-
1
-
-
27544500981
-
Growing roles for the mTOR pathway
-
DOI 10.1016/j.ceb.2005.09.009, PII S0955067405001481
-
Sarbassov, D. D., Ali, S. M., Sabatini, D. M. (2005) Growing roles for the mTOR pathway. Curr. Opin. Cell Biol. 17, 596-603. (Pubitemid 41540408)
-
(2005)
Current Opinion in Cell Biology
, vol.17
, Issue.6
, pp. 596-603
-
-
Sarbassov, D.D.1
Ali, S.M.2
Sabatini, D.M.3
-
2
-
-
0016713286
-
Rapamycin (AY-22989), a new antifungal antibiotic. II. Fermentation, isolation and characterization
-
Sehgal, S. N.; Baker, H.; Vezina, C. (1975) Rapamycin (AY-22989), a new antifungal antibiotic. II. Fermentation, isolation and characterization. J. antibiotics (Tokyo), 28, 727-732.
-
(1975)
J. Antibiotics (Tokyo)
, vol.28
, pp. 727-732
-
-
Sehgal, S.N.1
Baker, H.2
Vezina, C.3
-
3
-
-
10944261058
-
Mammalian target of rapamycin (mTOR) inhibitors as anti-cancer agents
-
DOI 10.2174/1568009043332718
-
Rao, R. D.; Buckner, J. C.; Sarkaria, J. N. (2004) mammalian Target of Rapamycin (mTOR) Inhibitors as Anti-Cancer Agents. Curr. Cancer Drug. Targets. 4, 621-635. (Pubitemid 40013570)
-
(2004)
Current Cancer Drug Targets
, vol.4
, Issue.8
, pp. 621-635
-
-
Rao, R.D.1
Buckner, J.C.2
Sarkaria, J.N.3
-
4
-
-
34347220473
-
Defining the Role of mTOR in Cancer
-
DOI 10.1016/j.ccr.2007.05.008, PII S1535610807001511
-
Guertin, D. A., Sabatini, D.M. (2007) Defining the role of mTOR in cancer. Cancer cell, 12, 9-22. (Pubitemid 47001784)
-
(2007)
Cancer Cell
, vol.12
, Issue.1
, pp. 9-22
-
-
Guertin, D.A.1
Sabatini, D.M.2
-
5
-
-
34548820978
-
Dissecting the Akt/mammalian target of rapamycin signaling network: Emerging results from the head and neck cancer tissue array initiative
-
DOI 10.1158/1078-0432.CCR-07-1041
-
Molinolo, A. A., Hewitt, S. M., Amornphimoltham, P., Keelawat, S., Rangdaeng, S., Meneses, A. et al (2007) Dissecting the Akt/ mammalian target of rapamycin signaling network: emerging results from the head and neck cancer tissue array initiative. Clin Cancer Res, 13, 4964-4973. (Pubitemid 47502060)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.17
, pp. 4964-4973
-
-
Molinolo, A.A.1
Hewitt, S.M.2
Amornphimoltham, P.3
Keelawat, S.4
Rangdaeng, S.5
Garcia, A.M.6
Raimondi, A.R.7
Jufe, R.8
Itoiz, M.9
Gao, Y.10
Saranath, D.11
Kaleebi, G.S.12
Yoo, G.H.13
Leak, L.14
Myers, E.M.15
Shintani, S.16
Wong, D.17
Massey, H.D.18
Yeudall, W.A.19
Lonardo, F.20
Ensley, J.21
Gutkind, J.S.22
more..
-
6
-
-
40649126759
-
MTOR is activated in the majority of malignant melanomas
-
DOI 10.1038/sj.jid.5701074, PII 5701074
-
Karbowniczek, M., Spittle, C.S., Morrison, T., Wu, H., Henske, E.P. (2008) mTOR is activated in the majority of malignant melanomas. J Invest Dermatol 128, 980-987. (Pubitemid 351374287)
-
(2008)
Journal of Investigative Dermatology
, vol.128
, Issue.4
, pp. 980-987
-
-
Karbowniczek, M.1
Spittle, C.S.2
Morrison, T.3
Wu, H.4
Henske, E.P.5
-
7
-
-
65549167833
-
Targeting the mTOR signaling network for cancer therapy
-
Meric-Bernstam, F., Gonzalez-Angulo, A. M. (2009) Targeting the mTOR signaling network for cancer therapy. J Clin Oncol, 27, 2278-2287.
-
(2009)
J Clin Oncol
, vol.27
, pp. 2278-2287
-
-
Meric-Bernstam, F.1
Gonzalez-Angulo, A.M.2
-
8
-
-
65549145048
-
An ATP competitive mammalian target of rapamycin inhibitor reveals rapamycin-insensitive functions of mTORC1
-
Thoreen, C. C., Kang, S. A., Chang, J. W., Liu, Q., Zhang, J., Gao, Y., et al. (2009) An ATPcompetitive mammalian target of rapamycin inhibitor reveals rapamycin-insensitive functions of mTORC1. J Biol Chem. 284, 8023-8032.
-
(2009)
J Biol Chem.
, vol.284
, pp. 8023-8032
-
-
Thoreen, C.C.1
Kang, S.A.2
Chang, J.W.3
Liu, Q.4
Zhang, J.5
Gao, Y.6
-
9
-
-
33947538050
-
Rapamycin induces feedback activation of Akt signaling through an IGF-1R-dependent mechanism
-
DOI 10.1038/sj.onc.1209990, PII 1209990
-
Wan, X., Harkavy, B., Shen, N., Grohar, P., Helman, L. J. (2007) Rapamycin induces feedback activation of Akt signaling through an IGF-1R-dependent mechanism. Oncogene, 26, 1932-1940. (Pubitemid 46474636)
-
(2007)
Oncogene
, vol.26
, Issue.13
, pp. 1932-1940
-
-
Wan, X.1
Harkavy, B.2
Shen, N.3
Grohar, P.4
Helman, L.J.5
-
10
-
-
0033634827
-
Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine
-
Walker, E. H., Pacold, M. E., Perisic, O., Stephens, L., Hawkins, P. T., Wymann, M. P., et al. (2000) Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine. Mol. Cell, 6, 909-919.
-
(2000)
Mol. Cell
, vol.6
, pp. 909-919
-
-
Walker, E.H.1
Pacold, M.E.2
Perisic, O.3
Stephens, L.4
Hawkins, P.T.5
Wymann, M.P.6
-
11
-
-
33947730475
-
Synthesis and biological evaluation of pyrido[3′,2′:4,5] furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110α inhibitors
-
DOI 10.1016/j.bmcl.2007.02.032, PII S0960894X07002302
-
Hayakawa, M., Kaizawa, H., Moritomo, H., Koizumi, T., Ohishi, T., Yamano, M., et al. (2007) Synthesis and biological evaluation of pyrido[3',2':4,5] furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110alpha inhibitors. Bioorg. Med. Chem. Lett., 17, 2438-2442. (Pubitemid 46507793)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.9
, pp. 2438-2442
-
-
Hayakawa, M.1
Kaizawa, H.2
Moritomo, H.3
Koizumi, T.4
Ohishi, T.5
Yamano, M.6
Okada, M.7
Ohta, M.8
Tsukamoto, S.-i.9
Raynaud, F.I.10
Workman, P.11
Waterfield, M.D.12
Parker, P.13
-
12
-
-
51649088622
-
PI-103, a dual inhibitor of class IA phosphatidylinositide 3-kinase and mTOR, has antileukemic activity in AML
-
Park, S., Chapuis, N., Bardet, V., Tamburini, J., Gallay, N., Willems, L., et al. (2008) PI-103, a dual inhibitor of class IA phosphatidylinositide 3-kinase and mTOR, has antileukemic activity in AML. Leukemia, 22, 1698-1706.
-
(2008)
Leukemia
, vol.22
, pp. 1698-1706
-
-
Park, S.1
Chapuis, N.2
Bardet, V.3
Tamburini, J.4
Gallay, N.5
Willems, L.6
-
13
-
-
67650312583
-
Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR)
-
García-Martínez, J. M., Moran, J., Clarke, R. G., Gray, A., Cosulich, S. C., Chresta, C. M., et al. (2009) Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR). Biochem J, 421, 29-42.
-
(2009)
Biochem J
, vol.421
, pp. 29-42
-
-
García-Martínez, J.M.1
Moran, J.2
Clarke, R.G.3
Gray, A.4
Cosulich, S.C.5
Chresta, C.M.6
-
14
-
-
68049137608
-
Biochemical, cellular, and in vivo activity of novel ATPcompetitive and selective inhibitors of the mammalian target of rapamycin
-
Yu, K., Toral-Barza, L., Shi, C., Zhang, W. G., Lucas, J., Shor, B., et al. (2009) Biochemical, cellular, and in vivo activity of novel ATPcompetitive and selective inhibitors of the mammalian target of rapamycin. Cancer Res. 69, 6232-6240.
-
(2009)
Cancer Res.
, vol.69
, pp. 6232-6240
-
-
Yu, K.1
Toral-Barza, L.2
Shi, C.3
Zhang, W.G.4
Lucas, J.5
Shor, B.6
-
15
-
-
77957870285
-
MTOR medicated anti-cancer drug discovery
-
Liu, Q., Thoreen, C. C., Wang, J., Sabatini, D. M., Gray, N. S. (2009) mTOR medicated anti-cancer drug discovery. Drug. Discov. Today: Therapeutic Strategies. 6, 47-55.
-
(2009)
Drug. Discov. Today: Therapeutic Strategies.
, vol.6
, pp. 47-55
-
-
Liu, Q.1
Thoreen, C.C.2
Wang, J.3
Sabatini, D.M.4
Gray, N.S.5
-
16
-
-
0037181078
-
A combinatorial scaffold approach toward kinase-directed heterocycle libraries
-
DOI 10.1021/ja0170302
-
Ding, S., Gray, N. S., Wu, X., Ding, Q., Schultz, P. G. (2002) A combinatorial scaf-fold approach toward kinase-directed heterocycle libraries. J. Am. Chem. Soc., 124, 1594-1596. (Pubitemid 34173880)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.8
, pp. 1594-1596
-
-
Ding, S.1
Gray, N.S.2
Wu, X.3
Ding, Q.4
Schultz, P.G.5
-
17
-
-
77957903550
-
Discovery of 1-(4-(4-propionylpiperazin-1-yl)-3-(trifluoromethyl)phenyl)- 9-(quinolin-3-yl) benzo[h][1,6]naphthyridin-2(1 H)-one as a highly potent, selective mTOR inhibitor for the treatment of cancer
-
DOI: 10.1021/jm101144f
-
Liu, Q., Chang, J., Wang, J., Kang, S. A., Thoreen, C.C., Markhard, A., Hur, W., Zhang, J., Sim, T., Sabatini, D. M., Gray, N. S. (2010) Discovery of 1-(4-(4-propionylpiperazin-1-yl)-3-(trifluoromethyl)phenyl)-9-(quinolin-3-yl) benzo[h][1,6]naphthyridin-2(1 H)-one as a highly potent, selective mTOR inhibitor for the treatment of cancer. J. Med. Chem. DOI: 10.1021/jm101144f
-
(2010)
J. Med. Chem.
-
-
Liu, Q.1
Chang, J.2
Wang, J.3
Kang, S.A.4
Thoreen, C.C.5
Markhard, A.6
Hur, W.7
Zhang, J.8
Sim, T.9
Sabatini, D.M.10
Gray, N.S.11
-
18
-
-
33751348056
-
Ablation in Mice of the mTORC Components raptor, rictor, or mLST8 Reveals that mTORC2 Is Required for Signaling to Akt-FOXO and PKCα, but Not S6K1
-
DOI 10.1016/j.devcel.2006.10.007, PII S153458070600459X
-
Guertin, D. A., Stevens, D. M., Thoreen, C. C., Burds, A. A., Kalaany, N. Y., Moffat, J., Brown, M., Fitzgerald, K. J., Sabatini, D. M. (2006) Ablation in mice of the mTORC components raptor, rictor, or mLST8 reveals that mTORC2 is required for signaling to Akt-FOXO and PKCalpha, but not S6K1. Dev. Cell, 11, 859-871 (Pubitemid 44804279)
-
(2006)
Developmental Cell
, vol.11
, Issue.6
, pp. 859-871
-
-
Guertin, D.A.1
Stevens, D.M.2
Thoreen, C.C.3
Burds, A.A.4
Kalaany, N.Y.5
Moffat, J.6
Brown, M.7
Fitzgerald, K.J.8
Sabatini, D.M.9
-
19
-
-
76149120388
-
Autodock vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
-
Trott, O., Olson, A. J. (2010) Autodock vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem., 31, 455-461.
-
(2010)
J. Comput. Chem.
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
|