-
1
-
-
5044239107
-
Pathways of chaperone-mediated protein folding in the cytosol
-
Young JC, Agashe VR, Siegers K, Hartl FU, (2004) Pathways of chaperone-mediated protein folding in the cytosol. Nat Rev Mol Cell Biol 5: 781-791.
-
(2004)
Nat Rev Mol Cell Biol
, vol.5
, pp. 781-791
-
-
Young, J.C.1
Agashe, V.R.2
Siegers, K.3
Hartl, F.U.4
-
2
-
-
25844519550
-
HSP90 and the chaperoning of cancer
-
Whitesell L, Lindquist SL, (2005) HSP90 and the chaperoning of cancer. Nat Rev Cancer 5: 761-772.
-
(2005)
Nat Rev Cancer
, vol.5
, pp. 761-772
-
-
Whitesell, L.1
Lindquist, S.L.2
-
3
-
-
65549114190
-
Human 90 kDa Heat Shock Protein Hsp90 as a Target for Cancer Therapeutics
-
Lisandra MG, Ramos HIC, (2009) Human 90 kDa Heat Shock Protein Hsp90 as a Target for Cancer Therapeutics. Current Chemical Biology 3: 330-341.
-
(2009)
Current Chemical Biology
, vol.3
, pp. 330-341
-
-
Lisandra, M.G.1
Ramos, H.I.C.2
-
4
-
-
0035989680
-
HSP90 as a new therapeutic target for cancer therapy: the story unfolds
-
Maloney A, Workman P, (2002) HSP90 as a new therapeutic target for cancer therapy: the story unfolds. Expert Opin Biol Ther 2: 3-24.
-
(2002)
Expert Opin Biol Ther
, vol.2
, pp. 3-24
-
-
Maloney, A.1
Workman, P.2
-
5
-
-
0037315208
-
Regulation of signaling protein function and trafficking by the hsp90/hsp70-based chaperone machinery
-
Pratt WB, Toft DO, (2003) Regulation of signaling protein function and trafficking by the hsp90/hsp70-based chaperone machinery. Exp Biol Med (Maywood) 228: 111-133.
-
(2003)
Exp Biol Med (Maywood)
, vol.228
, pp. 111-133
-
-
Pratt, W.B.1
Toft, D.O.2
-
6
-
-
4744350064
-
Hsp90: the vulnerable chaperone
-
Chiosis G, Vilenchik M, Kim J, Solit D, (2004) Hsp90: the vulnerable chaperone. Drug Discov Today 9: 881-888.
-
(2004)
Drug Discov Today
, vol.9
, pp. 881-888
-
-
Chiosis, G.1
Vilenchik, M.2
Kim, J.3
Solit, D.4
-
7
-
-
55249109007
-
Recent advances in Hsp90 inhibitors as antitumor agents
-
Messaoudi S, Peyrat JF, Brion JD, Alami M, (2008) Recent advances in Hsp90 inhibitors as antitumor agents. Anticancer Agents Med Chem 8: 761-782.
-
(2008)
Anticancer Agents Med Chem
, vol.8
, pp. 761-782
-
-
Messaoudi, S.1
Peyrat, J.F.2
Brion, J.D.3
Alami, M.4
-
8
-
-
77950224150
-
Proposal for a role of the Hsp90/Hsp70-based chaperone machinery in making triage decisions when proteins undergo oxidative and toxic damage
-
Pratt WB, Morishima Y, Peng HM, Osawa Y, (2010) Proposal for a role of the Hsp90/Hsp70-based chaperone machinery in making triage decisions when proteins undergo oxidative and toxic damage. Exp Biol Med (Maywood) 235: 278-289.
-
(2010)
Exp Biol Med (Maywood)
, vol.235
, pp. 278-289
-
-
Pratt, W.B.1
Morishima, Y.2
Peng, H.M.3
Osawa, Y.4
-
9
-
-
0043288724
-
Heat shock protein 90 as a molecular target for cancer therapeutics
-
Isaacs JS, Xu W, Neckers L, (2003) Heat shock protein 90 as a molecular target for cancer therapeutics. Cancer Cell 3: 213-217.
-
(2003)
Cancer Cell
, vol.3
, pp. 213-217
-
-
Isaacs, J.S.1
Xu, W.2
Neckers, L.3
-
10
-
-
2642521990
-
Therapeutic and diagnostic implications of Hsp90 activation
-
Kamal A, Boehm MF, Burrows FJ, (2004) Therapeutic and diagnostic implications of Hsp90 activation. Trends Mol Med 10: 283-290.
-
(2004)
Trends Mol Med
, vol.10
, pp. 283-290
-
-
Kamal, A.1
Boehm, M.F.2
Burrows, F.J.3
-
11
-
-
84866309629
-
EC144 is a potent inhibitor of the heat shock protein 90
-
Shi J, Van de Water R, Hong K, Lamer RB, Weichert KW, et al. (2012) EC144 is a potent inhibitor of the heat shock protein 90. J Med Chem 55: 7786-7795.
-
(2012)
J Med Chem
, vol.55
, pp. 7786-7795
-
-
Shi, J.1
Van de Water, R.2
Hong, K.3
Lamer, R.B.4
Weichert, K.W.5
-
12
-
-
0141484615
-
A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
-
Kamal A, Thao L, Sensintaffar J, Zhang L, Boehm MF, et al. (2003) A high-affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors. Nature 425: 407-410.
-
(2003)
Nature
, vol.425
, pp. 407-410
-
-
Kamal, A.1
Thao, L.2
Sensintaffar, J.3
Zhang, L.4
Boehm, M.F.5
-
13
-
-
1142273472
-
Altered states: selectively drugging the Hsp90 cancer chaperone
-
Workman P, (2004) Altered states: selectively drugging the Hsp90 cancer chaperone. Trends Mol Med 10: 47-51.
-
(2004)
Trends Mol Med
, vol.10
, pp. 47-51
-
-
Workman, P.1
-
14
-
-
0029123128
-
erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships
-
Schnur RC, Corman ML, Gallaschun RJ, Cooper BA, Dee MF, et al. (1995) erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships. J Med Chem 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
-
15
-
-
26444462561
-
Preclinical toxicity of a geldanamycin analog, 17-(dimethylaminoethylamino)-17-demethoxygeldanamycin (17-DMAG), in rats and dogs: potential clinical relevance
-
Glaze E, Lambert A, Smith A, Page J, Johnson W, et al. (2005) Preclinical toxicity of a geldanamycin analog, 17-(dimethylaminoethylamino)-17-demethoxygeldanamycin (17-DMAG), in rats and dogs: potential clinical relevance. Cancer Chemotherapy and Pharmacology 56: 637-647.
-
(2005)
Cancer Chemotherapy and Pharmacology
, vol.56
, pp. 637-647
-
-
Glaze, E.1
Lambert, A.2
Smith, A.3
Page, J.4
Johnson, W.5
-
16
-
-
33746662241
-
Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90
-
Ge J, Normant E, Porter JR, Ali JA, Dembski MS, et al. (2006) Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. J Med Chem 49: 4606-4615.
-
(2006)
J Med Chem
, vol.49
, pp. 4606-4615
-
-
Ge, J.1
Normant, E.2
Porter, J.R.3
Ali, J.A.4
Dembski, M.S.5
-
17
-
-
59449108495
-
A phase II trial of 17-allylamino-17-demethoxygeldanamycin in patients with hormone-refractory metastatic prostate cancer
-
Heath EI, Hillman DW, Vaishampayan U, Sheng S, Sarkar F, et al. (2008) A phase II trial of 17-allylamino-17-demethoxygeldanamycin in patients with hormone-refractory metastatic prostate cancer. Clin Cancer Res 14: 7940-7946.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 7940-7946
-
-
Heath, E.I.1
Hillman, D.W.2
Vaishampayan, U.3
Sheng, S.4
Sarkar, F.5
-
18
-
-
58149340657
-
Phase II trial of 17-allylamino-17-demethoxygeldanamycin in patients with metastatic melanoma
-
Solit DB, Osman I, Polsky D, Panageas KS, Daud A, et al. (2008) Phase II trial of 17-allylamino-17-demethoxygeldanamycin in patients with metastatic melanoma. Clin Cancer Res 14: 8302-8307.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 8302-8307
-
-
Solit, D.B.1
Osman, I.2
Polsky, D.3
Panageas, K.S.4
Daud, A.5
-
19
-
-
58149180924
-
A phase 1 dose-escalation study of irinotecan in combination with 17-allylamino-17-demethoxygeldanamycin in patients with solid tumors
-
Tse AN, Klimstra DS, Gonen M, Shah M, Sheikh T, et al. (2008) A phase 1 dose-escalation study of irinotecan in combination with 17-allylamino-17-demethoxygeldanamycin in patients with solid tumors. Clin Cancer Res 14: 6704-6711.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 6704-6711
-
-
Tse, A.N.1
Klimstra, D.S.2
Gonen, M.3
Shah, M.4
Sheikh, T.5
-
20
-
-
51449093764
-
Targeting Hsp90: small-molecule inhibitors and their clinical development
-
Taldone T, Gozman A, Maharaj R, Chiosis G, (2008) Targeting Hsp90: small-molecule inhibitors and their clinical development. Curr Opin Pharmacol 8: 370-374.
-
(2008)
Curr Opin Pharmacol
, vol.8
, pp. 370-374
-
-
Taldone, T.1
Gozman, A.2
Maharaj, R.3
Chiosis, G.4
-
21
-
-
58849160500
-
Heat shock protein 90 as a drug target: some like it hot
-
Banerji U, (2009) Heat shock protein 90 as a drug target: some like it hot. Clin Cancer Res 15: 9-14.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 9-14
-
-
Banerji, U.1
-
22
-
-
41149111451
-
The Hsp90 molecular chaperone: an open and shut case for treatment
-
Pearl LH, Prodromou C, Workman P, (2008) The Hsp90 molecular chaperone: an open and shut case for treatment. Biochem J 410: 439-453.
-
(2008)
Biochem J
, vol.410
, pp. 439-453
-
-
Pearl, L.H.1
Prodromou, C.2
Workman, P.3
-
23
-
-
38349157746
-
4,5-diarylisoxazole Hsp90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer
-
Brough PA, Aherne W, Barril X, Borgognoni J, Boxall K, et al. (2008) 4,5-diarylisoxazole Hsp90 chaperone inhibitors: potential therapeutic agents for the treatment of cancer. J Med Chem 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
-
24
-
-
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
-
Eiseman JL, Lan J, Lagattuta TF, Hamburger DR, Joseph E, et al. (2005) 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 Chemotherapy and Pharmacology 55: 21-32.
-
(2005)
Cancer Chemotherapy and Pharmacology
, vol.55
, pp. 21-32
-
-
Eiseman, J.L.1
Lan, J.2
Lagattuta, T.F.3
Hamburger, D.R.4
Joseph, E.5
-
25
-
-
84866865006
-
Pharmacophore-based virtual screening and biological evaluation of small molecule inhibitors for protein arginine methylation
-
Wang J, Chen L, Sinha SH, Liang Z, Chai H, et al. (2012) Pharmacophore-based virtual screening and biological evaluation of small molecule inhibitors for protein arginine methylation. J Med Chem 55: 7978-7987.
-
(2012)
J Med Chem
, vol.55
, pp. 7978-7987
-
-
Wang, J.1
Chen, L.2
Sinha, S.H.3
Liang, Z.4
Chai, H.5
-
26
-
-
84867804995
-
Design, Synthesis, and Structure-Activity Relationships of Highly Potent 5-HT(3) Receptor Ligands
-
Verheij MH, Thompson AJ, van Muijlwijk-Koezen JE, Lummis SC, Leurs R, et al. (2012) Design, Synthesis, and Structure-Activity Relationships of Highly Potent 5-HT(3) Receptor Ligands. J Med Chem 55: 8603-8614.
-
(2012)
J Med Chem
, vol.55
, pp. 8603-8614
-
-
Verheij, M.H.1
Thompson, A.J.2
van Muijlwijk-Koezen, J.E.3
Lummis, S.C.4
Leurs, R.5
-
27
-
-
84861517739
-
On the value of homology models for virtual screening: discovering hCXCR3 antagonists by pharmacophore-based and structure-based approaches
-
Huang D, Gu Q, Ge H, Ye J, Salam NK, et al. (2012) On the value of homology models for virtual screening: discovering hCXCR3 antagonists by pharmacophore-based and structure-based approaches. J Chem Inf Model 52: 1356-1366.
-
(2012)
J Chem Inf Model
, vol.52
, pp. 1356-1366
-
-
Huang, D.1
Gu, Q.2
Ge, H.3
Ye, J.4
Salam, N.K.5
-
28
-
-
40649097784
-
Identification of ligand features essential for HDACs inhibitors by pharmacophore modeling
-
Chen YD, Jiang YJ, Zhou JW, Yu QS, You QD, (2008) Identification of ligand features essential for HDACs inhibitors by pharmacophore modeling. J Mol Graph Model 26: 1160-1168.
-
(2008)
J Mol Graph Model
, vol.26
, pp. 1160-1168
-
-
Chen, Y.D.1
Jiang, Y.J.2
Zhou, J.W.3
Yu, Q.S.4
You, Q.D.5
-
29
-
-
68549115383
-
Combining hit identification strategies: fragment-based and in silico approaches to orally active 2-aminothieno[2,3-d]pyrimidine inhibitors of the Hsp90 molecular chaperone
-
Brough PA, Barril X, Borgognoni J, Chene P, Davies NG, et al. (2009) Combining hit identification strategies: fragment-based and in silico approaches to orally active 2-aminothieno[2,3-d]pyrimidine inhibitors of the Hsp90 molecular chaperone. J Med Chem 52: 4794-4809.
-
(2009)
J Med Chem
, vol.52
, pp. 4794-4809
-
-
Brough, P.A.1
Barril, X.2
Borgognoni, J.3
Chene, P.4
Davies, N.G.5
-
30
-
-
26844468809
-
3-(5-Chloro-2,4-dihydroxyphenyl)-pyrazole-4-carboxamides as inhibitors of the Hsp90 molecular chaperone
-
Brough PA, Barril X, Beswick M, Dymock BW, Drysdale MJ, et al. (2005) 3-(5-Chloro-2,4-dihydroxyphenyl)-pyrazole-4-carboxamides as inhibitors of the Hsp90 molecular chaperone. Bioorg Med Chem Lett 15: 5197-5201.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 5197-5201
-
-
Brough, P.A.1
Barril, X.2
Beswick, M.3
Dymock, B.W.4
Drysdale, M.J.5
-
31
-
-
72949097266
-
Improving virtual screening performance against conformational variations of receptors by shape matching with ligand binding pocket
-
Lee HS, Lee CS, Kim JS, Kim DH, Choe H, (2009) Improving virtual screening performance against conformational variations of receptors by shape matching with ligand binding pocket. J Chem Inf Model 49: 2419-2428.
-
(2009)
J Chem Inf Model
, vol.49
, pp. 2419-2428
-
-
Lee, H.S.1
Lee, C.S.2
Kim, J.S.3
Kim, D.H.4
Choe, H.5
-
32
-
-
0031552362
-
Development and validation of a genetic algorithm for flexible docking
-
Jones G, Willett P, Glen RC, Leach AR, Taylor R, (1997) Development and validation of a genetic algorithm for flexible docking. J Mol Biol 267: 727-748.
-
(1997)
J Mol Biol
, vol.267
, pp. 727-748
-
-
Jones, G.1
Willett, P.2
Glen, R.C.3
Leach, A.R.4
Taylor, R.5
-
33
-
-
0028273420
-
Characterization and kinetic analysis of the intracellular domain of human protein tyrosine phosphatase beta (HPTP beta) using synthetic phosphopeptides
-
Harder KW, Owen P, Wong LK, Aebersold R, Clark-Lewis I, et al. (1994) Characterization and kinetic analysis of the intracellular domain of human protein tyrosine phosphatase beta (HPTP beta) using synthetic phosphopeptides. Biochem J 298 (Pt 2): 395-401.
-
(1994)
Biochem J
, vol.298
, Issue.Pt 2
, pp. 395-401
-
-
Harder, K.W.1
Owen, P.2
Wong, L.K.3
Aebersold, R.4
Clark-Lewis, I.5
-
34
-
-
0034654395
-
A sensitive assay for phosphoinositide phosphatases
-
Maehama T, Taylor GS, Slama JT, Dixon JE, (2000) A sensitive assay for phosphoinositide phosphatases. Anal Biochem 279: 248-250.
-
(2000)
Anal Biochem
, vol.279
, pp. 248-250
-
-
Maehama, T.1
Taylor, G.S.2
Slama, J.T.3
Dixon, J.E.4
-
36
-
-
77958516062
-
ATPases as Drug Targets: Insights from Heat Shock Proteins 70 and 90
-
Massey AJ, (2010) ATPases as Drug Targets: Insights from Heat Shock Proteins 70 and 90. Journal of Medicinal Chemistry 53: 7280-7286.
-
(2010)
Journal of Medicinal Chemistry
, vol.53
, pp. 7280-7286
-
-
Massey, A.J.1
|