
-
-
20444477948
-
Seliciclib (CYC202, R-Roscovitine) induces cell death in multiple myeloma cells by inhibition of RNA polymerase II-dependent transcription and down-regulation of Mcl-1
-
MacCallum, D.E.; Melville, J.; Frame, S.; Watt, K.; Anderson, S.; Gianella-Borradori, A.; Lane, D.P.; Green, S.R. Seliciclib (CYC202, R-Roscovitine) induces cell death in multiple myeloma cells by inhibition of RNA polymerase II-dependent transcription and down-regulation of Mcl-1. Cancer Res. 2005, 65, 5399–5407.
-
(2005)
Cancer Res
, vol.65
, pp. 5399-5407
-
-
Maccallum, D.E.1
Melville, J.2
Frame, S.3
Watt, K.4
Anderson, S.5
Gianella-Borradori, A.6
Lane, D.P.7
Green, S.R.8
-
27
-
-
77950837310
-
Inhibitors: From the bench to clinical trials
-
Rizzolio, F.; Tuccinardi, T.; Caligiuri, I.; Lucchetti, C.; Giordano, A. CDK inhibitors: From the bench to clinical trials. Curr. Drug Targets 2010, 11, 279–290.
-
(2010)
Curr. Drug Targets
, vol.11
, pp. 279-290
-
-
Rizzolio, F.1
Tuccinardi, T.2
Caligiuri, I.3
Lucchetti, C.4
Giordano, A.5
-
28
-
-
84867493189
-
P276–00, a cyclin-dependent kinase inhibitor, modulates cell cycle and induces apoptosis in vitro and in vivo in mantle cell lymphoma cell lines
-
Shirsath, N.P.; Manohar, S.M.; Joshi, K.S. P276–00, a cyclin-dependent kinase inhibitor, modulates cell cycle and induces apoptosis in vitro and in vivo in mantle cell lymphoma cell lines. Mol. Cancer 2012, 11, 77, doi:10.1186/1476-4598-11-77.
-
(2012)
Mol. Cancer
, vol.11
, pp. 77
-
-
Shirsath, N.P.1
Manohar, S.M.2
Joshi, K.S.3
-
29
-
-
80053603444
-
Induction of eosinophil apoptosis by the cyclin-dependent kinase inhibitor AT7519 promotes the resolution of eosinophil-dominant allergic inflammation
-
Alessandri, A.L.; Duffin, R.; Leitch, A.E.; Lucas, C.D.; Sheldrake, T.A.; Dorward, D.A.; Hirani, N.; Pinho, V.; de Sousa, L.P.; Teixeira, M.M, et al. Induction of eosinophil apoptosis by the cyclin-dependent kinase inhibitor AT7519 promotes the resolution of eosinophil-dominant allergic inflammation. PLoS ONE 2011, 6, e25683.
-
(2011)
Plos ONE
, vol.6
-
-
Alessandri, A.L.1
Duffin, R.2
Leitch, A.E.3
Lucas, C.D.4
Sheldrake, T.A.5
Dorward, D.A.6
Hirani, N.7
Pinho, V.8
De Sousa, L.P.9
Teixeira, M.M.10
-
30
-
-
36849021157
-
Therapeutic potential of CDK inhibitor NU2058 in androgen-independent prostate cancer
-
Rigas, A.C.; Robson, C.N.; Curtin, N.J. Therapeutic potential of CDK inhibitor NU2058 in androgen-independent prostate cancer. Oncogene 2007, 26, 7611–7619.
-
(2007)
Oncogene
, vol.26
, pp. 7611-7619
-
-
Rigas, A.C.1
Robson, C.N.2
Curtin, N.J.3
-
31
-
-
80054752304
-
The CDK inhibitors in cancer research and therapy
-
Cicenas, J.; Valius, M. The CDK inhibitors in cancer research and therapy. J. Cancer Res. Clin. Oncol. 2011, 137, 1409–1418.
-
(2011)
J. Cancer Res. Clin. Oncol
, vol.137
, pp. 1409-1418
-
-
Cicenas, J.1
Valius, M.2
-
32
-
-
34147127727
-
In vitro antitumor properties of a novel cyclin-dependent kinase inhibitor, P276–00. Mol
-
Joshi, K.S.; Rathos, M.J.; Joshi, R.D.; Sivakumar, M.; Mascarenhas, M.; Kamble, S.; Lal, B.; Sharma, S. In vitro antitumor properties of a novel cyclin-dependent kinase inhibitor, P276–00. Mol. Cancer Ther. 2007, 6, 918–925.
-
(2007)
Cancer Ther
, vol.6
, pp. 918-925
-
-
Joshi, K.S.1
Rathos, M.J.2
Joshi, R.D.3
Sivakumar, M.4
Mascarenhas, M.5
Kamble, S.6
Lal, B.7
Sharma, S.8
-
33
-
-
34147167723
-
P276–00, a novel cyclin-dependent inhibitor induces G1-G2 arrest, shows antitumor activity on cisplatin-resistant cells and significant in vivo efficacy in tumor models
-
Joshi, K.S.; Rathos, M.J.; Mahajan, P.; Wagh, V.; Shenoy, S.; Bhatia, D.; Chile, S.; Sivakumar, M.; Maier, A.; Fiebig, H.H, et al. P276–00, a novel cyclin-dependent inhibitor induces G1-G2 arrest, shows antitumor activity on cisplatin-resistant cells and significant in vivo efficacy in tumor models. Mol. Cancer Ther. 2007, 6, 926–934.
-
(2007)
Mol. Cancer Ther
, vol.6
, pp. 926-934
-
-
Joshi, K.S.1
Rathos, M.J.2
Mahajan, P.3
Wagh, V.4
Shenoy, S.5
Bhatia, D.6
Chile, S.7
Sivakumar, M.8
Maier, A.9
Fiebig, H.H.10
-
34
-
-
0031028163
-
Inhibition of cyclin-dependent kinases by purine analogues: Crystal structure of human cdk2 complexed with roscovitine
-
De Azevedo, W.F.; Leclerc, S.; Meijer, L.; Havlicek, L.; Strnad, M.; Kim, S.H. Inhibition of cyclin-dependent kinases by purine analogues: Crystal structure of human cdk2 complexed with roscovitine. Eur. J. Biochem. 1997, 243, 518–526.
-
(1997)
Eur. J. Biochem
, vol.243
, pp. 518-526
-
-
De Azevedo, W.F.1
Leclerc, S.2
Meijer, L.3
Havlicek, L.4
Strnad, M.5
Kim, S.H.6
-
35
-
-
33947498211
-
A small molecule based on the pRb2/p130 spacer domain leads to inhibition of cdk2 activity, cell cycle arrest and tumor growth reduction in vivo
-
Bagella, L.; Sun, A.; Tonini, T.; Abbadessa, G.; Cottone, G.; Paggi, M.G.; de Luca, A.; Claudio, P.P.; Giordano, A. A small molecule based on the pRb2/p130 spacer domain leads to inhibition of cdk2 activity, cell cycle arrest and tumor growth reduction in vivo. Oncogene 2007, 26, 1829–1839.
-
(2007)
Oncogene
, vol.26
, pp. 1829-1839
-
-
Bagella, L.1
Sun, A.2
Tonini, T.3
Abbadessa, G.4
Cottone, G.5
Paggi, M.G.6
De Luca, A.7
Claudio, P.P.8
Giordano, A.9
-
36
-
-
84880564100
-
Structural characterization of the cyclin-dependent protein kinase family
-
Endicott, J.A.; Noble, M.E. Structural characterization of the cyclin-dependent protein kinase family. Biochem. Soc. Trans. 2013, 41, 1008–1016.
-
(2013)
Biochem. Soc. Trans
, vol.41
, pp. 1008-1016
-
-
Endicott, J.A.1
Noble, M.E.2
-
37
-
-
0026452974
-
Growth inhibition with reversible cell cycle arrest of carcinoma cells by flavone L86–8275
-
Kaur, G.; Stetler-Stevenson, M.; Sebers, S.; Worland, P.; Sedlacek, H.; Myers, C.; Czech, J.; Naik, R.; Sausville, E. Growth inhibition with reversible cell cycle arrest of carcinoma cells by flavone L86–8275. J. Natl. Cancer Inst. 1992, 84, 1736–1740.
-
(1992)
J. Natl. Cancer Inst
, vol.84
, pp. 1736-1740
-
-
Kaur, G.1
Stetler-Stevenson, M.2
Sebers, S.3
Worland, P.4
Sedlacek, H.5
Myers, C.6
Czech, J.7
Naik, R.8
Sausville, E.9
-
38
-
-
0029993339
-
Structural basis for specificity and potency of a flavonoid inhibitor of human CDK2, a cell cycle kinase
-
De Azevedo, W., Jr; Mueller-Dieckmann, H.; Schulze-Gahmen, U.; Worland, P.; Sausville, E.; Kim, S. Structural basis for specificity and potency of a flavonoid inhibitor of human CDK2, a cell cycle kinase. Proc. Natl. Acad. Sci. USA 1996, 93, 2735–2740.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 2735-2740
-
-
De Azevedo, W.1
Mueller-Dieckmann, H.2
Schulze-Gahmen, U.3
Worland, P.4
Sausville, E.5
Kim, S.6
-
39
-
-
0034657527
-
Structure-activity relationship studies of flavopiridol analogues. Bioorg. Med
-
Murthi, K.; Dubay, M.; McClure, C.; Brizuela, L.; Boisclair, M.; Worland, P.; Mansuri, M.; Pal, K. Structure-activity relationship studies of flavopiridol analogues. Bioorg. Med. Chem. Lett. 2000, 10, 1037–1041.
-
(2000)
Chem. Lett
, vol.10
, pp. 1037-1041
-
-
Murthi, K.1
Dubay, M.2
McClure, C.3
Brizuela, L.4
Boisclair, M.5
Worland, P.6
Mansuri, M.7
Pal, K.8
-
40
-
-
0037058678
-
In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R-roscovitine)
-
McClue, S.; Blake, D.; Clarke, R.; Cowan, A.; Cummings, L.; Fischer, P.; MacKenzie, M.; Melville, J.; Stewart, K.; Wang, S. 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.1
Blake, D.2
Clarke, R.3
Cowan, A.4
Cummings, L.5
Fischer, P.6
Mackenzie, M.7
Melville, J.8
Stewart, K.9
Wang, S.10
-
41
-
-
0031037714
-
Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5
-
Meijer, L.; Borgne, A.; Mulner, O.; Chong, J.; Blow, J.; Inagaki, N.; Inagaki, M.; Delcros, J.; Moulinoux, J. Biochemical and cellular effects of roscovitine, a potent and selective inhibitor 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.4
Blow, J.5
Inagaki, N.6
Inagaki, M.7
Delcros, J.8
Moulinoux, J.9
-
42
-
-
77950630091
-
The cyclin-dependent kinase inhibitor PHA-848125 suppresses the in vitro growth of human melanomas sensitive or resistant to temozolomide, and shows synergistic effects in combination with this triazene compound
-
Caporali, S.; Alvino, E.; Starace, G.; Ciomei, M.; Brasca, M.; Levati, L.; Garbin, A.; Castiglia, D.; Covaciu, C.; Bonmassar, E. The cyclin-dependent kinase inhibitor PHA-848125 suppresses the in vitro growth of human melanomas sensitive or resistant to temozolomide, and shows synergistic effects in combination with this triazene compound. Pharmacol. Res. 2010, 61, 437–448.
-
(2010)
Pharmacol. Res
, vol.61
, pp. 437-448
-
-
Caporali, S.1
Alvino, E.2
Starace, G.3
Ciomei, M.4
Brasca, M.5
Levati, L.6
Garbin, A.7
Castiglia, D.8
Covaciu, C.9
Bonmassar, E.10
-
43
-
-
0029871688
-
UCN-01, 7-hydroxyl-staurosporine, inhibits kinase activity of cyclin-dependent kinases and reduces the phosphorylation of the retinoblastoma susceptibility gene product in A549 human lung cancer cell line
-
Kawakami, K.; Futami, H.; Takahara, J.; Yamaguchi, K. UCN-01, 7-hydroxyl-staurosporine, inhibits kinase activity of cyclin-dependent kinases and reduces the phosphorylation of the retinoblastoma susceptibility gene product in A549 human lung cancer cell line. Biochem. Biophys. Res. Commun. 1996, 219, 778–783.
-
(1996)
Biochem. Biophys. Res. Commun
, vol.219
, pp. 778-783
-
-
Kawakami, K.1
Futami, H.2
Takahara, J.3
Yamaguchi, K.4
-
44
-
-
84861547375
-
A phase II study of cell cycle inhibitor UCN-01 in patients with metastatic melanoma: A California Cancer Consortium trial
-
Li, T.; Christensen, S.; Frankel, P.; Margolin, K.; Agarwala, S.; Luu, T.; Mack, P.; Lara, P., Jr.; Gandara, D. A phase II study of cell cycle inhibitor UCN-01 in patients with metastatic melanoma: A California Cancer Consortium trial. Investig. New Drugs 2012, 30, 741–748.
-
(2012)
Investig. New Drugs
, vol.30
, pp. 741-748
-
-
Li, T.1
Christensen, S.2
Frankel, P.3
Margolin, K.4
Agarwala, S.5
Luu, T.6
Mack, P.7
Lara, P.8
Gandara, D.9
-
45
-
-
0036057475
-
The cell cycle as a target for cancer therapy: Basic and clinical findings with the small molecule inhibitors flavopiridol and UCN-01
-
Senderowicz, A. The cell cycle as a target for cancer therapy: Basic and clinical findings with the small molecule inhibitors flavopiridol and UCN-01. Oncologist 2002, 7, 12–19.
-
(2002)
Oncologist
, vol.7
, pp. 12-19
-
-
Senderowicz, A.1
-
46
-
-
33750429279
-
Discovery of (4-Amino-2-(1-methanesulfonylpiperidin-4-ylamino) pyrimidin-5-yl)(2, 3-difluoro-6-methoxyphenyl) methanone (R547), a potent and selective cyclin-dependent kinase inhibitor with significant in vivo antitumor activity
-
Chu, X.; DePinto, W.; Bartkovitz, D.; So, S.; Vu, B.; Packman, K.; Lukacs, C.; Ding, Q.; Jiang, N.; Wang, K. Discovery of (4-Amino-2-(1-methanesulfonylpiperidin-4-ylamino) pyrimidin-5-yl)(2, 3-difluoro-6-methoxyphenyl) methanone (R547), a potent and selective cyclin-dependent kinase inhibitor with significant in vivo antitumor activity. J. Med. Chem. 2006, 49, 6549–6560.
-
(2006)
J. Med. Chem
, vol.49
, pp. 6549-6560
-
-
Chu, X.1
Depinto, W.2
Bartkovitz, D.3
So, S.4
Vu, B.5
Packman, K.6
Lukacs, C.7
Ding, Q.8
Jiang, N.9
Wang, K.10
-
47
-
-
80052396603
-
A phase I pharmacokinetic and pharmacodynamic study of AT7519, a cyclin-dependent kinase inhibitor in patients with refractory solid tumors
-
Mahadevan, D.; Plummer, R.; Squires, M.; Rensvold, D.; Kurtin, S.; Pretzinger, C.; Dragovich, T.; Adams, J.; Lock, V.; Smith, D. A phase I pharmacokinetic and pharmacodynamic study of AT7519, a cyclin-dependent kinase inhibitor in patients with refractory solid tumors. Ann. Oncol. 2011, 22, 2137–2143.
-
(2011)
Ann. Oncol
, vol.22
, pp. 2137-2143
-
-
Mahadevan, D.1
Plummer, R.2
Squires, M.3
Rensvold, D.4
Kurtin, S.5
Pretzinger, C.6
Dragovich, T.7
Adams, J.8
Lock, V.9
Smith, D.10
-
48
-
-
77950825064
-
AT7519, a cyclin-dependent kinase inhibitor, exerts its effects by transcriptional inhibition in leukemia cell lines and patient samples
-
Squires, M.S.; Cooke, L.; Lock, V.; Qi, W.; Lewis, E.J.; Thompson, N.T.; Lyons, J.F.; Mahadevan, D. AT7519, a cyclin-dependent kinase inhibitor, exerts its effects by transcriptional inhibition in leukemia cell lines and patient samples. Mol. Cancer Ther. 2010, 9, 920–928.
-
(2010)
Mol. Cancer Ther
, vol.9
, pp. 920-928
-
-
Squires, M.S.1
Cooke, L.2
Lock, V.3
Qi, W.4
Lewis, E.J.5
Thompson, N.T.6
Lyons, J.F.7
Mahadevan, D.8
-
49
-
-
84882602512
-
Chronic lymphocytic leukemia: 2013 update on diagnosis, risk stratification and treatment
-
Hallek, M. Chronic lymphocytic leukemia: 2013 update on diagnosis, risk stratification and treatment. Am. J. Hematol. 2013, 88, 803–816.
-
(2013)
Am. J. Hematol
, vol.88
, pp. 803-816
-
-
Hallek, M.1
-
50
-
-
77955485400
-
Dinaciclib (SCH 727965), a novel and potent cyclin-dependent kinase inhibitor
-
Parry, D.; Guzi, T.; Shanahan, F.; Davis, N.; Prabhavalkar, D.; Wiswell, D.; Seghezzi, W.; Paruch, K.; Dwyer, M.P.; Doll, R, et al. Dinaciclib (SCH 727965), a novel and potent cyclin-dependent kinase inhibitor. Mol. Cancer Ther. 2010, 9, 2344–2353.
-
(2010)
Mol. Cancer Ther
, vol.9
, pp. 2344-2353
-
-
Parry, D.1
Guzi, T.2
Shanahan, F.3
Davis, N.4
Prabhavalkar, D.5
Wiswell, D.6
Seghezzi, W.7
Paruch, K.8
Dwyer, M.P.9
Doll, R.10
-
51
-
-
77954611291
-
Phase I and pharmacologic study of SNS-032, a potent and selective Cdk2, 7, and 9 inhibitor, in patients with advanced chronic lymphocytic leukemia and multiple myeloma
-
Tong, W.; Chen, R.; Plunkett, W.; Siegel, D.; Sinha, R.; Harvey, R.; Badros, A.; Popplewell, L.; Coutre, S.; Fox, J. Phase I and pharmacologic study of SNS-032, a potent and selective Cdk2, 7, and 9 inhibitor, in patients with advanced chronic lymphocytic leukemia and multiple myeloma. J. Clin. Oncol. 2010, 28, 3015–3022.
-
(2010)
J. Clin. Oncol
, vol.28
, pp. 3015-3022
-
-
Tong, W.1
Chen, R.2
Plunkett, W.3
Siegel, D.4
Sinha, R.5
Harvey, R.6
Badros, A.7
Popplewell, L.8
Coutre, S.9
Fox, J.10
-
52
-
-
68149162135
-
SNS-032 is a potent and selective CDK 2, 7 and 9 inhibitor that drives target modulation in patient samples. Cancer Chemother
-
Conroy, A.; Stockett, D.; Walker, D.; Arkin, M.; Hoch, U.; Fox, J.; Hawtin, R. SNS-032 is a potent and selective CDK 2, 7 and 9 inhibitor that drives target modulation in patient samples. Cancer Chemother. Pharmacol. 2009, 64, 723–732.
-
(2009)
Pharmacol
, vol.64
, pp. 723-732
-
-
Conroy, A.1
Stockett, D.2
Walker, D.3
Arkin, M.4
Hoch, U.5
Fox, J.6
Hawtin, R.7
-
53
-
-
70349180350
-
Validated bioanalytical method for the quantification of RGB-286638, a novel multi-targeted protein kinase inhibitor, in human plasma and urine by liquid chromatography/tandem triple-quadrupole mass spectrometry
-
De Bruijn, P.; Moghaddam-Helmantel, I.; de Jonge, M.; Meyer, T.; Lam, M.; Verweij, J.; Wiemer, E.; Loos, W. Validated bioanalytical method for the quantification of RGB-286638, a novel multi-targeted protein kinase inhibitor, in human plasma and urine by liquid chromatography/tandem triple-quadrupole mass spectrometry. J. Pharm. Biomed. Anal. 2009, 50, 977–982.
-
(2009)
J. Pharm. Biomed. Anal
, vol.50
, pp. 977-982
-
-
De Bruijn, P.1
Moghaddam-Helmantel, I.2
De Jonge, M.3
Meyer, T.4
Lam, M.5
Verweij, J.6
Wiemer, E.7
Loos, W.8
-
54
-
-
84907916584
-
Phase I study of RGB-286638, a novel, multitargeted cyclin-dependent kinase inhibitor in patients with solid tumors. Clin
-
Van der Biessen, D.A.; Burger, H.; de Bruijn, P.; Lamers, C.H.; Naus, N.; Loferer, H.; Wiemer, E.A.; Mathijssen, R.H.; de Jonge, M.J. Phase I study of RGB-286638, a novel, multitargeted cyclin-dependent kinase inhibitor in patients with solid tumors. Clin. Cancer Res. 2014, 20, 4776–4783.
-
(2014)
Cancer Res
, vol.20
, pp. 4776-4783
-
-
Van Der Biessen, D.A.1
Burger, H.2
De Bruijn, P.3
Lamers, C.H.4
Naus, N.5
Loferer, H.6
Wiemer, E.A.7
Mathijssen, R.H.8
De Jonge, M.J.9
-
55
-
-
79960845714
-
Pharmacologic profile of the oral novel pan-CDK inhibitor BAY 1000394 in chemosensitive and chemorefractory tumor models
-
Siemeister, G.; Lucking, U.; Wengner, A.; Lienau, P.; Schatz, C.; Mumberg, D.; Ziegelbauer, K. Pharmacologic profile of the oral novel pan-CDK inhibitor BAY 1000394 in chemosensitive and chemorefractory tumor models. Cancer Res. 2010, 70, 3883–3883.
-
(2010)
Cancer Res
, vol.70
-
-
Siemeister, G.1
Lucking, U.2
Wengner, A.3
Lienau, P.4
Schatz, C.5
Mumberg, D.6
Ziegelbauer, K.7
-
56
-
-
84867422165
-
1000394, a novel cyclin-dependent kinase inhibitor, with potent antitumor activity in mono-and in combination treatment upon oral application
-
Siemeister, G.; Lücking, U.; Wengner, A.; Lienau, P.; Steinke, W.; Schatz, C.; Mumberg, D.; Ziegelbauer, K. BAY 1000394, a novel cyclin-dependent kinase inhibitor, with potent antitumor activity in mono-and in combination treatment upon oral application. Mol. Cancer Ther. 2012, 11, 2265–2273.
-
(2012)
Mol. Cancer Ther
, vol.11
, pp. 2265-2273
-
-
Siemeister, G.1
Lücking, U.2
Wengner, A.3
Lienau, P.4
Steinke, W.5
Schatz, C.6
Mumberg, D.7
Ziegelbauer, K.8
-
57
-
-
84872311254
-
Structure-based design of nitrogen-linked macrocyclic kinase inhibitors leading to the clinical candidate SB1317/TG02, a potent inhibitor of cyclin dependant kinases (CDKs), Janus kinase 2 (JAK2), and Fms-like tyrosine kinase-3 (FLT3)
-
Poulsen, A.; William, A.; Blanchard, S.; Nagaraj, H.; Williams, M.; Wang, H.; Lee, A.; Sun, E.; Teo, E.-L.; Tan, E. Structure-based design of nitrogen-linked macrocyclic kinase inhibitors leading to the clinical candidate SB1317/TG02, a potent inhibitor of cyclin dependant kinases (CDKs), Janus kinase 2 (JAK2), and Fms-like tyrosine kinase-3 (FLT3). J. Mol. Model. 2013, 19, 119–130.
-
(2013)
J. Mol. Model
, vol.19
, pp. 119-130
-
-
Poulsen, A.1
William, A.2
Blanchard, S.3
Nagaraj, H.4
Williams, M.5
Wang, H.6
Lee, A.7
Sun, E.8
Teo, E.-L.9
Tan, E.10
-
58
-
-
0027083108
-
Activation of human cyclin-dependent kinases in vitro
-
Desai, D.; Gu, Y.; Morgan, D.O. Activation of human cyclin-dependent kinases in vitro. Mol. Biol. Cell 1992, 3, 571–582.
-
(1992)
Mol. Biol. Cell
, vol.3
, pp. 571-582
-
-
Desai, D.1
Gu, Y.2
Morgan, D.O.3
-
59
-
-
0027532449
-
Phosphorylation independent activation of human cyclin-dependent kinase 2 by cyclin A in vitro
-
Connell-Crowley, L.; Solomon, M.J.; Wei, N.; Harper, J.W. Phosphorylation independent activation of human cyclin-dependent kinase 2 by cyclin A in vitro. Mol. Biol. Cell 1993, 4, 79–92.
-
(1993)
Mol. Biol. Cell
, vol.4
, pp. 79-92
-
-
Connell-Crowley, L.1
Solomon, M.J.2
Wei, N.3
Harper, J.W.4
-
60
-
-
0026070261
-
Phosphorylation at Thr167 is required for Schizosaccharomyces pombe p34cdc2 function
-
Gould, K.L.; Moreno, S.; Owen, D.J.; Sazer, S.; Nurse, P. Phosphorylation at Thr167 is required for Schizosaccharomyces pombe p34cdc2 function. EMBO J. 1991, 10, 3297–3309.
-
(1991)
EMBO J
, vol.10
, pp. 3297-3309
-
-
Gould, K.L.1
Moreno, S.2
Owen, D.J.3
Sazer, S.4
Nurse, P.5
-
61
-
-
17144415209
-
Design of a novel class of peptide inhibitors of cyclin-dependent kinase/cyclin activation
-
Gondeau, C.; Gerbal-Chaloin, S.; Bello, P.; Aldrian-Herrada, G.; Morris, M.C.; Divita, G. Design of a novel class of peptide inhibitors of cyclin-dependent kinase/cyclin activation. J. Biol. Chem. 2005, 280, 13793–13800.
-
(2005)
J. Biol. Chem
, vol.280
, pp. 13793-13800
-
-
Gondeau, C.1
Gerbal-Chaloin, S.2
Bello, P.3
Aldrian-Herrada, G.4
Morris, M.C.5
Divita, G.6
-
62
-
-
0026847260
-
Cell cycle regulation of vertebrate p34cdc2 activity: Identification of Thr161 as an essential in vivo phosphorylation site
-
Krek, W.; Nigg, E.A. Cell cycle regulation of vertebrate p34cdc2 activity: Identification of Thr161 as an essential in vivo phosphorylation site. New Biol. 1992, 4, 323–329.
-
(1992)
New Biol
, vol.4
, pp. 323-329
-
-
Krek, W.1
Nigg, E.A.2
-
63
-
-
0026713875
-
Cell cycle regulation of CDK2 activity by phosphorylation of Thr160 and Tyr15
-
Gu, Y.; Rosenblatt, J.; Morgan, D.O. Cell cycle regulation of CDK2 activity by phosphorylation of Thr160 and Tyr15. EMBO J. 1992, 11, 3995–4005.
-
(1992)
EMBO J
, vol.11
, pp. 3995-4005
-
-
Gu, Y.1
Rosenblatt, J.2
Morgan, D.O.3
-
64
-
-
0027587321
-
Activation of the various cyclin/cdc2 protein kinases
-
Solomon, M.J. Activation of the various cyclin/cdc2 protein kinases. Curr. Opin. Cell Biol. 1993, 5, 180–186.
-
(1993)
Curr. Opin. Cell Biol
, vol.5
, pp. 180-186
-
-
Solomon, M.J.1
-
65
-
-
0025936623
-
Cdc2 phosphorylation is required for its interaction with cyclin
-
Ducommun, B.; Brambilla, P.; Felix, M.A.; Franza, B.R., Jr.; Karsenti, E.; Draetta, G. cdc2 phosphorylation is required for its interaction with cyclin. EMBO J. 1991, 10, 3311–3319.
-
(1991)
EMBO J
, vol.10
, pp. 3311-3319
-
-
Ducommun, B.1
Brambilla, P.2
Felix, M.A.3
Franza, B.R.4
Karsenti, E.5
Draetta, G.6
-
66
-
-
0027182223
-
Crystal structure of cyclin-dependent kinase 2
-
De Bondt, H.L.; Rosenblatt, J.; Jancarik, J.; Jones, H.D.; Morgan, D.O.; Kim, S.H. Crystal structure of cyclin-dependent kinase 2. Nature 1993, 363, 595–602.
-
(1993)
Nature
, vol.363
, pp. 595-602
-
-
De Bondt, H.L.1
Rosenblatt, J.2
Jancarik, J.3
Jones, H.D.4
Morgan, D.O.5
Kim, S.H.6
-
67
-
-
0028568989
-
Domain movements in protein kinases
-
Cox, S.; Radzio-Andzelm, E.; Taylor, S.S. Domain movements in protein kinases. Curr. Opin. Struct. Biol. 1994, 4, 893–901.
-
(1994)
Curr. Opin. Struct. Biol
, vol.4
, pp. 893-901
-
-
Cox, S.1
Radzio-Andzelm, E.2
Taylor, S.S.3
-
68
-
-
0033224309
-
The structural basis for specificity of substrate and recruitment peptides for cyclin-dependent kinases
-
Brown, N.R.; Noble, M.E.; Endicott, J.A.; Johnson, L.N. The structural basis for specificity of substrate and recruitment peptides for cyclin-dependent kinases. Nat. Cell Biol. 1999, 1, 438–443.
-
(1999)
Nat. Cell Biol
, vol.1
, pp. 438-443
-
-
Brown, N.R.1
Noble, M.E.2
Endicott, J.A.3
Johnson, L.N.4
-
69
-
-
0033605643
-
Effects of phosphorylation of threonine 160 on cyclin-dependent kinase 2 structure and activity
-
Brown, N.R.; Noble, M.E.; Lawrie, A.M.; Morris, M.C.; Tunnah, P.; Divita, G.; Johnson, L.N.; Endicott, J.A. Effects of phosphorylation of threonine 160 on cyclin-dependent kinase 2 structure and activity. J. Biol. Chem. 1999, 274, 8746–8756.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 8746-8756
-
-
Brown, N.R.1
Noble, M.E.2
Lawrie, A.M.3
Morris, M.C.4
Tunnah, P.5
Divita, G.6
Johnson, L.N.7
Endicott, J.A.8
-
70
-
-
4444353636
-
Regulation of protein kinases: Controlling activity through activation segment conformation
-
Nolen, B.; Taylor, S.; Ghosh, G. Regulation of protein kinases: Controlling activity through activation segment conformation. Mol. Cell 2004, 15, 661–675.
-
(2004)
Mol. Cell
, vol.15
, pp. 661-675
-
-
Nolen, B.1
Taylor, S.2
Ghosh, G.3
-
71
-
-
0035724495
-
The role of Thr160 phosphorylation of Cdk2 in substrate recognition
-
Holmes, J.K.; Solomon, M.J. The role of Thr160 phosphorylation of Cdk2 in substrate recognition. Eur. J. Biochem. 2001, 268, 4647–4653.
-
(2001)
Eur. J. Biochem
, vol.268
, pp. 4647-4653
-
-
Holmes, J.K.1
Solomon, M.J.2
-
72
-
-
0034988970
-
Inhibitor binding to active and inactive CDK2: The crystal structure of CDK2-cyclin A/indirubin-5-sulphonate
-
Davies, T.G.; Tunnah, P.; Meijer, L.; Marko, D.; Eisenbrand, G.; Endicott, J.A.; Noble, M.E. Inhibitor binding to active and inactive CDK2: The crystal structure of CDK2-cyclin A/indirubin-5-sulphonate. Structure 2001, 9, 389–397.
-
(2001)
Structure
, vol.9
, pp. 389-397
-
-
Davies, T.G.1
Tunnah, P.2
Meijer, L.3
Marko, D.4
Eisenbrand, G.5
Endicott, J.A.6
Noble, M.E.7
-
73
-
-
17144420076
-
Molecular motions of human cyclin-dependent kinase 2
-
Barrett, C.P.; Noble, M.E. Molecular motions of human cyclin-dependent kinase 2. J. Biol. Chem. 2005, 280, 13993–14005.
-
(2005)
J. Biol. Chem
, vol.280
, pp. 13993-14005
-
-
Barrett, C.P.1
Noble, M.E.2
-
74
-
-
0036710767
-
Pharmacological inhibitors of cyclin-dependent kinases
-
Knockaert, M.; Greengard, P.; Meijer, L. Pharmacological inhibitors of cyclin-dependent kinases. Trends Pharmacol. Sci. 2002, 23, 417–425.
-
(2002)
Trends Pharmacol. Sci
, vol.23
, pp. 417-425
-
-
Knockaert, M.1
Greengard, P.2
Meijer, L.3
-
75
-
-
0037479908
-
Computational model of binding thermodynamics: The design of cyclin-dependent kinase 2 inhibitors
-
Sims, P.A.; Wong, C.F.; McCammon, J.A. A computational model of binding thermodynamics: The design of cyclin-dependent kinase 2 inhibitors. J. Med. Chem. 2003, 46, 3314–3325.
-
(2003)
J. Med. Chem
, vol.46
, pp. 3314-3325
-
-
Sims, P.A.1
Wong, C.F.2
McCammon, J.3
-
76
-
-
77950473958
-
Kinase selectivity potential for inhibitors targeting the ATP binding site
-
Huang, D.; Zhou, T.; Lafleur, K.; Nevado, C.; Caflisch, A. Kinase selectivity potential for inhibitors targeting the ATP binding site: A network analysis. Bioinformatics 2010, 26, 198–204.
-
(2010)
A Network Analysis. Bioinformatics
, vol.26
, pp. 198-204
-
-
Huang, D.1
Zhou, T.2
Lafleur, K.3
Nevado, C.4
Caflisch, A.5
-
77
-
-
84880286488
-
Extra precision docking, free energy calculation and molecular dynamics simulation studies of CDK2 inhibitors
-
Tripathi, S.K.; Muttineni, R.; Singh, S.K. Extra precision docking, free energy calculation and molecular dynamics simulation studies of CDK2 inhibitors. J. Theor. Biol. 2013, 334, 87–100.
-
(2013)
J. Theor. Biol
, vol.334
, pp. 87-100
-
-
Tripathi, S.K.1
Muttineni, R.2
Singh, S.K.3
-
78
-
-
0035990909
-
Structural studies with inhibitors of the cell cycle regulatory kinase cyclin-dependent protein kinase 2
-
Johnson, L.N.; de Moliner, E.; Brown, N.R.; Song, H.; Barford, D.; Endicott, J.A.; Noble, M.E. Structural studies with inhibitors of the cell cycle regulatory kinase cyclin-dependent protein kinase 2. Pharmacol. Ther. 2002, 93, 113–124.
-
(2002)
Pharmacol. Ther
, vol.93
, pp. 113-124
-
-
Johnson, L.N.1
De Moliner, E.2
Brown, N.R.3
Song, H.4
Barford, D.5
Endicott, J.A.6
Noble, M.E.7
-
79
-
-
84887212571
-
Identifying tumor cell growth inhibitors by combinatorial chemistry and zebrafish assays
-
Xiang, J.; Yang, H.; Che, C.; Zou, H.; Wei, Y.; Quan, J.; Zhang, H.; Yang, Z.; Lin, S. Identifying tumor cell growth inhibitors by combinatorial chemistry and zebrafish assays. PLoS ONE 2009, 4, e4361.
-
(2009)
Plos ONE
, vol.4
-
-
Xiang, J.1
Yang, H.2
Che, C.3
Zou, H.4
Wei, Y.5
Quan, J.6
Zhang, H.7
Yang, Z.8
Lin, S.9
-
80
-
-
84881095634
-
An in silico exploration of the interaction mechanism of pyrazolo[1,5-a]pyrimidine type CDK2 inhibitors
-
Li, Y.; Gao, W.; Li, F.; Wang, J.; Zhang, J.; Yang, Y.; Zhang, S.; Yang, L. An in silico exploration of the interaction mechanism of pyrazolo[1,5-a]pyrimidine type CDK2 inhibitors. Mol. Biosyst. 2013, 9, 2266–2281.
-
(2013)
Mol. Biosyst
, vol.9
, pp. 2266-2281
-
-
Li, Y.1
Gao, W.2
Li, F.3
Wang, J.4
Zhang, J.5
Yang, Y.6
Zhang, S.7
Yang, L.8
-
81
-
-
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, et al. 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
-
82
-
-
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, et al. 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
-
83
-
-
84865057198
-
Fascaplysin as a specific inhibitor for CDK4: Insights from molecular modelling
-
Shafiq, M.I.; Steinbrecher, T.; Schmid, R. Fascaplysin as a specific inhibitor for CDK4: Insights from molecular modelling. PLoS ONE 2012, 7, e42612.
-
(2012)
Plos ONE
, vol.7
-
-
Shafiq, M.I.1
Steinbrecher, T.2
Schmid, R.3
-
85
-
-
84905699926
-
Palbociclib: An evidence-based review of its potential in the treatment of breast cancer
-
Cadoo, K.A.; Gucalp, A.; Traina, T.A. Palbociclib: An evidence-based review of its potential in the treatment of breast cancer. Breast Cancer 2014, 6, 123–133.
-
(2014)
Breast Cancer
, vol.6
, pp. 123-133
-
-
Cadoo, K.A.1
Gucalp, A.2
Traina, T.A.3
-
86
-
-
84899888709
-
Retinoblastoma tumor suppressor pathway in breast cancer
-
Witkiewicz, A.K.; Knudsen, E.S. Retinoblastoma tumor suppressor pathway in breast cancer: Prognosis, precision medicine, and therapeutic interventions. Breast Cancer Res. 2014, 16, 207. doi:10.1186/bcr3652.
-
(2014)
Prognosis, Precision Medicine, and Therapeutic Interventions. Breast Cancer Res
, vol.16
, pp. 207
-
-
Witkiewicz, A.K.1
Knudsen, E.S.2
-
87
-
-
1942509495
-
Structural determinants of CDK4 inhibition and design of selective ATP competitive inhibitors
-
McInnes, C.; Wang, S.; Anderson, S.; O’Boyle, J.; Jackson, W.; Kontopidis, G.; Meades, C.; Mezna, M.; Thomas, M.; Wood, G. Structural determinants of CDK4 inhibition and design of selective ATP competitive inhibitors. Chem. Biol. 2004, 11, 525–534.
-
(2004)
Chem. Biol
, vol.11
, pp. 525-534
-
-
McInnes, C.1
Wang, S.2
Anderson, S.3
O’Boyle, J.4
Jackson, W.5
Kontopidis, G.6
Meades, C.7
Mezna, M.8
Thomas, M.9
Wood, G.10
-
88
-
-
33745676300
-
Toward understanding the structural basis of cyclin-dependent kinase 6 specific inhibition
-
Lu, H.; Schulze-Gahmen, U. Toward understanding the structural basis of cyclin-dependent kinase 6 specific inhibition. J. Med. Chem. 2006, 49, 3826–3831.
-
(2006)
J. Med. Chem
, vol.49
, pp. 3826-3831
-
-
Lu, H.1
Schulze-Gahmen, U.2
-
89
-
-
58949085676
-
A novel binding pocket of cyclin-dependent kinase 2
-
Chen, H.; van Duyne, R.; Zhang, N.; Kashanchi, F.; Zeng, C. A novel binding pocket of cyclin-dependent kinase 2. Proteins 2009, 74, 122–132.
-
(2009)
Proteins
, vol.74
, pp. 122-132
-
-
Chen, H.1
Van Duyne, R.2
Zhang, N.3
Kashanchi, F.4
Zeng, C.5
-
90
-
-
29144523190
-
Peptide inhibitors of protein kinases-discovery, characterisation and use
-
Bogoyevitch, M.A.; Barr, R.K.; Ketterman, A.J. Peptide inhibitors of protein kinases-discovery, characterisation and use. Biochim. Biophys. Acta 2005, 1754, 79–99.
-
(2005)
Biochim. Biophys. Acta
, vol.1754
, pp. 79-99
-
-
Bogoyevitch, M.A.1
Barr, R.K.2
Ketterman, A.J.3
-
91
-
-
14844307019
-
The structure of cyclin E1/CDK2: Implications for CDK2 activation and CDK2-independent roles
-
Honda, R.; Lowe, E.D.; Dubinina, E.; Skamnaki, V.; Cook, A.; Brown, N.R.; Johnson, L.N. The structure of cyclin E1/CDK2: Implications for CDK2 activation and CDK2-independent roles. EMBO J. 2005, 24, 452–463.
-
(2005)
EMBO J
, vol.24
, pp. 452-463
-
-
Honda, R.1
Lowe, E.D.2
Dubinina, E.3
Skamnaki, V.4
Cook, A.5
Brown, N.R.6
Johnson, L.N.7
-
92
-
-
34547697834
-
Cyclin B and cyclin A confer different substrate recognition properties on CDK2
-
Brown, N.R.; Lowe, E.D.; Petri, E.; Skamnaki, V.; Antrobus, R.; Johnson, L.N. Cyclin B and cyclin A confer different substrate recognition properties on CDK2. Cell Cycle 2007, 6, 1350–1359.
-
(2007)
Cell Cycle
, vol.6
, pp. 1350-1359
-
-
Brown, N.R.1
Lowe, E.D.2
Petri, E.3
Skamnaki, V.4
Antrobus, R.5
Johnson, L.N.6
-
93
-
-
0030598865
-
The Cdk-activating kinase (CAK) from budding yeast
-
Kaldis, P.; Sutton, A.; Solomon, M.J. The Cdk-activating kinase (CAK) from budding yeast. Cell 1996, 86, 553–564.
-
(1996)
Cell
, vol.86
, pp. 553-564
-
-
Kaldis, P.1
Sutton, A.2
Solomon, M.J.3
-
94
-
-
79957497448
-
Discovery of a potential allosteric ligand binding site in CDK2. ACS
-
Betzi, S.; Alam, R.; Martin, M.; Lubbers, D.J.; Han, H.; Jakkaraj, S.R.; Georg, G.I.; Schonbrunn, E. Discovery of a potential allosteric ligand binding site in CDK2. ACS Chem. Biol. 2011, 6, 492–501.
-
(2011)
Chem. Biol
, vol.6
, pp. 492-501
-
-
Betzi, S.1
Alam, R.2
Martin, M.3
Lubbers, D.J.4
Han, H.5
Jakkaraj, S.R.6
Georg, G.I.7
Schonbrunn, E.8
-
95
-
-
84866449140
-
A novel approach to the discovery of small-molecule ligands of CDK2
-
Martin, M.P.; Alam, R.; Betzi, S.; Ingles, D.J.; Zhu, J.Y.; Schonbrunn, E. A novel approach to the discovery of small-molecule ligands of CDK2. Chembiochem 2012, 13, 2128–2136.
-
(2012)
Chembiochem
, vol.13
, pp. 2128-2136
-
-
Martin, M.P.1
Alam, R.2
Betzi, S.3
Ingles, D.J.4
Zhu, J.Y.5
Schonbrunn, E.6
-
96
-
-
84904488820
-
Structure-based discovery of the first allosteric inhibitors of cyclin-dependent kinase 2
-
Rastelli, G.; Anighoro, A.; Chripkova, M.; Carrassa, L.; Broggini, M. Structure-based discovery of the first allosteric inhibitors of cyclin-dependent kinase 2. Cell Cycle 2014, 13, 2296–2305.
-
(2014)
Cell Cycle
, vol.13
, pp. 2296-2305
-
-
Rastelli, G.1
Anighoro, A.2
Chripkova, M.3
Carrassa, L.4
Broggini, M.5
-
97
-
-
0033163714
-
Four-dimensional control of the cell cycle
-
Pines, J. Four-dimensional control of the cell cycle. Nat. Cell Biol. 1999, 1, E73–E79.
-
(1999)
Nat. Cell Biol
, vol.1
, pp. E73-E79
-
-
Pines, J.1
-
98
-
-
0029767016
-
Structural basis of cyclin-dependent kinase activation by phosphorylation
-
Russo, A.A.; Jeffrey, P.D.; Pavletich, N.P. Structural basis of cyclin-dependent kinase activation by phosphorylation. Nat. Struct. Biol. 1996, 3, 696–700.
-
(1996)
Nat. Struct. Biol
, vol.3
, pp. 696-700
-
-
Russo, A.A.1
Jeffrey, P.D.2
Pavletich, N.P.3
-
99
-
-
0026342401
-
Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase
-
Knighton, D.R.; Zheng, J.H.; Ten Eyck, L.F.; Ashford, V.A.; Xuong, N.H.; Taylor, S.S.; Sowadski, J.M. Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase. Science 1991, 253, 407–414.
-
(1991)
Science
, vol.253
, pp. 407-414
-
-
Knighton, D.R.1
Zheng, J.H.2
Ten Eyck, L.F.3
Ashford, V.A.4
Xuong, N.H.5
Taylor, S.S.6
Sowadski, J.M.7
-
101
-
-
33749503799
-
Combined depletion of cell cycle and transcriptional cyclin-dependent kinase activities induces apoptosis in cancer cells
-
Cai, D.; Latham, V.M.; Zhang, X.; Shapiro, G.I. Combined depletion of cell cycle and transcriptional cyclin-dependent kinase activities induces apoptosis in cancer cells. Cancer Res. 2006, 66, 9270–9280.
-
(2006)
Cancer Res
, vol.66
, pp. 9270-9280
-
-
Cai, D.1
Latham, V.M.2
Zhang, X.3
Shapiro, G.I.4
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