-
1
-
-
0027246046
-
Synthesis and cytotoxicity of l,6,7,8-substituted-2-(4'-substituted phenyl)-4-quin.olones and related, compounds: Identification as antimitotic agents interacting with tubulin
-
Kuo, S. G; Lee, H. Z.; Juang, J. P.; Lin, Y. T.; Wu, T. S.; Chang, J. J.; Lednicer, D.; Paull, K. D.; Lin, C. M. Synthesis and cytotoxicity of l,6,7,8-substituted-2-(4'-substituted phenyl)-4-quin.olones and related, compounds: identification as antimitotic agents interacting with tubulin. J Med. Chem. 1993, 36(9), 1146-1156.
-
(1993)
J. Med. Chem.
, vol.36
, Issue.9
, pp. 1146-1156
-
-
Kuo, S.G.1
Lee, H.Z.2
Juang, J.P.3
Lin, Y.T.4
Wu, T.S.5
Chang, J.J.6
Lednicer, D.7
Paull, K.D.8
Lin, C.M.9
-
2
-
-
0028295948
-
Antitumor agents. 150. 2′,3′,4′,5′,5,6, 7Substituted 2-ph.enyl-4-quinolones and related compounds: Their synthesis, cytotoxicity, and inhibition of tubulin, polymerization
-
Li, L.; Wang, H. K.; Kuo, S. C.; Wu, T. S.; Lednicer, D.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 150. 2′,3′,4′, 5′,5,6,7Substituted 2-ph.enyl-4-quinolones and related compounds: their synthesis, cytotoxicity, and inhibition of tubulin, polymerization. J. Med. Chem- 1994,37(8), 1126-1135.
-
(1994)
J. Med. Chem.
, vol.37
, Issue.8
, pp. 1126-1135
-
-
Li, L.1
Wang, H.K.2
Kuo, S.C.3
Wu, T.S.4
Lednicer, D.5
Lin, C.M.6
Hamel, E.7
Lee, K.H.8
-
3
-
-
0028036429
-
Antitumor agents 155. Synthesis and biological evaluation of 3',6,7- Substituted 2-phenyl-4-quinolones as antimicrotubule agents
-
DOI 10.1021/jm00046a025
-
Li, L.; Wang, H. K.; Kuo, S. C.; Wu, T. S.; Mauger, A.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 155. Synthesis and biological evaluation of 3',6,7-substituted 2-phenyl-4-quinolones as antimicrotubule agents. J. Med. Chem. 1994,37 (20), 3400-3407. (Pubitemid 24325054)
-
(1994)
Journal of Medicinal Chemistry
, vol.37
, Issue.20
, pp. 3400-3407
-
-
Li, L.1
Wang, H.-K.2
Kuo, S.-C.3
Wu, T.-S.4
Mauger, A.5
Lin, C.M.6
Hamel, E.7
Lee, K.-H.8
-
4
-
-
0030738726
-
Antitumor agents. 174. 2′,3′,4′,5,6,7-Substituted 2phenyl-1,8-naph.thyridin-4-ones their synthesis, cytotoxicity, and inhibition of tubulin polymerization
-
Chen, K.; Kuo, S. C.; Hsieh, M. C.; Mauger, A.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 174. 2′,3′,4′,5,6,7-Substituted 2phenyl-1,8-naph.thyridin-4-ones their synthesis, cytotoxicity, and inhibition of tubulin polymerization. J. Med. Chem-1997,40 (14), 2266-2275.
-
(1997)
J. Med. Chem.
, vol.40
, Issue.14
, pp. 2266-2275
-
-
Chen, K.1
Kuo, S.C.2
Hsieh, M.C.3
Mauger, A.4
Lin, C.M.5
Hamel, E.6
Lee, K.H.7
-
5
-
-
0030823308
-
Antitumor agents. 178. Synthesis and biological, evaluation of substituted 2-aryl-l,8-naphthyridin-4(lH)-ones as antitumor agents that inhibit tubulin polymerization
-
Chen, K.; Kuo, S. C.; Hsieh, M. C.; Mauger, A.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 178. Synthesis and biological, evaluation of substituted 2-aryl-l,8-naphthyridin-4(lH)-ones as antitumor agents that inhibit tubulin polymerization. J. Med. Chem. 1997, 40 (19), 3049-3056.
-
(1997)
J. Med. Chem.
, vol.40
, Issue.19
, pp. 3049-3056
-
-
Chen, K.1
Kuo, S.C.2
Hsieh, M.C.3
Mauger, A.4
Lin, C.M.5
Hamel, E.6
Lee, K.H.7
-
6
-
-
0032568390
-
Antitumor agents. 181. Synthesis and biological evaluation of 6,7,2′,3′,4′-substitutedl,2,3,4-tetrahydro-2-phenyl-4- quinolones as a new class of antimitotic antitumor agents
-
Xia, Y.; Yang, Z. Y.; Xia, P.; Bastow, K. F.; Tachibana, Y.; Kuo, S. C.; Hamel, E.; Hackl, T.; Lee, K. H. Antitumor agents. 181. Synthesis and biological evaluation of 6,7,2′,3′,4′-substitutedl,2,3,4-tetrahydro-2- phenyl-4-quinolones as a new class of antimitotic antitumor agents. J. Med. Chem. 1998, 41 (7), 1155-1162.
-
(1998)
J. Med. Chem.
, vol.41
, Issue.7
, pp. 1155-1162
-
-
Xia, Y.1
Yang, Z.Y.2
Xia, P.3
Bastow, K.F.4
Tachibana, Y.5
Kuo, S.C.6
Hamel, E.7
Hackl, T.8
Lee, K.H.9
-
7
-
-
0033533865
-
Antitumor agents. 196. Substituted 2-thienyl-l,8-naphthyridin-4-ones: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization
-
Zhang, S. X.; Bastow, K. F.; Tachibana, Y.; Kuo, S. C.; Hamel, E.; Mauger, A.; Narayanan, V. L.; Lee, K. H. Antitumor agents. .196. Substituted 2-thienyl-l,8-naphthyridin-4-ones: their synthesis, cytotoxicity, and inhibition of tubulin polymerization. J. Med. Chem. 1999, 42 (20), 4081-4087.
-
(1999)
J. Med. Chem.
, vol.42
, Issue.20
, pp. 4081-4087
-
-
Zhang, S.X.1
Bastow, K.F.2
Tachibana, Y.3
Kuo, S.C.4
Hamel, E.5
Mauger, A.6
Narayanan, V.L.7
Lee, K.H.8
-
8
-
-
0034719321
-
Antitumor agents. 199. Three-dimensional quantitative structure-activity relationship study of the colchicines binding site ligands using comparative molecular field analysis
-
Zhang, S. X.; Feng, J.; Kuo, S. C.; Brossi, A.; Hamel, E.; Tropsha, A.; Lee, K. H. Antitumor agents. 199. Three-dimensional quantitative structure-activity relationship study of the colchicines binding site ligands using comparative molecular field analysis. J. Med. Chem- 2000, 43 (2), 167-176.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.2
, pp. 167-176
-
-
Zhang, S.X.1
Feng, J.2
Kuo, S.C.3
Brossi, A.4
Hamel, E.5
Tropsha, A.6
Lee, K.H.7
-
9
-
-
0034676319
-
6-Alkylamino- And 2,3dihydro-3′-methoxy-2-phenyl-4-quinazolinones and related, compounds: Their synthesis, cytotoxicty, and inhibition, of tubulin polymerization
-
Hour, M. J.; Huang, L. J.; Kuo, S. C.; Xia, Y.; Bastow, K.; Nakanishi, Y.; Hamel, E.; Lee, K. H. 6-Alkylamino- and 2,3dihydro-3′-methoxy-2- phenyl-4-quinazolinones and related, compounds: their synthesis, cytotoxicty, and inhibition, of tubulin polymerization. J. Med. Chem- 2000, 43 (23), 4479-4487.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.23
, pp. 4479-4487
-
-
Hour, M.J.1
Huang, L.J.2
Kuo, S.C.3
Xia, Y.4
Bastow, K.5
Nakanishi, Y.6
Hamel, E.7
Lee, K.H.8
-
10
-
-
0035829462
-
Antitumor agents. 211. Fluorina ted 2-phenyl4-quinolone derivatives as antimitotic antitumor agents
-
Xia, Y.; Yang, Z. Y.; Xia, P.; Hackl, T.; Hamel, E.; Mauger, A.; Wu, J. H.; Lee, K. H. Antitumor agents. 211. Fluorina ted 2-phenyl4-quinolone derivatives as antimitotic antitumor agents. J. Med. Chem. 2001, 44 (23), 3932-3936.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.23
, pp. 3932-3936
-
-
Xia, Y.1
Yang, Z.Y.2
Xia, P.3
Hackl, T.4
Hamel, E.5
Mauger, A.6
Wu, J.H.7
Lee, K.H.8
-
11
-
-
0035821397
-
Antitumor agents. Part 204: Synthesis and biological evaluation of substituted 2-aryl quinazolinones
-
Xia, T.; Yang, Z. Y.; Hour, M. J.; Kuo, S. C.; Xia, P.; Bastow, K. F.; Nakanishi, Y.; Nampoothiri, P.; Hackl, T.; Hamel, E.; Lee, K. H. Antitumor agents. Part 204: Synthesis and biological evaluation of substituted 2-aryl quinazolinones. Bioorg. Med. Chem. Lett2001, 11(9), 1193-1196.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.9
, pp. 1193-1196
-
-
Xia, T.1
Yang, Z.Y.2
Hour, M.J.3
Kuo, S.C.4
Xia, P.5
Bastow, K.F.6
Nakanishi, Y.7
Nampoothiri, P.8
Hackl, T.9
Hamel, E.10
Lee, K.H.11
-
12
-
-
0242493914
-
Antitumor agents. Part 226: Synthesis and cytotoxicity of 2-phenyl-4-quinolone acetic acids and their esters
-
Xia, T.; Yang, Z. Y.; Xia, P.; Bastow, K. F.; Nakanishi, Y.; Nampoothiri, P.; Hamel, E.; Brossi, A.; Lee, K. H. Antitumor agents. Part 226: Synthesis and cytotoxicity of 2-phenyl-4-quinolone acetic acids and their esters. Bioorg. Med Chem. Lett. 2003, 13 (17), 2891-2893.
-
(2003)
Bioorg. Med Chem. Lett.
, vol.13
, Issue.17
, pp. 2891-2893
-
-
Xia, T.1
Yang, Z.Y.2
Xia, P.3
Bastow, K.F.4
Nakanishi, Y.5
Nampoothiri, P.6
Hamel, E.7
Brossi, A.8
Lee, K.H.9
-
13
-
-
9644266706
-
Synthesis and biological relationships of 3′,6-substituted 2-phenyl-4-quinolone-3-carboxylic acid, derivatives as antimitotic agents
-
Lai, Y. Y.; Huang, L. J.; Lee, K. H.; Xiao, Z. Y.; Bastow, K. F.; Yamori, T.; Kuo, S. C. Synthesis and biological relationships of 3′,6-substituted 2-phenyl-4-quinolone-3-carboxylic acid, derivatives as antimitotic agents. Bioorg. Med. Chem. 2005,13 (1), 265-275.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, Issue.1
, pp. 265-275
-
-
Lai, Y.Y.1
Huang, L.J.2
Lee, K.H.3
Xiao, Z.Y.4
Bastow, K.F.5
Yamori, T.6
Kuo, S.C.7
-
14
-
-
20444459868
-
Cancer preventive agents, Part 2: Synthesis and evaluation of 2-phenyl-4-quinolone and 9-oxo-9,10-dihydroacridine derivatives as novel antitumor promoters
-
Nakamura, S; Kozuka, M.; Bastow, K. F.; Tokuda, H.; Nishino, H.; Suzuki, M.; Tatsuzaki, J.; Morris-Natschke, S. L.; Kuo, S. C.; Lee, K. H. Cancer preventive agents, Part 2: Synthesis and evaluation of 2-phenyl-4-quinolone and 9-oxo-9,10-dihydroacridine derivatives as novel antitumor promoters. Bioorg. Med. Chem. 2005, 13 (14), 4396-4401.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, Issue.14
, pp. 4396-4401
-
-
Nakamura, S.1
Kozuka, M.2
Bastow, K.F.3
Tokuda, H.4
Nishino, H.5
Suzuki, M.6
Tatsuzaki, J.7
Morris-Natschke, S.L.8
Kuo, S.C.9
Lee, K.H.10
-
15
-
-
39749168393
-
CHM-I, a novel synthetic quinolone with potent and selective antimitotic antitumor activity against human hepatocellular carcinoma in vitro and in. vivo
-
Wang, S. W.; Pan. S. L.; Huang, Y. C.; Guh. J. H.; Chiang, P. C,; Huang, D. Y; Kuo, S. C.; Lee, K. H.; Teng, C. M. CHM-I, a novel synthetic quinolone with potent and selective antimitotic antitumor activity against human hepatocellular carcinoma in vitro and in. vivo. Mol. Cancer Ther. 2008, 7 (2), 350-360.
-
(2008)
Mol. Cancer Ther.
, vol.7
, Issue.2
, pp. 350-360
-
-
Wang, S.W.1
Pan, S.L.2
Huang, Y.C.3
Guh, J.H.4
Chiang, P.C.5
Huang, D.Y.6
Kuo, S.C.7
Lee, K.H.8
Teng, C.M.9
-
16
-
-
0038692005
-
Absorption rate limit considerations for oral phosphate prodrugs
-
DOI 10.1023/A:1023827017224
-
Heimbach, T; Oh, D. M.; Li, L. Y.; Forsberg, M.; Savolainen, J.; Leppänen, J.; Matsunaga, Y.; Flynn, G.; Fleisher, D. Absorption rate limit considerations for oral phosphate prodrug. Pharm. Res. 2003, 20 (6), 848-856. (Pubitemid 36628429)
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.6
, pp. 848-856
-
-
Heimbach, T.1
Oh, D.-M.2
Li, L.Y.3
Forsberg, M.4
Savolainen, J.5
Leppanen, J.6
Matsunaga, Y.7
Flynn, G.8
Fleisher, D.9
-
17
-
-
0036083301
-
Mechanisms of action of antitumor drugs that interact with microtubules and tubulin
-
Jordan, M. A. Mechanisms of action of antitumor drugs that interact with microtubules and tubulin. Curr. Med. Chem. Antitansir Agents 2002, 2, 1-17.
-
(2002)
Curr. Med. Chem. Antitansir Agents
, vol.2
, pp. 1-17
-
-
Jordan, M.A.1
-
18
-
-
0024801479
-
Cardiovascular and renal action of dopaminergic prodrugs
-
Casagrande, C.; Merlo, L.; Ferrini, R.; Miragoli, G.; Semeraro, C. Cardiovascular and renal action of dopaminergic prodrugs. J., Cardiovas, Pharmacol-1989, 14, S40-S59.
-
(1989)
J. Cardiovas Pharmacol
, vol.14
-
-
Casagrande, C.1
Merlo, L.2
Ferrini, R.3
Miragoli, G.4
Semeraro, C.5
-
19
-
-
0037406988
-
Anandamide prodrugs: 1. Water-soluble phosphate esters of arachidonylethanolamide and R-methanandamide
-
DOI 10.1016/S0928-0987(03)00044-7
-
Juntunen, J.; Huuskonen, J.; Laine, K.; Niemi, R.; Taipale, H.; Nevalainen, T.; Pate, D. W.; Järvinen, T. Anandamide prodrugs 1. Water-soluble phosphate esters of arachidonylethanolamide and. R-methanandamid.e. Eur, J, Pharm, Sci. 2003, 19 (1), 37-43. (Pubitemid 36506936)
-
(2003)
European Journal of Pharmaceutical Sciences
, vol.19
, Issue.1
, pp. 37-43
-
-
Juntunen, J.1
Huuskonen, J.2
Laine, K.3
Niemi, R.4
Taipale, H.5
Nevalainen, T.6
Pate, D.W.7
Jarvinen, T.8
-
20
-
-
0037030688
-
Antineoplastic agents. 465. Structural modification of resveratrol: Sodium, resverastatin phosphate
-
Pettit, G. R.; Grealish, M. P.; Jung, M. K.; Hamel, E.; Pettit, R. K.; Chapuis, J. C.; Schmidt, J. M. Antineoplastic agents. 465. Structural modification of resveratrol: sodium, resverastatin phosphate. J. Med. Chem- 2002, 45 (12), 2534-2542.
-
(2002)
J. Med. Chem.
, vol.45
, Issue.12
, pp. 2534-2542
-
-
Pettit, G.R.1
Grealish, M.P.2
Jung, M.K.3
Hamel, E.4
Pettit, R.K.5
Chapuis, J.C.6
Schmidt, J.M.7
-
21
-
-
0029338274
-
Estramustine phosphate sodium. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in prostate cancer
-
Perry, C. M.; McTavish, D. Estramustine phosphate sodium. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in prostate cancer. Drugs Aging 1995, 7(1), 49-74.
-
(1995)
Drugs Aging
, vol.7
, Issue.1
, pp. 49-74
-
-
Perry, C.M.1
McTavish, D.2
-
22
-
-
0029856304
-
Etoposide phosphate, the water soluble prodrug of etoposide
-
DOI 10.1007/BF00820727
-
Witterland, A. H. I.; Koks, C. H. W.; Beijnen, J. H. Etoposide phosphate, the water soluble prodrug of etoposide. Pharm. World Sci- 1996, 18, 163-170. (Pubitemid 26364524)
-
(1996)
Pharmacy World and Science
, vol.18
, Issue.5
, pp. 163-170
-
-
Witterland, A.H.I.1
Koks, C.H.W.2
Beijnen, J.H.3
-
23
-
-
27644466314
-
Combretastatin A4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-cadherin signaling
-
DOI 10.1172/JCI24586
-
Vincent, L.; Kermani, P.; Young, L. M.; Cheng, J.; Fan, Z.; Shido, K.; Lam, G.; Bompais-Vincent, H.; Zhu, Z.; Hicklin, D. J.; Bohlen, P.; Chaplin, D. J.; May, C.; Rafii, S. Combretastatin A4 phosphate induces rapid regression of tumor neovessels and growth through interference with, vascular endothelial-cadherin signaling. J. Clin. Invest. 2005, 115 (11), 2992-3006. (Pubitemid 41567565)
-
(2005)
Journal of Clinical Investigation
, vol.115
, Issue.11
, pp. 2992-3006
-
-
Vincent, L.1
Kermani, P.2
Young, L.M.3
Cheng, J.4
Zhang, F.5
Shido, K.6
Lam, G.7
Bompais-Vincent, H.8
Zhu, Z.9
Hicklin, D.J.10
Bohlen, P.11
Chaplin, D.J.12
May, C.13
Rafii, S.14
-
24
-
-
0029044610
-
Antineoplastic agents 322. Synthesis of combretastatin A-4 prodrugs
-
Pettit, G. R.; Temple, C.; Narayanan, V. L.; Varma, R.; Simpson, M. J.; Boyd, M. R.; Rener, G. A.; Bansal, N. Antineoplastic agents 322. Synthesis of combretastatin A-4 prodrugs. Anti-Cancer Drug Des. 1995, 10 (4), 299-309.
-
(1995)
Anti-Cancer Drug Des.
, vol.10
, Issue.4
, pp. 299-309
-
-
Pettit, G.R.1
Temple, C.2
Narayanan, V.L.3
Varma, R.4
Simpson, M.J.5
Boyd, M.R.6
Rener, G.A.7
Bansal, N.8
-
25
-
-
37349119362
-
Synthesis and in vivo antitumor evaluation of 2-methoxyestradiol 3-phosphate, 17-phosphate, and 3,17-diphosphate
-
Edsall, A.; Agoston, G.; Treston, A.; Plum, S.; McClanahan, R.; Lu, T.; Song, W.; Cushman, M. Synthesis and in vivo antitumor evaluation of 2-methoxyestradiol 3-phosphate, 17-phosphate, and 3,17-diphosphate. J. Med. Chem- 2007, 50 (26), 6700-6705.
-
(2007)
J. Med. Chem.
, vol.50
, Issue.26
, pp. 6700-6705
-
-
Edsall, A.1
Agoston, G.2
Treston, A.3
Plum, S.4
McClanahan, R.5
Lu, T.6
Song, W.7
Cushman, M.8
-
26
-
-
0036009653
-
Synthesis and biologic evaluation, of a radioiodinated quinazolinone derivative for enzyme-mediated insolubilization therapy
-
Ho, N. H.; Harapanhalli, R. S.; Dahman, B. A.; Chen, K.; Wang, K.; Adelstein, S. J.; Kassis, A. I. Synthesis and biologic evaluation, of a radioiodinated quinazolinone derivative for enzyme-mediated insolubilization therapy. Bioconiugate Chem- 2002, 13 (2), 357-364.
-
(2002)
Bioconiugate Chem.
, vol.13
, Issue.2
, pp. 357-364
-
-
Ho, N.H.1
Harapanhalli, R.S.2
Dahman, B.A.3
Chen, K.4
Wang, K.5
Adelstein, S.J.6
Kassis, A.I.7
-
27
-
-
33846226440
-
Silico design, synthesis, and biological evaluation of radioiodinated quinazolinone derivatives for alkaline phosphatase-mediated cancer diagnosis and therapy
-
DOI 10.1158/1535-7163.MCT-06-0465
-
Chen, K.; Wang, K; Kirichian, A.M.; Al Aowad, A. F.; Iyer, L. K.; Adelstein, S. J.; Kassis, A. I. In silico design, synthesis, and biological evaluation of radioiodinated quinazolinone derivatives for alkaline phosphatase-mediated cancer diagnosis and therapy. Mol. Cancer Ther- 2006, 5 (12), 3001-3013. (Pubitemid 46092041)
-
(2006)
Molecular Cancer Therapeutics
, vol.5
, Issue.12
, pp. 3001-3013
-
-
Chen, K.1
Wang, K.2
Kirichian, A.M.3
Al Aowad, A.F.4
Iyer, L.K.5
Adelstein, S.J.6
Kassis, A.I.7
-
28
-
-
33947236862
-
Computational modeling and experimental evaluation of a novel prodrug for targeting the extracellular space of prostate tumors
-
DOI 10.1158/0008-5472.CAN-06-3309
-
Posoisil, P.; Wang, K.; Al Aowad, A. F.; Iyer, L. K.; Adelstein, S. J.; Kassis, A. I. Computational modeling and experimental evaluation of a novel prodrug for targeting the extracellular space of prostate tumors. Cancer Res. 2007, 67, 2197-2205. (Pubitemid 46424239)
-
(2007)
Cancer Research
, vol.67
, Issue.5
, pp. 2197-2205
-
-
Pospisil, P.1
Wang, K.2
Al Aowad, A.F.3
Iyer, L.K.4
Adelstein, S.J.5
Kassis, A.I.6
-
29
-
-
33947264285
-
Evaluation of chemical, physical, and biologic properties of tumor-targeting radioiodinated quinazolinone derivative
-
DOI 10.1021/bc0602937
-
Wang, K.; Kirichian, A. M.; Al Aowad, A. F.; Adelstein, S. J.; Kassis, A. I. Evaluation of chemical, physical, and biologic properties of tumor-targeting radioiodinated quinazolinone derivative. Bioconiuzate Chem. 2007, 18, 754-764. (Pubitemid 47010795)
-
(2007)
Bioconjugate Chemistry
, vol.18
, Issue.3
, pp. 754-764
-
-
Wang, K.1
Kirichian, A.M.2
Al Aowad, A.F.3
Adelstein, S.J.4
Kassis, A.I.5
-
30
-
-
37049160414
-
Hydroxypyridine and hydroxyquinoline phosphates as anticholinesterases
-
Andrews, K. J. M.; Atherton, F. R.; Bergel, F.; Morrison, A. L. Hydroxypyridine and hydroxyquinoline phosphates as anticholinesterases. J., Chem. Soc. 1954, 1638-1640.
-
(1954)
J. Chem. Soc.
, pp. 1638-1640
-
-
Andrews, K.J.M.1
Atherton, F.R.2
Bergel, F.3
Morrison, A.L.4
-
31
-
-
0020425546
-
New 4-quinolinoland 5,6,7,8-tetrahydro-4-quinolinol derivatives with biocidal effect
-
Horst, G.; Harald, K.; Hilmar, M.; Gerhard, S. New 4-quinolinoland 5,6,7,8-tetrahydro-4-quinolinol derivatives with biocidal effect. Liebigs Ann. Chem. 1982, 1656-1676.
-
(1982)
Liebigs Ann. Chem.
, pp. 1656-1676
-
-
Horst, G.1
Harald, K.2
Hilmar, M.3
Gerhard, S.4
-
32
-
-
0033566690
-
Potent antitumor activity of MS-247, a novel DNA minor groove binder, evaluated by an in vitro and in vivo human cancer cell line panel
-
Yamori, T.; Matsunaga, A.; Sato, S.; Yamazaki, K.; Komi, A.; Ishizu, K.; Mita, I.; Edatsugi, H.; Matsuba, Y.; Takezawaj K.; Nakanishi, O.; Kohno, H.; Nakajima, Y.; Komatsu, H.; Andoh, T.; Tsuruo, T. Potent antitumor activity of MS-247, a novel DNA minor groove binder, evaluated by an in vitro and in vivo human cancer cell line panel. Cancer Res. 1999, 59, 4042-4049. (Pubitemid 29393575)
-
(1999)
Cancer Research
, vol.59
, Issue.16
, pp. 4042-4049
-
-
Yamori, T.1
Matsunaga, A.2
Sato, S.3
Yamazaki, K.4
Komi, A.5
Ishizu, K.6
Mita, I.7
Edatsugi, H.8
Matsuba, Y.9
Takezawa, K.10
Nakanishi, O.11
Kohno, H.12
Nakajima, Y.13
Komatsu, H.14
Andoh, T.15
Tsuruo, T.16
-
33
-
-
33646447708
-
Antitumor activity of ZSTK474, a new phosphatidylinositol 3-kinase inhibitor
-
DOI 10.1093/jnci/djj133
-
Yaguchi, S.; Fukui, Y.; Koshimizu, I.; Yoshimi, H.; Matsuno T.; Gouda, H.; Hirono, S.; Yamazaki, K.; Yamori, T. Antitumor activity of ZSTK474, a new phosphatidylinositol 3-kinase inhibitor. J. Natl. Cancer Inst 2006, 98 (8), 545-556. (Pubitemid 43898818)
-
(2006)
Journal of the National Cancer Institute
, vol.98
, Issue.8
, pp. 545-556
-
-
Yaguchi, S.-I.1
Fukui, Y.2
Koshimizu, I.3
Yoshimi, H.4
Matsuno, T.5
Gouda, H.6
Hirono, S.7
Yamazaki, K.8
Yamori, T.9
-
34
-
-
33746904684
-
Expression and prognostic impact of the protein tyrosine phosphatases PRL-1, PRL-2, and PRL-3 in breast cancer
-
Radke, I.; Gotte, M.; Kersting, C.; Mattsson, B.; Kiesel, L.; Wulfing, P. Expression and prognostic impact of the protein tyrosine phosphatases PRL-1, PRL-2, and PRL-3 in breast cancer. Br. J. 2006, 95 (3), 347-354.
-
(2006)
Br. J.
, vol.95
, Issue.3
, pp. 347-354
-
-
Radke, I.1
Gotte, M.2
Kersting, C.3
Mattsson, B.4
Kiesel, L.5
Wulfing, P.6
-
35
-
-
0034651918
-
Breast cancer: Mechanisms and clinical application, a 1999 overview
-
Rochefort, H.; Garcia, M.; Glondu, M.; Laurent, V.; Liaudet, E.; Rey, J.-M.; Roger, P. Cathepsin. D in breast cancer: mechanisms and clinical application, a 1999 overview. Clin. Chim. Acta 2000, 291 (2), 157-170.
-
(2000)
Clin. Chim. Acta
, vol.291
, Issue.2
, pp. 157-170
-
-
Rochefort, H.1
Garcia, M.2
Glondu, M.3
Laurent, V.4
Liaudet, E.5
Rey, J.-M.6
Roger, P.7
Cathepsin, D.8
-
36
-
-
33646854205
-
Cathepsin D: Newly discovered functions of a long-standing aspartic protease in cancer and apoptosis
-
DOI 10.1016/j.canlet.2005.06.007, PII S0304383505005525
-
Liaudet-Coopman, E.; Beaujouin, M.; Derocq, D.; Garcia, M.; Glondu-Lassis, M.; Laurent-Matha, V.; Prébois, C.; Rochefort, H.; Vignon, F. Cathepsin D: newly discovered functions of a longstanding aspartic protease in cancer and apoptosis. Cancer Lett. 2006, 237(2), 167-179. (Pubitemid 43777078)
-
(2006)
Cancer Letters
, vol.237
, Issue.2
, pp. 167-179
-
-
Liaudet-Coopman, E.1
Beaujouin, M.2
Derocq, D.3
Garcia, M.4
Glondu-Lassis, M.5
Laurent-Matha, V.6
Prebois, C.7
Rochefort, H.8
Vignon, F.9
-
37
-
-
34548594517
-
Lysosomal cysteine proteinase cathepsin S as a potential target for anti-cancer therapy
-
Chang, W. S.; Wu, H. R.; Yeh, C. T.; Wu, C. W.; Chang, J. Y. Lysosomal cysteine proteinase cathepsin S as a potential target for anti-cancer therapy. J., Cancer Mol- 2007, 3, 5-14.
-
(2007)
J. Cancer Mol.
, vol.3
, pp. 5-14
-
-
Chang, W.S.1
Wu, H.R.2
Yeh, C.T.3
Wu, C.W.4
Chang, J.Y.5
-
38
-
-
35448969671
-
A receptor π subunit
-
A receptor π subunit. Cancer Res- 2007, 67, 9704-9712.
-
(2007)
Cancer Res.
, vol.67
, pp. 9704-9712
-
-
Takehara, A.1
Hosokawa, M.2
Eguchi, H.3
Ohigashi, H.4
Ishikawa, O.5
Nakamura, Y.6
Nakagawa, H.7
-
39
-
-
34848825642
-
CHM-1 inhibits hepatocyte growth factor-induced invasion of SKHep-1 human hepatocellular carcinoma cells by suppressing matrix metalloproteinase-9 expression
-
Wang, S. W.; Pan, S. L.; Peng, C. Y.; Huang, D. Y.; Tsai, A. C.; Chang, Y. L.; Guh, J. H.; Kuo, S. C.; Lee, K. H.; Teng, C. M. CHM-1 inhibits hepatocyte growth factor-induced invasion of SKHep-1 human hepatocellular carcinoma cells by suppressing matrix metalloproteinase-9 expression. Cancer Lett 2007, 257, 87-96.
-
(2007)
Cancer Lett
, vol.257
, pp. 87-96
-
-
Wang, S.W.1
Pan, S.L.2
Peng, C.Y.3
Huang, D.Y.4
Tsai, A.C.5
Chang, Y.L.6
Guh, J.H.7
Kuo, S.C.8
Lee, K.H.9
Teng, C.M.10
-
40
-
-
4344610852
-
Timing and checkpoints in the regulation, of mitotic progression
-
Meraldi, P.; Draviam, V. M.; Sorger, P. K. Timing and checkpoints in the regulation, of mitotic progression. Dev. Cell 2004, 7, 45-60.
-
(2004)
Dev. Cell
, vol.7
, pp. 45-60
-
-
Meraldi, P.1
Draviam, V.M.2
Sorger, P.K.3
-
41
-
-
0024312538
-
Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
-
Pauli, K. D.; Shoemaker, R. H.; Hodes L.; Monks, A.; Scudiero, D. A.; Rubinstein, L.; Plowman, J.; Boyd, M. R. Display and analysis of patterns of differential activity of drugs against human tumor cell lines: development of mean graph and COMPARE algorithm. J. Natl. Cancer Inst 1989, 81 (14), 1088-1092.
-
(1989)
J. Natl. Cancer Inst.
, vol.81
, Issue.14
, pp. 1088-1092
-
-
Pauli, K.D.1
Shoemaker, R.H.2
Hodes, L.3
Monks, A.4
Scudiero, D.A.5
Rubinstein, L.6
Plowman, J.7
Boyd, M.R.8
-
42
-
-
0025775062
-
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human, tumor cell lines
-
Monks, A.; Scudiero, D.; Skehan, P.; Shoemaker, R.; Pauli, K.; Vistica, D.; Hose, C.; Langley, J.; Cronise, P.; Vaigro-Wolff, A.; Gray-Goodrich, M.; Campbell, H.; Mayo, J.; Boyd, M. Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human, tumor cell lines. J. Natl. Cancer Inst. 1991, 83, 757-766.
-
(1991)
J. Natl. Cancer Inst.
, vol.83
, pp. 757-766
-
-
Monks, A.1
Scudiero, D.2
Skehan, P.3
Shoemaker, R.4
Pauli, K.5
Vistica, D.6
Hose, C.7
Langley, J.8
Cronise, P.9
Vaigro-Wolff, A.10
Gray-Goodrich, M.11
Campbell, H.12
Mayo, J.13
Boyd, M.14
-
43
-
-
0042827269
-
Panel of human cancer cell lines provides valuable database for drug discovery and bioinformatics
-
Yamori, T. Panel of human cancer cell lines provides valuable database for drug discovery and bioinformatics Cancer Che-mother, Pharmacol 2003, 2, S74-S79. (Pubitemid 37047027)
-
(2003)
Cancer Chemotherapy and Pharmacology, Supplement
, vol.52
, Issue.1
-
-
Yamori, T.1
-
44
-
-
0022649091
-
Tumor measurement in the nude mouse
-
Euhus, D. M.; Hudd, C.; LaRegina, M. C.; Johnson, F. E. Tumor measurement in the nude mouse. J. Surg. Oncol. 1986, 31, 229-234.
-
(1986)
J. Surg. Oncol.
, vol.31
, pp. 229-234
-
-
Euhus, D.M.1
Hudd, C.2
Laregina, M.C.3
Johnson, F.E.4
-
45
-
-
0024354304
-
Determination of subcutaneous tumor size in athymic (nude) mice
-
Tomayko, M. M.; Reynolds, C. P. Determination of subcutaneous tumor size in athymic (nude) mice. Cancer Chemother, Pharmacol. 1989, 24, 148-154.
-
(1989)
Cancer Chemother, Pharmacol.
, vol.24
, pp. 148-154
-
-
Tomayko, M.M.1
Reynolds, C.P.2
-
46
-
-
77649198179
-
-
References Provided in Supporting Information
-
References provided in Supporting Information.
-
-
-
|