-
1
-
-
47749106789
-
Biphenyl amide p38 kinase inhibitors 4: DFG-in and DFG-out binding modes
-
Angell R.M., Angell T.D., Bamborough P., Bamford M.J., Chung C.W., Cockerill S.G., Flack S.S., Jones K.L., Laine D.I., Longstaff T., et al. Biphenyl amide p38 kinase inhibitors 4: DFG-in and DFG-out binding modes. Bioorg. Med. Chem. Lett. 18 (2008) 4433-4437
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 4433-4437
-
-
Angell, R.M.1
Angell, T.D.2
Bamborough, P.3
Bamford, M.J.4
Chung, C.W.5
Cockerill, S.G.6
Flack, S.S.7
Jones, K.L.8
Laine, D.I.9
Longstaff, T.10
-
2
-
-
0032568055
-
Design of allele-specific inhibitors to probe protein kinase signaling
-
Bishop A.C., Shah K., Liu Y., Witucki L., Kung C., and Shokat K.M. Design of allele-specific inhibitors to probe protein kinase signaling. Curr. Biol. 8 (1998) 257-266
-
(1998)
Curr. Biol.
, vol.8
, pp. 257-266
-
-
Bishop, A.C.1
Shah, K.2
Liu, Y.3
Witucki, L.4
Kung, C.5
Shokat, K.M.6
-
3
-
-
0033518610
-
Generation of monospecific nanomolar tyrosine kinase inhibitors via a chemical genetic approach
-
Bishop A.C., Kung C.Y., Shah K., Witucki L., Shokat K.M., and Liu Y. Generation of monospecific nanomolar tyrosine kinase inhibitors via a chemical genetic approach. J. Am. Chem. Soc. 121 (1999) 627-631
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 627-631
-
-
Bishop, A.C.1
Kung, C.Y.2
Shah, K.3
Witucki, L.4
Shokat, K.M.5
Liu, Y.6
-
4
-
-
67649400239
-
Design and use of analog-sensitive protein kinases
-
Ausubel F.M. (Ed), John Wiley & Sons, New York
-
Blethrow J., Zhang C., Shokat K.M., and Weiss E.L. Design and use of analog-sensitive protein kinases. In: Ausubel F.M. (Ed). Current Protocols in Molecular Biology (2004), John Wiley & Sons, New York 1-19
-
(2004)
Current Protocols in Molecular Biology
, pp. 1-19
-
-
Blethrow, J.1
Zhang, C.2
Shokat, K.M.3
Weiss, E.L.4
-
5
-
-
0036635291
-
Glivec (STI571, imatinib), a rationally developed, targeted anticancer drug
-
Capdeville R., Buchdunger E., Zimmermann J., and Matter A. Glivec (STI571, imatinib), a rationally developed, targeted anticancer drug. Nat. Rev. Drug Discov. 1 (2002) 493-502
-
(2002)
Nat. Rev. Drug Discov.
, vol.1
, pp. 493-502
-
-
Capdeville, R.1
Buchdunger, E.2
Zimmermann, J.3
Matter, A.4
-
6
-
-
5444244504
-
Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase
-
Cumming J.G., McKenzie C.L., Bowden S.G., Campbell D., Masters D.J., Breed J., and Jewsbury P.J. Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase. Bioorg. Med. Chem. Lett. 14 (2004) 5389-5394
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 5389-5394
-
-
Cumming, J.G.1
McKenzie, C.L.2
Bowden, S.G.3
Campbell, D.4
Masters, D.J.5
Breed, J.6
Jewsbury, P.J.7
-
7
-
-
15944404601
-
The development of imatinib as a therapeutic agent for chronic myeloid leukemia
-
Deininger M., Buchdunger E., and Druker B.J. The development of imatinib as a therapeutic agent for chronic myeloid leukemia. Blood 105 (2005) 2640-2653
-
(2005)
Blood
, vol.105
, pp. 2640-2653
-
-
Deininger, M.1
Buchdunger, E.2
Druker, B.J.3
-
8
-
-
33748851665
-
Discovery of aminoquinazolines as potent, orally bioavailable inhibitors of Lck: Synthesis, SAR, and in vivo anti-inflammatory activity
-
Dimauro E.F., Newcomb J., Nunes J.J., Bemis J.E., Boucher C., Buchanan J.L., Buckner W.H., Cee V.J., Chai L., Deak H.L., et al. Discovery of aminoquinazolines as potent, orally bioavailable inhibitors of Lck: Synthesis, SAR, and in vivo anti-inflammatory activity. J. Med. Chem. 49 (2006) 5671-5686
-
(2006)
J. Med. Chem.
, vol.49
, pp. 5671-5686
-
-
Dimauro, E.F.1
Newcomb, J.2
Nunes, J.J.3
Bemis, J.E.4
Boucher, C.5
Buchanan, J.L.6
Buckner, W.H.7
Cee, V.J.8
Chai, L.9
Deak, H.L.10
-
10
-
-
19944434344
-
Identification of novel p38alpha MAP kinase inhibitors using fragment-based lead generation
-
Gill A.L., Frederickson M., Cleasby A., Woodhead S.J., Carr M.G., Woodhead A.J., Walker M.T., Congreve M.S., Devine L.A., Tisi D., et al. Identification of novel p38alpha MAP kinase inhibitors using fragment-based lead generation. J. Med. Chem. 48 (2005) 414-426
-
(2005)
J. Med. Chem.
, vol.48
, pp. 414-426
-
-
Gill, A.L.1
Frederickson, M.2
Cleasby, A.3
Woodhead, S.J.4
Carr, M.G.5
Woodhead, A.J.6
Walker, M.T.7
Congreve, M.S.8
Devine, L.A.9
Tisi, D.10
-
11
-
-
0842310394
-
The structural basis for autoinhibition of FLT3 by the juxtamembrane domain
-
Griffith J., Black J., Faerman C., Swenson L., Wynn M., Lu F., Lippke J., and Saxena K. The structural basis for autoinhibition of FLT3 by the juxtamembrane domain. Mol. Cell 13 (2004) 169-178
-
(2004)
Mol. Cell
, vol.13
, pp. 169-178
-
-
Griffith, J.1
Black, J.2
Faerman, C.3
Swenson, L.4
Wynn, M.5
Lu, F.6
Lippke, J.7
Saxena, K.8
-
12
-
-
0030029143
-
Discovery of a novel, potent, and Src family-selective tyrosine kinase inhibitor. Study of Lck- and FynT-dependent T cell activation
-
Hanke J.H., Gardner J.P., Dow R.L., Changelian P.S., Brissette W.H., Weringer E.J., Pollok B.A., and Connelly P.A. Discovery of a novel, potent, and Src family-selective tyrosine kinase inhibitor. Study of Lck- and FynT-dependent T cell activation. J. Biol. Chem. 271 (1996) 695-701
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 695-701
-
-
Hanke, J.H.1
Gardner, J.P.2
Dow, R.L.3
Changelian, P.S.4
Brissette, W.H.5
Weringer, E.J.6
Pollok, B.A.7
Connelly, P.A.8
-
13
-
-
31344438721
-
SAR and inhibitor complex structure determination of a novel class of potent and specific Aurora kinase inhibitors
-
Heron N.M., Anderson M., Blowers D.P., Breed J., Eden J.M., Green S., Hill G.B., Johnson T., Jung F.H., McMiken H.H., et al. SAR and inhibitor complex structure determination of a novel class of potent and specific Aurora kinase inhibitors. Bioorg. Med. Chem. Lett. 16 (2006) 1320-1323
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 1320-1323
-
-
Heron, N.M.1
Anderson, M.2
Blowers, D.P.3
Breed, J.4
Eden, J.M.5
Green, S.6
Hill, G.B.7
Johnson, T.8
Jung, F.H.9
McMiken, H.H.10
-
14
-
-
0028582185
-
Crystal structure of the tyrosine kinase domain of the human insulin receptor
-
Hubbard S.R., Wei L., Ellis L., and Hendrickson W.A. Crystal structure of the tyrosine kinase domain of the human insulin receptor. Nature 372 (1994) 746-754
-
(1994)
Nature
, vol.372
, pp. 746-754
-
-
Hubbard, S.R.1
Wei, L.2
Ellis, L.3
Hendrickson, W.A.4
-
15
-
-
33646755174
-
A Src-like inactive conformation in the abl tyrosine kinase domain
-
10.1371/journal.pbio.0040144 Published online May 2, 2006
-
Levinson N.M., Kuchment O., Shen K., Young M.A., Koldobskiy M., Karplus M., Cole P.A., and Kuriyan J. A Src-like inactive conformation in the abl tyrosine kinase domain. PLoS Biol. 4 (2006) e144 10.1371/journal.pbio.0040144 Published online May 2, 2006
-
(2006)
PLoS Biol.
, vol.4
-
-
Levinson, N.M.1
Kuchment, O.2
Shen, K.3
Young, M.A.4
Koldobskiy, M.5
Karplus, M.6
Cole, P.A.7
Kuriyan, J.8
-
16
-
-
33745298429
-
Rational design of inhibitors that bind to inactive kinase conformations
-
Liu Y., and Gray N.S. Rational design of inhibitors that bind to inactive kinase conformations. Nat. Chem. Biol. 2 (2006) 358-364
-
(2006)
Nat. Chem. Biol.
, vol.2
, pp. 358-364
-
-
Liu, Y.1
Gray, N.S.2
-
17
-
-
0033200390
-
Structural basis for selective inhibition of Src family kinases by PP1
-
Liu Y., Bishop A., Witucki L., Kraybill B., Shimizu E., Tsien J., Ubersax J., Blethrow J., Morgan D.O., and Shokat K.M. Structural basis for selective inhibition of Src family kinases by PP1. Chem. Biol. 6 (1999) 671-678
-
(1999)
Chem. Biol.
, vol.6
, pp. 671-678
-
-
Liu, Y.1
Bishop, A.2
Witucki, L.3
Kraybill, B.4
Shimizu, E.5
Tsien, J.6
Ubersax, J.7
Blethrow, J.8
Morgan, D.O.9
Shokat, K.M.10
-
18
-
-
2942542387
-
Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinase
-
Mol C.D., Dougan D.R., Schneider T.R., Skene R.J., Kraus M.L., Scheibe D.N., Snell G.P., Zou H., Sang B.C., and Wilson K.P. Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinase. J. Biol. Chem. 279 (2004) 31655-31663
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 31655-31663
-
-
Mol, C.D.1
Dougan, D.R.2
Schneider, T.R.3
Skene, R.J.4
Kraus, M.L.5
Scheibe, D.N.6
Snell, G.P.7
Zou, H.8
Sang, B.C.9
Wilson, K.P.10
-
19
-
-
0036682301
-
Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571)
-
Nagar B., Bornmann W.G., Pellicena P., Schindler T., Veach D.R., Miller W.T., Clarkson B., and Kuriyan J. Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571). Cancer Res. 62 (2002) 4236-4243
-
(2002)
Cancer Res.
, vol.62
, pp. 4236-4243
-
-
Nagar, B.1
Bornmann, W.G.2
Pellicena, P.3
Schindler, T.4
Veach, D.R.5
Miller, W.T.6
Clarkson, B.7
Kuriyan, J.8
-
20
-
-
33746258750
-
A general strategy for creating "inactive-conformation" abl inhibitors
-
Okram B., Nagle A., Adrian F.J., Lee C., Ren P., Wang X., Sim T., Xie Y., Wang X., Xia G., et al. A general strategy for creating "inactive-conformation" abl inhibitors. Chem. Biol. 13 (2006) 779-786
-
(2006)
Chem. Biol.
, vol.13
, pp. 779-786
-
-
Okram, B.1
Nagle, A.2
Adrian, F.J.3
Lee, C.4
Ren, P.5
Wang, X.6
Sim, T.7
Xie, Y.8
Wang, X.9
Xia, G.10
-
21
-
-
0344395603
-
Bypassing a kinase activity with an ATP-competitive drug
-
Papa F.R., Zhang C., Shokat K., and Walter P. Bypassing a kinase activity with an ATP-competitive drug. Science 302 (2003) 1533-1537
-
(2003)
Science
, vol.302
, pp. 1533-1537
-
-
Papa, F.R.1
Zhang, C.2
Shokat, K.3
Walter, P.4
-
22
-
-
18344395134
-
Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site
-
Pargellis C., Tong L., Churchill L., Cirillo P.F., Gilmore T., Graham A.G., Grob P.M., Hickey E.R., Moss N., Pav S., and Regan J. Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site. Nat. Struct. Biol. 9 (2002) 268-272
-
(2002)
Nat. Struct. Biol.
, vol.9
, pp. 268-272
-
-
Pargellis, C.1
Tong, L.2
Churchill, L.3
Cirillo, P.F.4
Gilmore, T.5
Graham, A.G.6
Grob, P.M.7
Hickey, E.R.8
Moss, N.9
Pav, S.10
Regan, J.11
-
23
-
-
0036463987
-
Disabling Abl-perspectives on Abl kinase regulation and cancer therapeutics
-
Sawyers C.L. Disabling Abl-perspectives on Abl kinase regulation and cancer therapeutics. Cancer Cell 1 (2002) 13-15
-
(2002)
Cancer Cell
, vol.1
, pp. 13-15
-
-
Sawyers, C.L.1
-
24
-
-
0033063429
-
Crystal structure of Hck in complex with a Src family-selective tyrosine kinase inhibitor
-
Schindler T., Sicheri F., Pico A., Gazit A., Levitzki A., and Kuriyan J. Crystal structure of Hck in complex with a Src family-selective tyrosine kinase inhibitor. Mol. Cell 3 (1999) 639-648
-
(1999)
Mol. Cell
, vol.3
, pp. 639-648
-
-
Schindler, T.1
Sicheri, F.2
Pico, A.3
Gazit, A.4
Levitzki, A.5
Kuriyan, J.6
-
25
-
-
0034665713
-
Structural mechanism for STI-571 inhibition of abelson tyrosine kinase
-
Schindler T., Bornmann W., Pellicena P., Miller W.T., Clarkson B., and Kuriyan J. Structural mechanism for STI-571 inhibition of abelson tyrosine kinase. Science 289 (2000) 1938-1942
-
(2000)
Science
, vol.289
, pp. 1938-1942
-
-
Schindler, T.1
Bornmann, W.2
Pellicena, P.3
Miller, W.T.4
Clarkson, B.5
Kuriyan, J.6
-
26
-
-
33847659183
-
c-Src binds to the cancer drug imatinib with an inactive Abl/c-Kit conformation and a distributed thermodynamic penalty
-
Seeliger M.A., Nagar B., Frank F., Cao X., Henderson M.N., and Kuriyan J. c-Src binds to the cancer drug imatinib with an inactive Abl/c-Kit conformation and a distributed thermodynamic penalty. Structure 15 (2007) 299-311
-
(2007)
Structure
, vol.15
, pp. 299-311
-
-
Seeliger, M.A.1
Nagar, B.2
Frank, F.3
Cao, X.4
Henderson, M.N.5
Kuriyan, J.6
-
27
-
-
0001686739
-
Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
-
Shah N.P., Nicoll J.M., Nagar B., Gorre M.E., Paquette R.L., Kuriyan J., and Sawyers C.L. Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2 (2002) 117-125
-
(2002)
Cancer Cell
, vol.2
, pp. 117-125
-
-
Shah, N.P.1
Nicoll, J.M.2
Nagar, B.3
Gorre, M.E.4
Paquette, R.L.5
Kuriyan, J.6
Sawyers, C.L.7
-
28
-
-
49649108911
-
Solution conformations and dynamics of ABL kinase-inhibitor complexes determined by NMR substantiate the different binding modes of imatinib/nilotinib and dasatinib
-
Vajpai N., Strauss A., Fendrich G., Cowan-Jacob S.W., Manley P.W., Grzesiek S., and Jahnke W. Solution conformations and dynamics of ABL kinase-inhibitor complexes determined by NMR substantiate the different binding modes of imatinib/nilotinib and dasatinib. J. Biol. Chem. 283 (2008) 18292-18302
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 18292-18302
-
-
Vajpai, N.1
Strauss, A.2
Fendrich, G.3
Cowan-Jacob, S.W.4
Manley, P.W.5
Grzesiek, S.6
Jahnke, W.7
-
29
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
Wan P.T., Garnett M.J., Roe S.M., Lee S., Niculescu-Duvaz D., Good V.M., Jones C.M., Marshall C.J., Springer C.J., Barford D., and Marais R. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell 116 (2004) 855-867
-
(2004)
Cell
, vol.116
, pp. 855-867
-
-
Wan, P.T.1
Garnett, M.J.2
Roe, S.M.3
Lee, S.4
Niculescu-Duvaz, D.5
Good, V.M.6
Jones, C.M.7
Marshall, C.J.8
Springer, C.J.9
Barford, D.10
Marais, R.11
-
30
-
-
0031025991
-
Three-dimensional structure of the tyrosine kinase c-Src
-
Xu W., Harrison S.C., and Eck M.J. Three-dimensional structure of the tyrosine kinase c-Src. Nature 385 (1997) 595-602
-
(1997)
Nature
, vol.385
, pp. 595-602
-
-
Xu, W.1
Harrison, S.C.2
Eck, M.J.3
|