-
1
-
-
84855457952
-
Hsp90 molecular chaperone inhibitors: Are we there yet?
-
Neckers, L.; Workman, P. Hsp90 molecular chaperone inhibitors: are we there yet? Clin. Cancer Res. 2012, 18, 64-76
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 64-76
-
-
Neckers, L.1
Workman, P.2
-
2
-
-
77958516062
-
ATPases as drug targets: Insights from heat shock proteins 70 and 90
-
Massey, A. J. ATPases as drug targets: insights from heat shock proteins 70 and 90 J. Med. Chem. 2010, 53, 7280-7286
-
(2010)
J. Med. Chem.
, vol.53
, pp. 7280-7286
-
-
Massey, A.J.1
-
3
-
-
74849111762
-
Heat shock protein 90: Inhibitors in clinical trials
-
Biamonte, M. A.; Van De Water, R.; Perret, D.; Arndt, J. W.; Scannevin, R. H.; Lee, W.-C. Heat shock protein 90: Inhibitors in clinical trials J. Med. Chem. 2010, 53, 3-17
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3-17
-
-
Biamonte, M.A.1
Van De Water, R.2
Perret, D.3
Arndt, J.W.4
Scannevin, R.H.5
Lee, W.-C.6
-
4
-
-
84872613169
-
-
HSP90 Interactors
-
HSP90 Interactors. http://www.picard.ch/downloads/Hsp90interactors.pdf.
-
-
-
-
5
-
-
0029123128
-
ErbB-2 oncogene inhibition by geldanamycin derivatives: Synthesis, mechanism of action, and structure-activity relationships
-
Schnur, R. C.; Corman, M. L.; Gallaschun, R. J.; Cooper, B. A.; Dee, M. F.; Doty, J. L.; Muzzi, M. L.; DiOrio, C. I.; Barbacci, E. G.; Miller, P. E.; Pollack, V. A.; Savage, D. M.; Sloan, D. E.; Pustilnik, L. R.; Moyer, J. D.; Moyer, M. P. erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships J. Med. Chem. 1995, 38, 3813-3820
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3813-3820
-
-
Schnur, R.C.1
Corman, M.L.2
Gallaschun, R.J.3
Cooper, B.A.4
Dee, M.F.5
Doty, J.L.6
Muzzi, M.L.7
Diorio, C.I.8
Barbacci, E.G.9
Miller, P.E.10
Pollack, V.A.11
Savage, D.M.12
Sloan, D.E.13
Pustilnik, L.R.14
Moyer, J.D.15
Moyer, M.P.16
-
6
-
-
33746662241
-
Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90
-
DOI 10.1021/jm0603116
-
Ge, J.; Normant, E.; Porter, J. R.; Ali, J. A.; Dembski, M. S.; Gao, Y.; Georges, A. T.; Grenier, L.; Pak, R. H.; Patterson, J.; Sydor, J. R.; Tibbits, T. T.; Tong, J. K.; Adams, J.; Palombella, V. J. Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17- demethoxygeldanamycin as potent, water-soluble inhibitors of HSP90 J. Med. Chem. 2006, 49, 4606-4615 (Pubitemid 44162687)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.15
, pp. 4606-4615
-
-
Ge, J.1
Normant, E.2
Porter, J.R.3
Ali, J.A.4
Dembski, M.S.5
Gao, Y.6
Georges, A.T.7
Grenier, L.8
Pak, R.H.9
Patterson, J.10
Sydor, J.R.11
Tibbitts, T.T.12
Tong, J.K.13
Adams, J.14
Palombella, V.J.15
-
7
-
-
19944427585
-
Dose range-finding toxicity studies of 17-DMAG
-
Glaze, E. R.; Smith, A. C.; Johnson, D. W.; McCormick, D. L.; Brown, A. B.; Levin, B. S.; Krishnaraj, R.; Lyubimov, A.; Egorin, M. J.; Tomaszewski, J. E. Dose range-finding toxicity studies of 17-DMAG Proc. Am. Assoc. Cancer Res. 2003, 44, 162-162
-
(2003)
Proc. Am. Assoc. Cancer Res.
, vol.44
, pp. 162-162
-
-
Glaze, E.R.1
Smith, A.C.2
Johnson, D.W.3
McCormick, D.L.4
Brown, A.B.5
Levin, B.S.6
Krishnaraj, R.7
Lyubimov, A.8
Egorin, M.J.9
Tomaszewski, J.E.10
-
8
-
-
11244337455
-
Pharmacokinetics and pharmacodynamics of 17-demethoxy 17-[[(2- dimethylamino)ethyl]amino]geldanamycin (17DMAG, NSC 707545) in C.B-17 SCID mice bearing MDA-MB-231 human breast cancer xenografts
-
DOI 10.1007/s00280-004-0865-3
-
Eiseman, J. L.; Lan, J.; Lagatutta, T. F.; Hamburger, D. R.; Joseph, E.; Covey, J. M.; Egorin, M. J. Pharmacokinetics and pharmacodynamics of 17-demethoxy 17-[[(2-dimethylamino)ethyl]amino]geldanamycin (17DMAG, NSC 707545) in C.B-17 SCID mice bearing MDA-MB-231 human breast cancer xenografts Cancer Chemother. Pharmacol. 2005, 55, 21-32 (Pubitemid 40064492)
-
(2005)
Cancer Chemotherapy and Pharmacology
, vol.55
, Issue.1
, pp. 21-32
-
-
Eiseman, J.L.1
Lan, J.2
Lagattuta, T.F.3
Hamburger, D.R.4
Joseph, E.5
Covey, J.M.6
Egorin, M.J.7
-
9
-
-
84872619170
-
-
IPI-493, a Potent, Orally Bioavailable Hsp90 Inhibitor of the Ansamycin Class
-
IPI-493, a Potent, Orally Bioavailable Hsp90 Inhibitor of the Ansamycin Class. http://infi.com/pipeline-archives/IPI-493%20EORTC%202008.pdf.
-
-
-
-
10
-
-
38349157746
-
4,5-Diarylisoxazole HSP90 chaperone inhibitors: Potential therapeutic agents for the treatment of cancer
-
Brough, P. A.; Aherne, W.; Barril, X.; Borgognoni, J.; Boxall, K.; Cansfield, J. E.; Cheung, K.-M. J.; Collins, I.; Davies, N. G. M.; Drysdale, M. J.; Dymock, B.; Eccles, S. A.; Finch, H.; Fink, A.; Hayes, A.; Howes, R.; Hubbard, R. E.; James, K.; Jordan, A. M.; Lockie, A.; Martins, V.; Massey, A.; Matthews, T. P.; McDonald, E.; Northfield, C. J.; Pearl, L. H.; Prodromou, C.; Ray, S.; Raynaud, F. I.; Roughley, S. D.; Sharp, S. Y.; Surgenor, A.; Walmsley, D. L.; Webb, P.; Wood, M.; Workman, P.; Wright, L. 4,5-Diarylisoxazole HSP90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer J. Med. Chem. 2008, 51, 196-218
-
(2008)
J. Med. Chem.
, vol.51
, pp. 196-218
-
-
Brough, P.A.1
Aherne, W.2
Barril, X.3
Borgognoni, J.4
Boxall, K.5
Cansfield, J.E.6
Cheung, K.-M.J.7
Collins, I.8
Davies, N.G.M.9
Drysdale, M.J.10
Dymock, B.11
Eccles, S.A.12
Finch, H.13
Fink, A.14
Hayes, A.15
Howes, R.16
Hubbard, R.E.17
James, K.18
Jordan, A.M.19
Lockie, A.20
Martins, V.21
Massey, A.22
Matthews, T.P.23
McDonald, E.24
Northfield, C.J.25
Pearl, L.H.26
Prodromou, C.27
Ray, S.28
Raynaud, F.I.29
Roughley, S.D.30
Sharp, S.Y.31
Surgenor, A.32
Walmsley, D.L.33
Webb, P.34
Wood, M.35
Workman, P.36
Wright, L.37
more..
-
11
-
-
77955873344
-
Discovery of (2,4-dihydroxy-5-isopropylphenyl)-[5-(4-methylpiperazin-1- yl-methyl)-1,3-dihydroisondol-2-yl]methanone (AT13387), a novel inhibitor of the molecular chaperone Hsp90 by fragment based drug design
-
Woodhead, A. J; Angove, H.; Carr, M. G.; Chessari, G.; Congreve, M.; Coyle, J. E.; Cosme, J.; Graham, B.; Day, P. J.; Downham, R.; Fazal, L.; Feltell, R.; Figueroa, E.; Frederickson, M.; Lewis, J.; McMenamin, R.; Murray, C. W.; O'Brien, M. A.; Parra, L.; Patel, S.; Phillips, T.; Rees, D. C.; Rich, S.; Smith, D.-M.; Trewartha, G.; Vimkovic, M.; Williams, B.; Woolford, A. J. Discovery of (2,4-dihydroxy-5-isopropylphenyl)-[5-(4-methylpiperazin-1-yl- methyl)-1,3-dihydroisondol-2-yl]methanone (AT13387), a novel inhibitor of the molecular chaperone Hsp90 by fragment based drug design J. Med. Chem. 2010, 53, 5956-5969
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5956-5969
-
-
Woodhead, A.J.1
Angove, H.2
Carr, M.G.3
Chessari, G.4
Congreve, M.5
Coyle, J.E.6
Cosme, J.7
Graham, B.8
Day, P.J.9
Downham, R.10
Fazal, L.11
Feltell, R.12
Figueroa, E.13
Frederickson, M.14
Lewis, J.15
McMenamin, R.16
Murray, C.W.17
O'Brien, M.A.18
Parra, L.19
Patel, S.20
Phillips, T.21
Rees, D.C.22
Rich, S.23
Smith, D.-M.24
Trewartha, G.25
Vimkovic, M.26
Williams, B.27
Woolford, A.J.28
more..
-
12
-
-
84856832510
-
Ganetespib, a unique triazolone-containing Hsp90 inhibitor, exhibits potent antitumor activity and a superior safety profile for cancer therapy
-
Ying, W.; Du, Z.; Sun, L.; Foley, K. P.; Proia, D. A.; Blackman, R. K.; Zhou, D.; Inoue, T.; Tatsuta, N.; Sang, J.; Ye, S.; Acquaviva, J.; Ogawa, L. S.; Wada, Y.; Barsoum, J.; Koya, K. Ganetespib, a unique triazolone-containing Hsp90 inhibitor, exhibits potent antitumor activity and a superior safety profile for cancer therapy Mol. Cancer Ther. 2012, 11, 475-484
-
(2012)
Mol. Cancer Ther.
, vol.11
, pp. 475-484
-
-
Ying, W.1
Du, Z.2
Sun, L.3
Foley, K.P.4
Proia, D.A.5
Blackman, R.K.6
Zhou, D.7
Inoue, T.8
Tatsuta, N.9
Sang, J.10
Ye, S.11
Acquaviva, J.12
Ogawa, L.S.13
Wada, Y.14
Barsoum, J.15
Koya, K.16
-
13
-
-
77952383375
-
New molecular and biological mechanism of antitumor activities of KW-2478, a novel nonansamycin heat shock protein 90 inhibitor, in multiple myeloma cells
-
Nakashima, T.; Ishii, T.; Tagaya, H.; Seike, T.; Nakagawa, H.; Kanda, Y.; Akinaga, S.; Soga, S.; Shiotsu, Y. New molecular and biological mechanism of antitumor activities of KW-2478, a novel nonansamycin heat shock protein 90 inhibitor, in multiple myeloma cells Clin. Cancer Res. 2010, 16, 2792-2802
-
(2010)
Clin. Cancer Res.
, vol.16
, pp. 2792-2802
-
-
Nakashima, T.1
Ishii, T.2
Tagaya, H.3
Seike, T.4
Nakagawa, H.5
Kanda, Y.6
Akinaga, S.7
Soga, S.8
Shiotsu, Y.9
-
14
-
-
33746914732
-
Structural and quantum chemical studies of 8-aryl-sulfanyl adenine class Hsp90 inhibitors
-
DOI 10.1021/jm060297x
-
Immormino, R. M; Kang, Y.; Chiosis, G.; Gewirth, D. T. Structural and quantum chemical studies of 8-aryl-sulfanyl adenine class Hsp90 inhibitors J. Med. Chem. 2006, 49, 4953-4960 (Pubitemid 44201053)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.16
, pp. 4953-4960
-
-
Immormino, R.M.1
Kang, Y.2
Chiosis, G.3
Gewirth, D.T.4
-
15
-
-
66249138886
-
Hsp90 inhibitor PU-H71, a multimodal inhibitor of malignancy, induces complete responses in triple-negative breast cancer models
-
Caldas-Lopes, E.; Cerchietti, L.; Ahn, J. H.; Clement, C. C.; Robles, A. I.; Rodina, A.; Moulick, K.; Taldone, T.; Gozman, A.; Guo, Y.; Wu, N.; de Stanchina, E.; White, J.; Gross, S. S.; Ma, Y.; Varticovski, L.; Melnick, A.; Chiosis, G. Hsp90 inhibitor PU-H71, a multimodal inhibitor of malignancy, induces complete responses in triple-negative breast cancer models Proc. Natl. Acad. Sci. U.S.A. 2009, 106, 8368-8373
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 8368-8373
-
-
Caldas-Lopes, E.1
Cerchietti, L.2
Ahn, J.H.3
Clement, C.C.4
Robles, A.I.5
Rodina, A.6
Moulick, K.7
Taldone, T.8
Gozman, A.9
Guo, Y.10
Wu, N.11
De Stanchina, E.12
White, J.13
Gross, S.S.14
Ma, Y.15
Varticovski, L.16
Melnick, A.17
Chiosis, G.18
-
16
-
-
67449138839
-
CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacologic properties for cancer therapy
-
Bao, R.; Lai, C.-J.; Qu, H.; Wang, D.; Yin, L.; Zifcak, B.; Atoyan, R.; Wang, J.; Samson, M.; Forrester, J.; Della Rocca, S.; Xu, G.-X.; Tao, X.; Zhai, H.-X.; Cai, X.; Qian, C. CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacologic properties for cancer therapy Clin. Cancer Res. 2009, 15, 4046-4057
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 4046-4057
-
-
Bao, R.1
Lai, C.-J.2
Qu, H.3
Wang, D.4
Yin, L.5
Zifcak, B.6
Atoyan, R.7
Wang, J.8
Samson, M.9
Forrester, J.10
Della Rocca, S.11
Xu, G.-X.12
Tao, X.13
Zhai, H.-X.14
Cai, X.15
Qian, C.16
-
17
-
-
84872606102
-
-
Evaluation of the Pharmacokinetics and Efficacy of a Novel Pro-Drug of the HSP90 Inhibitor
-
Evaluation of the Pharmacokinetics and Efficacy of a Novel Pro-Drug of the HSP90 Inhibitor. http://www.myriadpharma.com/images/stories/product- pipeline/mpc-3100/AACR%202011/aacr-2011-abst3237-mpc-3100-prodrug-mpc-0767.pdf.
-
-
-
-
18
-
-
77955444211
-
Application of chemoproteomics to drug discovery: Identification of a clinical candidate targeting hsp90
-
Fadden, P.; Huang, K. H.; Veal, J. M.; Steed, P. M.; Barabasz, A. F.; Foley, B.; Hu, M.; Partridge, J. M.; Rice, J.; Scott, A.; Dubois, L. G.; Freed, T. A.; Silinski, M. A.; Barta, T. E.; Hughes, P. F.; Ommen, A.; Ma, W.; Smith, E. D.; Spangenberg, A. W.; Eaves, J.; Hanson, G. J.; Hinkley, L.; Jenks, M.; Lewis, M.; Otto, J.; Pronk, G. J.; Verleysen, K.; Haystead, T. A.; Hall, S. E. Application of chemoproteomics to drug discovery: identification of a clinical candidate targeting hsp90 Chem. Biol. 2010, 17, 686-694
-
(2010)
Chem. Biol.
, vol.17
, pp. 686-694
-
-
Fadden, P.1
Huang, K.H.2
Veal, J.M.3
Steed, P.M.4
Barabasz, A.F.5
Foley, B.6
Hu, M.7
Partridge, J.M.8
Rice, J.9
Scott, A.10
Dubois, L.G.11
Freed, T.A.12
Silinski, M.A.13
Barta, T.E.14
Hughes, P.F.15
Ommen, A.16
Ma, W.17
Smith, E.D.18
Spangenberg, A.W.19
Eaves, J.20
Hanson, G.J.21
Hinkley, L.22
Jenks, M.23
Lewis, M.24
Otto, J.25
Pronk, G.J.26
Verleysen, K.27
Haystead, T.A.28
Hall, S.E.29
more..
-
19
-
-
34250877881
-
Rationally designed high-affinity 2-amino-6-halopurine heat shock protein 90 inhibitors that exhibit potent antitumor activity
-
DOI 10.1021/jm050752+
-
Kasibhatla, S. R.; Hong, K.; Biamonte, M. A.; Busch, D. J.; Karjian, P. L.; Sensintaffar, J. L.; Kamal, A.; Lough, R. E.; Brekken, J.; Lundgren, K.; Grecko, R.; Timony, G. A.; Ran, Y.; Mansfield, R.; Fritz, L. C.; Ulm, E.; Burrows, F. J.; Boehm, M. F. Rationally designed high-affinity 2-amino-6-halopurine heat shock protein 90 inhibitors that exhibit potent antitumor activity J. Med. Chem. 2007, 50, 2767-2778 (Pubitemid 46980848)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.12
, pp. 2767-2778
-
-
Kasibhatla, S.R.1
Hong, K.2
Biamonte, M.A.3
Busch, D.J.4
Karjian, P.L.5
Sensintaffar, J.L.6
Kamal, A.7
Lough, R.E.8
Brekken, J.9
Lundgren, K.10
Grecko, R.11
Timony, G.A.12
Ran, Y.13
Mansfield, R.14
Fritz, L.C.15
Ulm, E.16
Burrows, F.J.17
Boehm, M.F.18
-
20
-
-
84859379802
-
The novel oral Hsp90 inhibitor NVP-HSP990 exhibits potent and broad-spectrum antitumor activities in vitro and in vivo
-
Menezes, D. L.; Taverna, P.; Jensen, M. R.; Abrams, T.; Stuart, D.; Yu, G. K.; Duhl, D.; Machajewski, T.; Sellers, W. R.; Pryer, N. K.; Gao, Z. The novel oral Hsp90 inhibitor NVP-HSP990 exhibits potent and broad-spectrum antitumor activities in vitro and in vivo Mol. Cancer Ther. 2012, 11, 730-739
-
(2012)
Mol. Cancer Ther.
, vol.11
, pp. 730-739
-
-
Menezes, D.L.1
Taverna, P.2
Jensen, M.R.3
Abrams, T.4
Stuart, D.5
Yu, G.K.6
Duhl, D.7
MacHajewski, T.8
Sellers, W.R.9
Pryer, N.K.10
Gao, Z.11
-
21
-
-
77950807945
-
Preclinical antitumor activity of the orally available heat shock protein 90 inhibitor NVP-BEP800
-
For another series, also from Novartis, see the following
-
For another series, also from Novartis, see the following: Massey, A. J.; Schoepfer, J.; Brough, P. A.; Brueggen, J.; Chene, P.; Drysdale, M. J.; Pfaar, U.; Radimerski, T.; Ruetz, S.; Schweitzer, A.; Wood, M.; Garcia-Echeverria, C.; Jensen, M. R. Preclinical antitumor activity of the orally available heat shock protein 90 inhibitor NVP-BEP800 Mol. Cancer Ther. 2010, 9, 906-919
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 906-919
-
-
Massey, A.J.1
Schoepfer, J.2
Brough, P.A.3
Brueggen, J.4
Chene, P.5
Drysdale, M.J.6
Pfaar, U.7
Radimerski, T.8
Ruetz, S.9
Schweitzer, A.10
Wood, M.11
Garcia-Echeverria, C.12
Jensen, M.R.13
-
22
-
-
79960985354
-
Hsp90 inhibition is effective in breast cancer: A phase II trial of tanespimycin (17-AAG) plus trastuzumab in patients with Her-2 positive metastatic breast cancer progressing on trastuzumab
-
Modi, S.; Stopeck, A.; Linden, A.; Solit, D.; Chandarlapaty, S.; Rosen, N.; D'Andrea, G.; Dickler, M.; Moynahan, M. E.; Sugarman, S.; Ma, W.; Patil, S.; Norton, L.; Hannan, A. L.; Hudis, C. Hsp90 inhibition is effective in breast cancer: a phase II trial of tanespimycin (17-AAG) plus trastuzumab in patients with Her-2 positive metastatic breast cancer progressing on trastuzumab Clin. Cancer Res. 2011, 17, 5132-5139
-
(2011)
Clin. Cancer Res.
, vol.17
, pp. 5132-5139
-
-
Modi, S.1
Stopeck, A.2
Linden, A.3
Solit, D.4
Chandarlapaty, S.5
Rosen, N.6
D'Andrea, G.7
Dickler, M.8
Moynahan, M.E.9
Sugarman, S.10
Ma, W.11
Patil, S.12
Norton, L.13
Hannan, A.L.14
Hudis, C.15
-
23
-
-
84872620315
-
-
Presented at the ASCO Annual Meeting
-
Wong, K. K.; Koczywas, M.; Goldman, J. W.; Paschold, E. H.; Horn, L.; Lufkin, J. M.; Kepros, J.; Teofilici, F.; Shapiro, G.; Socinski, M. A. An Open-Label Phase II Study of the Hsp90 Inhibitor Ganetespib. (STA-9090) as Monotherapy in Patients with Advanced NSCLC. Presented at the ASCO Annual Meeting, 2011; http://www.syntapharma.com/Documents/Ganetespib- Phase%202%20NSCLC-Shapiro-ASCO%202011.pdf.
-
(2011)
An Open-Label Phase II Study of the Hsp90 Inhibitor Ganetespib. (STA-9090) As Monotherapy in Patients with Advanced NSCLC
-
-
Wong, K.K.1
Koczywas, M.2
Goldman, J.W.3
Paschold, E.H.4
Horn, L.5
Lufkin, J.M.6
Kepros, J.7
Teofilici, F.8
Shapiro, G.9
Socinski, M.A.10
-
24
-
-
79951885125
-
Activity of IPI-504, a novel heat-shock protein 90 inhibitor, in patients with molecularly defined non-small-cell lung cancer
-
Sequist, L. V.; Gettinger, S.; Senzer, N. N.; Martins, R. G.; Jänne, P. A.; Lilenbaum, R.; Gray, J. E.; Iafrate, A. J.; Katayama, R.; Hafeez, N.; Sweeney, J.; Walker, J. R.; Fritz, C.; Ross, R. W.; Grayzel, D.; Engelman, J. A.; Borger, D. R.; Paez, G.; Natale, R. Activity of IPI-504, a novel heat-shock protein 90 inhibitor, in patients with molecularly defined non-small-cell lung cancer J. Clin. Oncol. 2010, 28, 4953-4960
-
(2010)
J. Clin. Oncol.
, vol.28
, pp. 4953-4960
-
-
Sequist, L.V.1
Gettinger, S.2
Senzer, N.N.3
Martins, R.G.4
Jänne, P.A.5
Lilenbaum, R.6
Gray, J.E.7
Iafrate, A.J.8
Katayama, R.9
Hafeez, N.10
Sweeney, J.11
Walker, J.R.12
Fritz, C.13
Ross, R.W.14
Grayzel, D.15
Engelman, J.A.16
Borger, D.R.17
Paez, G.18
Natale, R.19
-
25
-
-
79956318797
-
Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK
-
Katayama, R.; Khan, T. M.; Benes, C.; Lifshits, E.; Ebi, H.; Rivera, V. M.; Shakespeare, W. C.; Iafrate, A. J.; Engelman, J. A.; Shaw, A. T. Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK Proc. Natl. Acad. Sci. U.S.A. 2011, 108, 7535-7540
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 7535-7540
-
-
Katayama, R.1
Khan, T.M.2
Benes, C.3
Lifshits, E.4
Ebi, H.5
Rivera, V.M.6
Shakespeare, W.C.7
Iafrate, A.J.8
Engelman, J.A.9
Shaw, A.T.10
-
26
-
-
79957539428
-
Tanespimycin and bortezomib combination treatment in patients with relapsed or relapsed and refractory multiple myeloma: Results of a phase 1/2 study
-
Richardson, P G.; Chanan-Khan, A. A.; Lonial, S.; Krishnan, A. Y.; Carroll, M. P.; Alsina, M.; Albitar, M.; Berman, D.; Messina, M.; Anderson, K. C. Tanespimycin and bortezomib combination treatment in patients with relapsed or relapsed and refractory multiple myeloma: results of a phase 1/2 study Br. J. Haematol. 2011, 153, 729-740
-
(2011)
Br. J. Haematol.
, vol.153
, pp. 729-740
-
-
Richardson, P.G.1
Chanan-Khan, A.A.2
Lonial, S.3
Krishnan, A.Y.4
Carroll, M.P.5
Alsina, M.6
Albitar, M.7
Berman, D.8
Messina, M.9
Anderson, K.C.10
-
27
-
-
78851472038
-
Inhibition of heat shock protein 90 (HSP90) as a therapeutic strategy for the treatment of myeloma and other cancers
-
Richardson, P. G.; Mitsiades, C. S.; Laubach, J. P.; Lonial, S.; Chanan-Khan, A. A; Anderson, K. C. Inhibition of heat shock protein 90 (HSP90) as a therapeutic strategy for the treatment of myeloma and other cancers Br. J. Haematol. 2011, 152, 367-379
-
(2011)
Br. J. Haematol.
, vol.152
, pp. 367-379
-
-
Richardson, P.G.1
Mitsiades, C.S.2
Laubach, J.P.3
Lonial, S.4
Chanan-Khan, A.A.5
Anderson, K.C.6
-
28
-
-
74049091229
-
BIIB021, a novel Hsp90 inhibitor, sensitized head and neck squamous cell carcinoma to radiotherapy
-
Yin, Z.; Zhang, H.; Lundgren, K.; Wilson, L.; Burrows, F.; Shores, C. G. BIIB021, a novel Hsp90 inhibitor, sensitized head and neck squamous cell carcinoma to radiotherapy Int. J. Cancer 2010, 126, 1216-1225
-
(2010)
Int. J. Cancer
, vol.126
, pp. 1216-1225
-
-
Yin, Z.1
Zhang, H.2
Lundgren, K.3
Wilson, L.4
Burrows, F.5
Shores, C.G.6
-
29
-
-
84860457656
-
Phase 1 dose escalation study of the oral heat shock protein 90 (Hsp90) inhibitor PF-04929113/SNX-5422 (PF-113) and its associated ocular toxicity
-
Infante, J.; Weiss, G.; Jones, S.; Tibes, R.; Bendell, J.; Brega, N.; Torti, V.; Von Hoff, D.; Burris, H., III; Ramanathan, R. Phase 1 dose escalation study of the oral heat shock protein 90 (Hsp90) inhibitor PF-04929113/SNX-5422 (PF-113) and its associated ocular toxicity EJC Suppl. 2010, 8, 119
-
(2010)
EJC Suppl.
, vol.8
, pp. 119
-
-
Infante, J.1
Weiss, G.2
Jones, S.3
Tibes, R.4
Bendell, J.5
Brega, N.6
Torti, V.7
Von Hoff, D.8
Burris III, H.9
Ramanathan, R.10
-
30
-
-
67650734421
-
-
WO 2006/091963
-
Huang, K. H.; Eaves, J.; Veal, J.; Barta, T.; Lifeng, G.; Hinkley, L.; Hanson, G. Tetrahydroindolone and Tetrahydroindazolone Derivatives, WO 2006/091963, 2006.
-
(2006)
Tetrahydroindolone and Tetrahydroindazolone Derivatives
-
-
Huang, K.H.1
Eaves, J.2
Veal, J.3
Barta, T.4
Lifeng, G.5
Hinkley, L.6
Hanson, G.7
-
31
-
-
84866312264
-
-
US 2007/0207984
-
Huang, K. H.; Eaves, J.; Veal, J.; Hall, S. E.; Barta, T. E.; Hanson, G. J. Cyclohexylamino Benzene, Pyridine, and Pyridazine Derivatives. US 2007/0207984, 2007.
-
(2007)
Cyclohexylamino Benzene, Pyridine, and Pyridazine Derivatives
-
-
Huang, K.H.1
Eaves, J.2
Veal, J.3
Hall, S.E.4
Barta, T.E.5
Hanson, G.J.6
-
32
-
-
66449094961
-
BIIB021, an orally available, fully synthetic small molecule inhibitor of the heat shock protein HSP90
-
Lundgren, K.; Zhang, H.; Brekken, J.; Huser, N.; Powell, R. E.; Timple, N.; Busch, D. J.; Neely, L.; Sensintaffar, J. L.; Yang, Y.-C.; McKenzie, A.; Friedman, J.; Scannevin, R.; Kamal, A.; Hong, K.; Kasibhatla, S. R.; Boehm, M. F.; Burrows, F. J. BIIB021, an orally available, fully synthetic small molecule inhibitor of the heat shock protein HSP90 Mol. Cancer Ther. 2009, 8, 921-929
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 921-929
-
-
Lundgren, K.1
Zhang, H.2
Brekken, J.3
Huser, N.4
Powell, R.E.5
Timple, N.6
Busch, D.J.7
Neely, L.8
Sensintaffar, J.L.9
Yang, Y.-C.10
McKenzie, A.11
Friedman, J.12
Scannevin, R.13
Kamal, A.14
Hong, K.15
Kasibhatla, S.R.16
Boehm, M.F.17
Burrows, F.J.18
-
33
-
-
0037011902
-
Structure-based design and characterization of novel platforms for ricin and shiga toxin inhibition
-
DOI 10.1021/jm010186s
-
Miller, D. J.; Ravikumar, K.; Shen, H.; Suh, J.-K.; Kerwin, S. M.; Robertus, J. D. Structure-based and characterization of novel platforms for ricin and shiga toxin inhibition J. Med. Chem. 2002, 45, 90-98 (Pubitemid 34038544)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.1
, pp. 90-98
-
-
Miller, D.J.1
Ravikumar, K.2
Shen, H.3
Suh, J.-K.4
Kerwin, S.M.5
Robertus, J.D.6
-
34
-
-
0026494947
-
A dideazatetrahydrofolate analog lacking a chiral center at C-6: N -[4-[2-(2-amino-3,4-dihydro-4-oxo-7 H -pyrrolo[2,3- d ]pyrimidin-5yl) ethyl[benzoyl]- l -glutamic acid is an inhibitor of thymidylate synthase
-
Taylor, E. C.; Kuhnt, D.; Shih, C.; Rinzel, S. M.; Grindey, G. B.; Barredo, J.; Jannatipour, M.; Moran, R. G. A dideazatetrahydrofolate analog lacking a chiral center at C-6: N -[4-[2-(2-amino-3,4-dihydro-4-oxo-7 H -pyrrolo[2,3- d ]pyrimidin-5yl)ethyl[benzoyl]- l -glutamic acid is an inhibitor of thymidylate synthase J. Med. Chem. 1992, 35, 4450-4454
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4450-4454
-
-
Taylor, E.C.1
Kuhnt, D.2
Shih, C.3
Rinzel, S.M.4
Grindey, G.B.5
Barredo, J.6
Jannatipour, M.7
Moran, R.G.8
-
35
-
-
0037434508
-
Design, synthesis, and biological activities of classical N-{4-[2-(2-amino-4-ethylpyrrolo[2,3-d]pyrimidin-5-yl)ethyl] benzoyl}-L-glutamic acid and its 6-methyl derivative as potential dual inhibitors of thymidylate synthase and dihydrofolate reductase and as potential antitumor agents
-
DOI 10.1021/jm0203534
-
Gangjee, A.; Yu, J.; Kisliuk, R. L.; Haile, W. H.; Sobrero, G.; McGuire, J. J. Design, synthesis, and biological activities of classical N -{4-[2-(2-amino-4-ethylpyrrolo[2,3- d ]pyrimidin-5-yl)ethyl]benzoyl}- l -glutamic acid and its 6-methyl derivative as potential dual inhibitors of thymidylate synthase and dihydrofolate reductase as potential antitumor agents J. Med. Chem. 2003, 46, 591-600 (Pubitemid 36182760)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.4
, pp. 591-600
-
-
Gangjee, A.1
Yu, J.2
Kisliuk, R.L.3
Haile, W.H.4
Sobrero, G.5
McGuire, J.J.6
-
36
-
-
0000262710
-
The synthesis of N -{2-amino-4-substituted [(pyrrolo[2,3- d ]pyrimidin-5-yl)ethyl]benzoyl}- l -glutamic acids as antineoplastic agents
-
Shih, C.; Gossett, L. S. The synthesis of N -{2-amino-4-substituted [(pyrrolo[2,3- d ]pyrimidin-5-yl)ethyl]benzoyl}- l -glutamic acids as antineoplastic agents Heterocycles 1993, 35, 825-841
-
(1993)
Heterocycles
, vol.35
, pp. 825-841
-
-
Shih, C.1
Gossett, L.S.2
-
37
-
-
2942711907
-
Regioselective syntheses of 7-halogenated 7-deazapurine nucleosides related to 2-amino-7-deaza-2′-deoxyadenosine and 7-deaza-2′- deoxyisoguanosine
-
Seela, F.; Peng, X. Regioselective syntheses of 7-halogenated 7-deazapurine nucleosides related to 2-amino-7-deaza-2′-deoxyadenosine and 7-deaza-2′-deoxyisoguanosine Synthesis 2004, 1203-1210 (Pubitemid 38789300)
-
(2004)
Synthesis
, Issue.8
, pp. 1203-1210
-
-
Seela, F.1
Peng, X.2
-
38
-
-
84993848939
-
A convenient method for regioselective C-5 halogenation of 4(3 H)-oxo-7 H -pyrrolo[2,3- d ]pyrimidines
-
Barnett, C. J.; Kobierski, M. E. A convenient method for regioselective C-5 halogenation of 4(3 H)-oxo-7 H -pyrrolo[2,3- d ]pyrimidines J. Heterocycl. Chem. 1994, 31, 1181-1183
-
(1994)
J. Heterocycl. Chem.
, vol.31
, pp. 1181-1183
-
-
Barnett, C.J.1
Kobierski, M.E.2
-
39
-
-
0033708968
-
Synthesis and stereochemistry of insect derived spiroacetals with branched carbon skeletons
-
Tu, Y. Q.; Huebener, A.; Zhang, H.; Moore, C. J.; Fletcher, M. T.; Hayes, P.; Dettner, K.; Francke, W.; McErlean, C. S. P.; Kitching, W. Synthesis and stereochemistry of insect derived spiroacetals with branched carbon skeletons Synthesis 2000, 13, 1956-1978
-
(2000)
Synthesis
, vol.13
, pp. 1956-1978
-
-
Tu, Y.Q.1
Huebener, A.2
Zhang, H.3
Moore, C.J.4
Fletcher, M.T.5
Hayes, P.6
Dettner, K.7
Francke, W.8
McErlean, C.S.P.9
Kitching, W.10
-
40
-
-
79251588744
-
EC144, a synthetic inhibitor of heat shock protein 90, blocks innate and adaptive immune responses in models of inflammation and autoimmunity
-
Yun, T. J.; Harning, E. K.; Giza, K.; Rabah, D.; Li, P.; Arndt, J. W.; Luchetti, D.; Biamonte, M. A.; Shi, J.; Lundgren, K.; Manning, A.; Kehry, M. R. EC144, a synthetic inhibitor of heat shock protein 90, blocks innate and adaptive immune responses in models of inflammation and autoimmunity J. Immunol. 2011, 186, 563-575
-
(2011)
J. Immunol.
, vol.186
, pp. 563-575
-
-
Yun, T.J.1
Harning, E.K.2
Giza, K.3
Rabah, D.4
Li, P.5
Arndt, J.W.6
Luchetti, D.7
Biamonte, M.A.8
Shi, J.9
Lundgren, K.10
Manning, A.11
Kehry, M.R.12
-
41
-
-
34547638990
-
Chemogenomic analysis identifies geldanamycins as substrates and inhibitors of ABCB1
-
DOI 10.1007/s11095-007-9300-x
-
Huang, Y.; Blower, P. E.; Liu, R.; Dai, Z.; Pham, A. N.; Moon, H.; Fang, J.; Sadée, W. Chemogenomic analysis indentifies geldanamycins as substrated and inhibitors of ABCB1 Pharm. Res. 2007, 9, 1702-1712 (Pubitemid 47206620)
-
(2007)
Pharmaceutical Research
, vol.24
, Issue.9
, pp. 1702-1712
-
-
Huang, Y.1
Blower, P.E.2
Liu, R.3
Dai, Z.4
Pham, A.-N.5
Moon, H.6
Fang, J.7
Sadee, W.8
-
42
-
-
74049114496
-
BIIB021, a synthetic Hsp90 inhibitor, has broad application against tumors with acquired multidrug resistance
-
Zhang, H.; Neely, L.; Yang, Y.-C.; Timple, N.; Burrows, F. BIIB021, a synthetic Hsp90 inhibitor, has broad application against tumors with acquired multidrug resistance Int. J. Cancer 2009, 126, 1226-1234
-
(2009)
Int. J. Cancer
, vol.126
, pp. 1226-1234
-
-
Zhang, H.1
Neely, L.2
Yang, Y.-C.3
Timple, N.4
Burrows, F.5
-
43
-
-
57449113371
-
Heat shock protein 90: Translation from cancer to Alzheimer's disease treatment?
-
Luo, W.; Rodina, A.; Chiosis, G. Heat shock protein 90: translation from cancer to Alzheimer's disease treatment? BMC Neurosci. 2008, 9 (Suppl. 2) S7
-
(2008)
BMC Neurosci.
, vol.9
, Issue.SUPPL. 2
, pp. 7
-
-
Luo, W.1
Rodina, A.2
Chiosis, G.3
-
44
-
-
34547183507
-
Roles of heat-shock protein 90 in maintaining and facilitating the neurodegenerative phenotype in tauopathies
-
DOI 10.1073/pnas.0701055104
-
Luo, W.; Dou, F.; Rodina, A.; Chip, S.; Kim, J.; Zhao, Q.; Moulick, K.; Aguirre, J.; Wu, N.; Greengard, P.; Chiosis, G. Roles of heat-shock protein 90 in maintaining and facilitating the neurodegenerative phenotype in tauopathies Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 9511-9516 (Pubitemid 47185810)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.22
, pp. 9511-9516
-
-
Luo, W.1
Dou, F.2
Rodina, A.3
Chip, S.4
Kim, J.5
Zhao, Q.6
Moulick, K.7
Aguirre, J.8
Wu, N.9
Greengard, P.10
Chiosis, G.11
-
45
-
-
33646246733
-
HSP induction mediates selective clearance of tau phosphorylated at proline-directed Ser/Thr sites but not KXGS (MARK) sites
-
DOI 10.1096/fj.05-5343fje
-
Dickey, C. A.; Dunmore, J.; Lu, B.; Wang, J.-W.; Lee, W. C.; Kamal, A.; Burrows, F.; Eckman, C.; Hutton, M.; Petrucelli, L. HSP induction mediates selective clearance of tau phosphorylated at proline-directed Ser/Thr sites but not KXGS (MARK) sites FASEB J. 2006, 20, 753-755 (Pubitemid 46671204)
-
(2006)
FASEB Journal
, vol.20
, Issue.6
, pp. 753-755
-
-
Dickey, C.A.1
Dunmore, J.2
Lu, B.3
Wang, J.-W.4
Lee, W.C.5
Kamal, A.6
Burrows, F.7
Eckman, C.8
Hutton, M.9
Petrucelli, L.10
-
46
-
-
20844450734
-
Development of a high throughput drug screening assay for the detection of changes in tau levels - Proof of concept with HSP90 inhibitors
-
DOI 10.2174/1567205053585927
-
Dickey, C. A.; Eriksen, J.; Kamal, A.; Burrows, F.; Kasibhatla, S.; Eckman, C. B.; Hutton, M.; Petrucelli, L. Development of a high throughput drug screening assay for the detection of changes in tau levels-proof of concept with HSP90 inhibitors Curr. Alzheimer Res. 2005, 2, 231-238 (Pubitemid 40862886)
-
(2005)
Current Alzheimer Research
, vol.2
, Issue.2
, pp. 231-238
-
-
Dickey, C.A.1
Eriksen, J.2
Kamal, A.3
Burrows, F.4
Kasibhatla, S.5
Eckman, C.B.6
Hutton, M.7
Petrucelli, L.8
-
47
-
-
78649767505
-
Hsp90 regulates tau pathology through co-chaperone complexes in Alzheimer's disease
-
Salminen, A.; Ojala, J.; Kaarniranta, K.; Hiltunen, M.; Soininen, H. Hsp90 regulates tau pathology through co-chaperone complexes in Alzheimer's disease Prog. Neurobiol. 2011, 93, 99-110
-
(2011)
Prog. Neurobiol.
, vol.93
, pp. 99-110
-
-
Salminen, A.1
Ojala, J.2
Kaarniranta, K.3
Hiltunen, M.4
Soininen, H.5
|