-
1
-
-
26044464329
-
Obstacles and opportunities in the clinical development of targeted therapeutics
-
Dy GK, Adjei AA. Obstacles and opportunities in the clinical development of targeted therapeutics. Prog Drug Res 2005;63:19-41 (Pubitemid 41406428)
-
(2005)
Progress in Drug Research
, vol.63
, pp. 19-41
-
-
Dy, G.K.1
Adjei, A.A.2
-
2
-
-
36549055697
-
Will targeted therapy hold its promise? An evidence-based review
-
DOI 10.1097/CCO.0b013e3282f44b12, PII 0000162220080100000016
-
Murdoch D, Sager J. Will targeted therapy hold its promise? An evidence-based review. Curr Opin Oncol 2008;20:104-111 (Pubitemid 350190989)
-
(2008)
Current Opinion in Oncology
, vol.20
, Issue.1
, pp. 104-111
-
-
Murdoch, D.1
Sager, J.2
-
3
-
-
34547122873
-
The convergent development of molecular-targeted drugs for cancer treatment and prevention
-
Lippman SM, Heymach JV. The convergent development of molecular-targeted drugs for cancer treatment and prevention. Clin Cancer Res 2007;13:4035-4041
-
(2007)
Clin Cancer Res
, vol.13
, pp. 4035-4041
-
-
Lippman, S.M.1
Heymach, J.V.2
-
4
-
-
34247857676
-
A remedy for biomarker addiction: Back to rational anticancer drug development
-
DOI 10.1038/ncponc0811, PII NCPONC0811
-
Youssoufian H, Rowinsky EK. A remedy for biomarker addiction: back to rational anticancer drug development. Nat Clin Pract Oncol 2007;4:264-265 (Pubitemid 46758780)
-
(2007)
Nature Clinical Practice Oncology
, vol.4
, Issue.5
, pp. 264-265
-
-
Youssoufian, H.1
Rowinsky, E.K.2
-
5
-
-
38949108587
-
Recent developments in taxane drug delivery
-
DOI 10.2174/156720108783331005
-
Safavy A. Recent developments in taxane drug delivery. Curr Drug Deliv 2008;5:42-54 (Pubitemid 351225633)
-
(2008)
Current Drug Delivery
, vol.5
, Issue.1
, pp. 42-54
-
-
Safavy, A.1
-
6
-
-
62549140767
-
Trends in the exploration of anticancer targets and strategies in enhancing the efficacy of drug targeting
-
Zhu F, Zheng CJ, Han LY, et al. Trends in the exploration of anticancer targets and strategies in enhancing the efficacy of drug targeting. Curr Mol Pharmacol 2008;1:213-232
-
(2008)
Curr Mol Pharmacol
, vol.1
, pp. 213-232
-
-
Zhu, F.1
Zheng, C.J.2
Han, L.Y.3
-
7
-
-
34147210060
-
Bioluminescent assays for high-throughput screening
-
DOI 10.1089/adt.2006.053
-
Fan F, Wood KV. Bioluminescent assays for high-throughput screening. Assay Drug Dev Technol 2007;5:127-136 (Pubitemid 46581246)
-
(2007)
Assay and Drug Development Technologies
, vol.5
, Issue.1
, pp. 127-136
-
-
Fan, F.1
Wood, K.V.2
-
8
-
-
0036511068
-
New paradigms in drug design and discovery
-
Review of modern aspects of drug design and discovery
-
Neamati N, Barchi JJ Jr. New paradigms in drug design and discovery. Curr Top Med Chem 2002;2:211-227 • Review of modern aspects of drug design and discovery
-
(2002)
Curr Top Med Chem
, vol.2
, pp. 211-227
-
-
Neamati, N.1
Barchi Jr., J.J.2
-
9
-
-
23144432272
-
Discovery and preclinical evaluation of a novel class of small-molecule compounds in hormone-dependent and -independent cancer cell lines
-
First study disclosing anticancer properties of a series of salicylhydrazides
-
Plasencia C, Dayam R, Wang Q, et al. Discovery and preclinical evaluation of a novel class of small-molecule compounds in hormone-dependent and -independent cancer cell lines. Mol Cancer Ther 2005;4:1105-1113 •• First study disclosing anticancer properties of a series of salicylhydrazides.
-
(2005)
Mol Cancer Ther
, vol.4
, pp. 1105-1113
-
-
Plasencia, C.1
Dayam, R.2
Wang, Q.3
-
10
-
-
35649023179
-
Discovery of novel non-cytotoxic salicylhydrazide containing HIV-1 integrase inhibitors
-
Al-Mawsawi LQ, Dayam R, Taheri L, et al. Discovery of novel non-cytotoxic salicylhydrazide containing HIV-1 integrase inhibitors. Bioorg Med Chem Lett 2007;17:6472-6475
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 6472-6475
-
-
Al-Mawsawi, L.Q.1
Dayam, R.2
Taheri, L.3
-
11
-
-
33751085637
-
Synthesis and antitumor activities of a series of novel quinoxalinhydrazides
-
First study describing an initial structure-activity relationship and cytotoxicity of a series of quinoxalinhydrazides
-
Grande F, Aiello F, Grazia OD, et al. Synthesis and antitumor activities of a series of novel quinoxalinhydrazides. Bioorg Med Chem 2007;15:288-294 • First study describing an initial structure-activity relationship and cytotoxicity of a series of quinoxalinhydrazides.
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 288-294
-
-
Grande, F.1
Aiello, F.2
Grazia, O.D.3
-
12
-
-
55949086031
-
Discovery of novel anticancer compounds based on a quinoxalinehydrazine pharmacophore
-
First part of a series of papers describing a detailed computational approach used in optimizing quinoxalinhydrazide leads by designing novel scaffolds
-
Deng J, Taheri L, Grande F, et al. Discovery of novel anticancer compounds based on a quinoxalinehydrazine pharmacophore. ChemMedChem 2008;3:1677-1686 • First part of a series of papers describing a detailed computational approach used in optimizing quinoxalinhydrazide leads by designing novel scaffolds.
-
(2008)
ChemMedChem
, vol.3
, pp. 1677-1686
-
-
Deng, J.1
Taheri, L.2
Grande, F.3
-
13
-
-
62549161329
-
Elucidation of the molecular mechanisms of a salicylhydrazide class of compounds by proteomic analysis
-
In press A proteomic approach to understand the mechanism of action of salicylhydrazides
-
Cao X, Plasencia C, Kanzaki A, et al. Elucidation of the molecular mechanisms of a salicylhydrazide class of compounds by proteomic analysis. Curr Cancer Drug Targets 2009. In press • A proteomic approach to understand the mechanism of action of salicylhydrazides.
-
(2009)
Curr Cancer Drug Targets
-
-
Cao, X.1
Plasencia, C.2
Kanzaki, A.3
-
14
-
-
67650281087
-
Combination effects of SC144 and cytotoxic anti-cancer agents
-
In press First details of synergistic studies between a lead quinoxalinhydrazide and conventional drugs
-
Oshima T, Cao X, Grande F, et al. Combination effects of SC144 and cytotoxic anti-cancer agents. Anti Cancer Drugs 2009. In press • First details of synergistic studies between a lead quinoxalinhydrazide and conventional drugs.
-
(2009)
Anti Cancer Drugs
-
-
Oshima, T.1
Cao, X.2
Grande, F.3
-
15
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
DOI 10.1016/S1056-8719(00)00107-6, PII S1056871900001076
-
Lipinski CA. Drug-like properties and the causes of poor solubility and poor permeability. J Pharmacol Toxicol Methods 2000;44:235-249 (Pubitemid 32239479)
-
(2000)
Journal of Pharmacological and Toxicological Methods
, vol.44
, Issue.1
, pp. 235-249
-
-
Lipinski, C.A.1
-
16
-
-
0021933379
-
Comparative properties of five human ovarian adenocarcinoma cell lines
-
Buick RN, Pullano R, Trent JM. Comparative properties of five human ovarian adenocarcinoma cell lines. Cancer Res 1985;45:3668-3676 (Pubitemid 15226443)
-
(1985)
Cancer Research
, vol.45
, Issue.8
, pp. 3668-3676
-
-
Buick, R.N.1
Pullano, R.2
Trent, J.M.3
-
17
-
-
0027423911
-
Cross-resistance to diverse drugs is associated with primary cisplatin resistance in ovarian cancer cell lines
-
Hamaguchi K, Godwin AK, Yakushiji M, et al. Cross-resistance to diverse drugs is associated with primary cisplatin resistance in ovarian cancer cell lines. Cancer Res 1993;53:5225-5232
-
(1993)
Cancer Res
, vol.53
, pp. 5225-5232
-
-
Hamaguchi, K.1
Godwin, A.K.2
Yakushiji, M.3
-
18
-
-
0023130372
-
Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of chemosensitivity testing
-
Carmichael J, DeGraff WG, Gazdar AF, et al. Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res 1987;47:936-942
-
(1987)
Cancer Res
, vol.47
, pp. 936-942
-
-
Carmichael, J.1
DeGraff, W.G.2
Gazdar, A.F.3
-
20
-
-
0024416540
-
Pyrido[3,4-e]-1,2,4-triazines and related heterocycles as potential antifungal agents
-
Reich MF, Fabio PF, Lee VJ, et al. Pyrido[3,4-e]-1,2,4-triazines and related heterocycles as potential antifungal agents. J Med Chem 1989;32:2474-2485
-
(1989)
J Med Chem
, vol.32
, pp. 2474-2485
-
-
Reich, M.F.1
Fabio, P.F.2
Lee, V.J.3
-
21
-
-
0032749316
-
Pyrroloquinoxaline derivatives as high-affinity and selective 5-HT(3) receptor agonists: Synthesis, further structure-activity relationships, and biological studies
-
Campiani G, Morelli E, Gemma S, et al. Pyrroloquinoxaline derivatives as high-affinity and selective 5-HT(3) receptor agonists: synthesis, further structure-activity relationships, and biological studies. J Med Chem 1999;42:4362-4379
-
(1999)
J Med Chem
, vol.42
, pp. 4362-4379
-
-
Campiani, G.1
Morelli, E.2
Gemma, S.3
-
22
-
-
11144354006
-
Synthesis, antimalarial activity, and molecular modeling of new pyrrolo[1,2-a]quinoxalines, bispyrrolo[1,2-a]quinoxalines, bispyrido[3,2-e] pyrrolo[1,2-a] pyrazines, and bispyrrolo[1,2-a]thieno[3,2-e]pyrazines
-
Guillon J, Grellier P, Labaied M, et al. Synthesis, antimalarial activity, and molecular modeling of new pyrrolo[1,2-a]quinoxalines, bispyrrolo[1,2-a]quinoxalines, bispyrido[3,2-e]pyrrolo[1,2-a] pyrazines, and bispyrrolo[1,2-a]thieno[3,2-e]pyrazines. J Med Chem 2004;47:1997-2009
-
(2004)
J Med Chem
, vol.47
, pp. 1997-2009
-
-
Guillon, J.1
Grellier, P.2
Labaied, M.3
-
23
-
-
3543021476
-
Efficient method for the synthesis of hetarenoindanones based on 3-arylhetarenes and their conversion into hetarenoindenes
-
DOI 10.1021/jo049504w
-
Kashulin IA, Nifant'ev IE. Efficient method for the synthesis of hetarenoindanones based on 3-arylhetarenes and their conversion into hetarenoindenes. J Org Chem 2004;69:5476-5479 (Pubitemid 39014386)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.16
, pp. 5476-5479
-
-
Kashulin, I.A.1
Nifant'Ev, I.E.2
-
24
-
-
0032442522
-
Histone H3 phosphorylation is required for the initiation, but not maintenance, of mammalian chromosome condensation
-
Van Hooser A, Goodrich DW, Allis CD, et al. Histone H3 phosphorylation is required for the initiation, but not maintenance, of mammalian chromosome condensation. J Cell Sci 1998;111( Pt 23):3497-3506 (Pubitemid 29015387)
-
(1998)
Journal of Cell Science
, vol.111
, Issue.23
, pp. 3497-3506
-
-
Van Hooser, A.1
Goodrich, D.W.2
David Allis, C.3
Brinkley, B.R.4
Mancini, M.A.5
-
25
-
-
66149149868
-
Discovery of a novel quinoxalinhydrazide with a broad-spectrum anticancer activity
-
First disclosure of in vivo efficacy and broad-spectrum anticancer activity of a lead quinoxalinhydrazide
-
Plasencia C, Grande F, Oshima T, et al. Discovery of a novel quinoxalinhydrazide with a broad-spectrum anticancer activity. Cancer Biol Ther 2009;8:458-465 • First disclosure of in vivo efficacy and broad-spectrum anticancer activity of a lead quinoxalinhydrazide.
-
(2009)
Cancer Biol Ther
, vol.8
, pp. 458-465
-
-
Plasencia, C.1
Grande, F.2
Oshima, T.3
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