-
2
-
-
0037365789
-
ATM and related protein kinases: Safeguarding genome integrity
-
Shiloh, Y. (2003) ATM and related protein kinases: safeguarding genome integrity. Nature Reviews Cancer 3, 155-168
-
(2003)
Nature Reviews Cancer
, vol.3
, pp. 155-168
-
-
Shiloh, Y.1
-
3
-
-
0024259655
-
Correlation of DNA adduct levels in human lung with cigarette smoking
-
Phillips, D. H. et al. (1988) Correlation of DNA adduct levels in human lung with cigarette smoking. Nature 336, 790-792
-
(1988)
Nature
, vol.336
, pp. 790-792
-
-
Phillips, D.H.1
-
5
-
-
0035941021
-
ATR and ATRIP: Partners in checkpoint signaling
-
Cortez, D. et al. (2001) ATR and ATRIP: partners in checkpoint signaling. Science 294, 1713-1716
-
(2001)
Science
, vol.294
, pp. 1713-1716
-
-
Cortez, D.1
-
6
-
-
0037567268
-
Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes
-
Zou, L. and Elledge, S. J. (2003) Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes. Science 300, 1542-1548
-
(2003)
Science
, vol.300
, pp. 1542-1548
-
-
Zou, L.1
Elledge, S.J.2
-
7
-
-
34250705797
-
The Rad9-Hus1-Rad1 (9-1-1) clamp activates checkpoint signaling via TopBP1
-
Delacroix, S. et al. (2007) The Rad9-Hus1-Rad1 (9-1-1) clamp activates checkpoint signaling via TopBP1. Genes, Development 21, 1472-1477
-
(2007)
Genes, Development
, vol.21
, pp. 1472-1477
-
-
Delacroix, S.1
-
8
-
-
34948889415
-
The Rad9-Hus1-Rad1 checkpoint clamp regulates interaction of TopBP1 withATR
-
Lee, J., Kumagai, A. and Dunphy, W. G. (2007) The Rad9-Hus1-Rad1 checkpoint clamp regulates interaction of TopBP1 withATR. Journal of Biological Chemistry 282, 28036-28044
-
(2007)
Journal of Biological Chemistry
, vol.282
, pp. 28036-28044
-
-
Lee, J.1
Kumagai, A.2
Dunphy, W.G.3
-
9
-
-
44849093460
-
TopBP1 activates ATR through ATRIP and a PIKK regulatory domain
-
Mordes, D. A. et al. (2008) TopBP1 activates ATR through ATRIP and a PIKK regulatory domain. Genes, Development 22, 1478-1489
-
(2008)
Genes, Development
, vol.22
, pp. 1478-1489
-
-
Mordes, D.A.1
-
10
-
-
0035955398
-
Recruitment of Mec1 and Ddc1 checkpoint proteins to double-strand breaks through distinct mechanisms
-
Kondo, T. et al. (2001) Recruitment of Mec1 and Ddc1 checkpoint proteins to double-strand breaks through distinct mechanisms. Science 294, 867-870
-
(2001)
Science
, vol.294
, pp. 867-870
-
-
Kondo, T.1
-
11
-
-
0035498938
-
Two checkpoint complexes are independently recruited to sites of DNA damage in vivo
-
Melo, J. A., Cohen, J. and Toczyski, D. P. (2001) Two checkpoint complexes are independently recruited to sites of DNA damage in vivo. Genes, Development 15, 2809-2821
-
(2001)
Genes, Development
, vol.15
, pp. 2809-2821
-
-
Melo, J.A.1
Cohen, J.2
Toczyski, D.P.3
-
12
-
-
34249947699
-
ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage
-
Matsuoka, S. et al. (2007) ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage. Science 316, 1160-1166
-
(2007)
Science
, vol.316
, pp. 1160-1166
-
-
Matsuoka, S.1
-
13
-
-
0033555260
-
A role for ATR in the DNA damage-induced phosphorylation of p53
-
Tibbetts, R. S. et al. (1999) A role for ATR in the DNA damage-induced phosphorylation of p53. Genes, Development 13, 152-157
-
(1999)
Genes, Development
, vol.13
, pp. 152-157
-
-
Tibbetts, R.S.1
-
14
-
-
0033572746
-
Serine15 phosphorylation stimulates p53 transactivation but does not directly influence interaction with HDM2
-
Dumaz, N. and Meek, D. W. (1999) Serine15 phosphorylation stimulates p53 transactivation but does not directly influence interaction with HDM2. EMBO Journal 18, 7002-7010
-
(1999)
EMBO Journal
, vol.18
, pp. 7002-7010
-
-
Dumaz, N.1
Meek, D.W.2
-
16
-
-
84887087577
-
TargetingATR inDNAdamage response and cancer therapeutics
-
Fokas, E. et al. (2013) TargetingATR inDNAdamage response and cancer therapeutics. Cancer Treatment Reviews 40, 109-117
-
(2013)
Cancer Treatment Reviews
, vol.40
, pp. 109-117
-
-
Fokas, E.1
-
17
-
-
0035979213
-
ATR inhibition selectively sensitizes G1 checkpoint-deficient cells to lethal premature chromatin condensation
-
Nghiem, P. et al. (2001) ATR inhibition selectively sensitizes G1 checkpoint-deficient cells to lethal premature chromatin condensation. Proceedings of the National Academy of Sciences USA 98, 9092-9097
-
(2001)
Proceedings of the National Academy of Sciences USA
, vol.98
, pp. 9092-9097
-
-
Nghiem, P.1
-
18
-
-
74549189337
-
New insights into checkpoint kinase 1 in the DNA damage response signaling network
-
Dai, Y. and Grant, S. (2010) New insights into checkpoint kinase 1 in the DNA damage response signaling network. Clinical Cancer Research 16, 376-383
-
(2010)
Clinical Cancer Research
, vol.16
, pp. 376-383
-
-
Dai, Y.1
Grant, S.2
-
20
-
-
78449259637
-
CHK1 inhibition as a strategy for targeting fanconi anemia (FA) DNA repair pathway deficient tumors
-
Chen, C. et al. (2009) CHK1 inhibition as a strategy for targeting fanconi anemia (FA) DNA repair pathway deficient tumors. Molecular Cancer 8, 1-16
-
(2009)
Molecular Cancer
, vol.8
, pp. 1-16
-
-
Chen, C.1
-
21
-
-
81255143440
-
Therapeutic implications for the induced levels of CHK1 in MYC-expressing cancer cells
-
Höglund, A. et al. (2011) Therapeutic implications for the induced levels of CHK1 in MYC-expressing cancer cells. Clinical Cancer Research 17, 7067-7079
-
(2011)
Clinical Cancer Research
, vol.17
, pp. 7067-7079
-
-
Höglund, A.1
-
22
-
-
79952775174
-
RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma
-
Cole, K. A. et al. (2011) RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma. Proceedings of the National Academy of Sciences USA 108, 3336-3341
-
(2011)
Proceedings of the National Academy of Sciences USA
, vol.108
, pp. 3336-3341
-
-
Cole, K.A.1
-
23
-
-
84855418471
-
Oncogenic stress sensitizes murine cancers to hypomorphic suppression of ATR
-
Schoppy, D. W. et al. (2012) Oncogenic stress sensitizes murine cancers to hypomorphic suppression of ATR. The Journal of Clinical Investigation 122, 241-252
-
(2012)
The Journal of Clinical Investigation
, vol.122
, pp. 241-252
-
-
Schoppy, D.W.1
-
24
-
-
85006807600
-
-
http://clinicaltrials. gov/ct2/show/NCT01955668
-
-
-
-
25
-
-
85006828683
-
-
https://www. clinicaltrialsregister. eu/ctr-search/trial/2012-003126-25/GB
-
-
-
-
26
-
-
0028170210
-
A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002
-
Vlahos, C. J. et al. (1994) A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002). Journal of Biological Chemistry 269, 5241-5248
-
(1994)
Journal of Biological Chemistry
, vol.269
, pp. 5241-5248
-
-
Vlahos, C.J.1
-
27
-
-
0030814125
-
Radiosensitization of human tumor cells by the phosphatidylinositol3-kinase inhibitors wortmannin and LY294002 correlates with inhibition of DNA-dependent protein kinase and prolonged G2-M delay
-
Rosenzweig, K. E. et al. (1997) Radiosensitization of human tumor cells by the phosphatidylinositol3-kinase inhibitors wortmannin and LY294002 correlates with inhibition of DNA-dependent protein kinase and prolonged G2-M delay. Clinical Cancer Research 3, 1149-1156
-
(1997)
Clinical Cancer Research
, vol.3
, pp. 1149-1156
-
-
Rosenzweig, K.E.1
-
28
-
-
31544444486
-
Phosphatidylinositol 3-kinase inhibition by LY294002 radiosensitizes human cervical cancer cell lines
-
Lee, C. M. et al. (2006) Phosphatidylinositol 3-kinase inhibition by LY294002 radiosensitizes human cervical cancer cell lines. Clinical Cancer Research 12, 250-256
-
(2006)
Clinical Cancer Research
, vol.12
, pp. 250-256
-
-
Lee, C.M.1
-
29
-
-
33646383684
-
A pharmacological map of the PI3-K family defines a role for p110 in insulin signaling
-
Knight, Z. A. et al. (2006) A pharmacological map of the PI3-K family defines a role for p110 in insulin signaling. Cell 125, 733-747
-
(2006)
Cell
, vol.125
, pp. 733-747
-
-
Knight, Z.A.1
-
30
-
-
0032189483
-
Inhibition of phosphoinositide 3-kinase related kinases by the radiosensitizing agent wortmannin
-
Sarkaria, J. N. et al. (1998) Inhibition of phosphoinositide 3-kinase related kinases by the radiosensitizing agent wortmannin. Cancer Research 58, 4375-4382
-
(1998)
Cancer Research
, vol.58
, pp. 4375-4382
-
-
Sarkaria, J.N.1
-
31
-
-
0033199892
-
Inhibition of ATM and ATR kinase activities by the radiosensitizing agent
-
Sarkaria, J. N. et al. (1999) Inhibition of ATM and ATR kinase activities by the radiosensitizing agent, Caffeine. Cancer Research 59, 4375-4382
-
(1999)
Caffeine. Cancer Research
, vol.59
, pp. 4375-4382
-
-
Sarkaria, J.N.1
-
32
-
-
85006825555
-
-
University of Rochester, USA; University of Utah
-
Planelles, V., Roshal, M. and Zhu, Y. H. (2003) Patent WO2003068929A2, University of Rochester, USA; University of Utah
-
(2003)
-
-
Planelles, V.1
Roshal, M.2
Zhu, Y.H.3
-
35
-
-
73149106613
-
Inhibition ofATRprotein kinase activity by schisandrin B in DNA damage response
-
Nishida, H. et al. (2009) Inhibition ofATRprotein kinase activity by schisandrin B in DNA damage response. Nucleic Acids Research 37, 5678-5689
-
(2009)
Nucleic Acids Research
, vol.37
, pp. 5678-5689
-
-
Nishida, H.1
-
36
-
-
84876950862
-
Characterization of Torin2, an ATP-competitive inhibitor of mTOR, ATM, andATR
-
Liu, Q. et al. (2013) Characterization of Torin2, an ATP-competitive inhibitor of mTOR, ATM, andATR. Cancer Research 73, 2574-2586
-
(2013)
Cancer Research
, vol.73
, pp. 2574-2586
-
-
Liu, Q.1
-
37
-
-
79958865837
-
Acell-based screen identifies ATR inhibitors with synthetic lethal properties for cancer-associated mutations
-
Toledo, L. I. et al. (2011)Acell-based screen identifies ATR inhibitors with synthetic lethal properties for cancer-associated mutations. Nature Structural, Molecular Biology 18, 721-727
-
(2011)
Nature Structural, Molecular Biology
, vol.18
, pp. 721-727
-
-
Toledo, L.I.1
-
38
-
-
33644757806
-
TopBP1 activates the ATR-ATRIP complex
-
Kumagai, A. et al. (2006) TopBP1 activates the ATR-ATRIP complex. Cell 124, 943-955
-
(2006)
Cell
, vol.124
, pp. 943-955
-
-
Kumagai, A.1
-
39
-
-
38949124412
-
ATR signaling can drive cells into senescence in the absence ofDNAbreaks
-
Toledo, L. I. et al. (2008) ATR signaling can drive cells into senescence in the absence ofDNAbreaks. Genes, Development 22, 297-302
-
(2008)
Genes, Development
, vol.22
, pp. 297-302
-
-
Toledo, L.I.1
-
40
-
-
85006748594
-
-
http://www. merckmillipore. com/life-scienceresearch/ucn-01/EMD-BIO-539644/p-R66b. s1LTrMAAAEWx2EfVhTm
-
-
-
-
41
-
-
51049109033
-
Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity
-
Maira, S.-M. et al. (2008) Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity. Molecular Cancer Therapeutics 7, 1851-1863
-
(2008)
Molecular Cancer Therapeutics
, vol.7
, pp. 1851-1863
-
-
Maira, S.-M.1
-
42
-
-
85006696738
-
-
http://clinicaltrials. gov/show/NCT00620594
-
-
-
-
43
-
-
70350228529
-
Dual phosphoinositide 3-kinase/mammalian target of rapamycin blockade is an effective radiosensitizing strategy for the treatment of non-small cell lung cancer harboring K-RAS mutations
-
Konstantinidou, G. et al. (2009) Dual phosphoinositide 3-kinase/mammalian target of rapamycin blockade is an effective radiosensitizing strategy for the treatment of non-small cell lung cancer harboring K-RAS mutations. Cancer Research 69, 7644-7652
-
(2009)
Cancer Research
, vol.69
, pp. 7644-7652
-
-
Konstantinidou, G.1
-
44
-
-
78649929369
-
Combining ATR suppression with oncogenic ras synergistically increases genomic instability, causing synthetic lethality or tumorigenesis in a dosage-dependent manner
-
Gilad, O. et al. (2010) Combining ATR suppression with oncogenic ras synergistically increases genomic instability, causing synthetic lethality or tumorigenesis in a dosage-dependent manner. Cancer Research 70, 9693-9702
-
(2010)
Cancer Research
, vol.70
, pp. 9693-9702
-
-
Gilad, O.1
-
45
-
-
79960834396
-
Identification and evaluation of a potent novel ATR inhibitor, NU6027, in breast and ovarian cancer cell lines
-
Peasland, A. et al. (2011) Identification and evaluation of a potent novel ATR inhibitor, NU6027, in breast and ovarian cancer cell lines. British Journal of Cancer 105, 372-381
-
(2011)
British Journal of Cancer
, vol.105
, pp. 372-381
-
-
Peasland, A.1
-
46
-
-
85006750570
-
-
Dana Farber Cancer Institute Inc., USA
-
D'Andrea, A. D. and Taniguchi, T. (2006) Patent WO2006127978A2, Dana Farber Cancer Institute Inc., USA
-
, vol.2006
-
-
D'Andrea, A.D.1
Taniguchi, T.2
-
47
-
-
4043133287
-
ATR couples FANCD2monoubiquitination to the DNA-damage response
-
Andreassen, P. R., D'Andrea, A. D. and Taniguchi, T. (2004)ATR couples FANCD2monoubiquitination to the DNA-damage response. Genes, Development 18, 1958-1963
-
(2004)
Genes, Development
, vol.18
, pp. 1958-1963
-
-
Andreassen, P.R.1
D'Andrea, A.D.2
Taniguchi, T.3
-
48
-
-
33748656748
-
Phosphorylation of FANCD2 on two novel sites is required for mitomycin C resistance
-
Ho, G. P. H. et al. (2006) Phosphorylation of FANCD2 on two novel sites is required for mitomycin C resistance. Molecular and Cellular Biology 26, 7005-7015
-
(2006)
Molecular and Cellular Biology
, vol.26
, pp. 7005-7015
-
-
Ho, G.P.H.1
-
49
-
-
85006816636
-
-
Cgk Co., Ltd., S. Korea
-
Kim, T. K., Won, J.-J. and Yi, Y.-W. (2007) Patent WO2007015632A1, Cgk Co., Ltd., S. Korea
-
(2007)
-
-
Kim, T.K.1
Won, J.-J.2
Yi, Y.-W.3
-
50
-
-
33745310473
-
Small molecule-based reversible reprogramming of cellular lifespan
-
Won, J. et al. (2006) Small molecule-based reversible reprogramming of cellular lifespan. Nature Chemical Biology 2, 369-374
-
(2006)
Nature Chemical Biology
, vol.2
, pp. 369-374
-
-
Won, J.1
-
51
-
-
45549086894
-
Retraction: Small molecule-based reversible reprogramming of cellular lifespan
-
Won, J. et al. (2008) Retraction: small molecule-based reversible reprogramming of cellular lifespan. Nature Chemical Biology 4, 431-431
-
(2008)
Nature Chemical Biology
, vol.4
, pp. 431
-
-
Won, J.1
-
52
-
-
85006731381
-
-
Astrazeneca AB, Swed. ; Astrazeneca UK Limited
-
Foote, K. M. and Nissink, J. W. M. (2010) Patent WO2010073034A1, Astrazeneca AB, Swed. ; Astrazeneca UK Limited
-
(2010)
-
-
Foote, K.M.1
Nissink, J.W.M.2
-
53
-
-
85006752883
-
-
AstraZeneca AB, Swed. ; AstraZeneca UK Limited
-
Foote, K. M., Nissink, J. W. M. and Turner, P. (2011) Patent WO2011154737A1, AstraZeneca AB, Swed. ; AstraZeneca UK Limited
-
(2011)
-
-
Foote, K.M.1
Nissink, J.W.M.2
Turner, P.3
-
54
-
-
85006731373
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2010) Patent WO2010054398A1, Vertex Pharmaceuticals Incorporated, USA
-
(2010)
-
-
Charrier, J.-D.1
-
55
-
-
85006752873
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) Patent WO2011143426A1, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
56
-
-
85006825598
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2010) Patent WO2010071837A1, Vertex Pharmaceuticals Incorporated, USA
-
(2010)
-
-
Charrier, J.-D.1
-
57
-
-
85006748585
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D., Durrant, S. J. and Knegtel, R. (2013) Patent WO2013071085A1, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Charrier, J.-D.1
Durrant, S.J.2
Knegtel, R.3
-
58
-
-
85006825594
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) Patent WO2011143419A1, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
59
-
-
85006814848
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) Patent WO2011143399A1, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
60
-
-
85006822213
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) Patent WO2011143422A1, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
61
-
-
85006772610
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) PatentWO2011143425A2, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
62
-
-
85006812002
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D., Durrant, S. J. and Shaw, D. M. (2013) Patent WO2013071088A1, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Charrier, J.-D.1
Durrant, S.J.2
Shaw, D.M.3
-
63
-
-
85006815076
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) PatentWO2011143423A2, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
64
-
-
85006807610
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. and Kay, D. (2013) Patent WO2013071094A1, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Charrier, J.-D.1
Kay, D.2
-
65
-
-
85006720681
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2012) PatentWO2012138938A1, Vertex Pharmaceuticals Incorporated, USA
-
(2012)
-
-
Charrier, J.-D.1
-
66
-
-
85006700427
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2011) PatentWO2011163527A1, Vertex Pharmaceuticals Incorporated, USA
-
(2011)
-
-
Charrier, J.-D.1
-
67
-
-
85006791753
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2013) PatentWO2013071090A1, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Charrier, J.-D.1
-
68
-
-
85006791825
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2013) PatentWO2013049726A2, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Charrier, J.-D.1
-
69
-
-
85006736126
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Charrier, J.-D. et al. (2013) PatentWO2013049719A1, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Charrier, J.-D.1
-
70
-
-
85006736123
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Everitt, S. et al. (2012) Patent WO2012178124A1, Vertex Pharmaceuticals Incorporated, USA
-
(2012)
-
-
Everitt, S.1
-
71
-
-
85006736131
-
-
Vertex Pharmaceuticals Incorporated, USA
-
MacCormick, S. etal. (2012)PatentWO2012178123A1, Vertex Pharmaceuticals Incorporated, USA 72
-
(2012)
, vol.72
-
-
MacCormick, S.1
-
72
-
-
85006791821
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Pollard J. R., Reaper P. M. (2013)Patent WO2013049859A1, Vertex Pharmaceuticals Incorporated, USA
-
(2013)
-
-
Pollard, J.R.1
-
73
-
-
85006771467
-
-
Vertex Pharmaceuticals Incorporated, USA
-
Storck, P.-H. et al. (2012) Patent WO2012178125A1, Vertex Pharmaceuticals Incorporated, USA
-
(2012)
-
-
Storck, P.-H.1
-
74
-
-
84875143334
-
Discovery of 4-{4-[(3R)-3-Methylmorpholin-4-yl]-6-[1-(methylsulfonyl) cyclopropyl]pyrimidin-2-yl}-1H-indole (AZ20): A potent and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity
-
Foote, K. M. et al. (2013) Discovery of 4-{4-[(3R)-3-Methylmorpholin-4-yl]-6-[1-(methylsulfonyl) cyclopropyl]pyrimidin-2-yl}-1H-indole (AZ20): a potent and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity. Journal of Medicinal Chemistry 56, 2125-2138
-
(2013)
Journal of Medicinal Chemistry
, vol.56
, pp. 2125-2138
-
-
Foote, K.M.1
-
75
-
-
79959376888
-
Selective killing of ATM-or p53-deficient cancer cells through inhibition of ATR
-
Reaper, P. M. et al. (2011) Selective killing of ATM-or p53-deficient cancer cells through inhibition of ATR. Nature Chemical Biology 7, 428-430
-
(2011)
Nature Chemical Biology
, vol.7
, pp. 428-430
-
-
Reaper, P.M.1
-
76
-
-
79953773734
-
Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents
-
Charrier, J.-D. et al. (2011) Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents. Journal of Medicinal Chemistry 54, 2320-2330
-
(2011)
Journal of Medicinal Chemistry
, vol.54
, pp. 2320-2330
-
-
Charrier, J.-D.1
-
77
-
-
72949105314
-
CYP3A catalyses schizandrin biotransformation in human, minipig and rat liver microsomes
-
Cao, Y. F. et al. (2010) CYP3A catalyses schizandrin biotransformation in human, minipig and rat liver microsomes. Xenobiotica 40, 38-47
-
(2010)
Xenobiotica
, vol.40
, pp. 38-47
-
-
Cao, Y.F.1
-
78
-
-
77649204688
-
Selectively nonselective kinase inhibition: Striking the right balance
-
Morphy, R. (2009) Selectively nonselective kinase inhibition: striking the right balance. Journal of Medicinal Chemistry 53, 1413-1437
-
(2009)
Journal of Medicinal Chemistry
, vol.53
, pp. 1413-1437
-
-
Morphy, R.1
-
79
-
-
75149130051
-
Targeting the cancer kinome through polypharmacology
-
Knight, Z. A., Lin, H. and Shokat, K. M. (2010)Targeting the cancer kinome through polypharmacology. Nature Reviews Cancer 10, 130-137
-
(2010)
Nature Reviews Cancer
, vol.10
, pp. 130-137
-
-
Knight, Z.A.1
Lin, H.2
Shokat, K.M.3
-
80
-
-
84861943484
-
Chemical genetic discovery of targets and anti-targets for cancer polypharmacology
-
Dar, A. C. et al. (2012) Chemical genetic discovery of targets and anti-targets for cancer polypharmacology. Nature 486, 80-84
-
(2012)
Nature
, vol.486
, pp. 80-84
-
-
Dar, A.C.1
-
81
-
-
77954938500
-
Prospects for the use of ATR inhibitors to treat cancer
-
Wagner, J. M. and Kaufmann, S. H. (2010) Prospects for the use of ATR inhibitors to treat cancer. Pharmaceuticals 3, 1311-1334
-
(2010)
Pharmaceuticals
, vol.3
, pp. 1311-1334
-
-
Wagner, J.M.1
Kaufmann, S.H.2
|