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NSC 674495
Known as:
2-(4-amino-3-methylphenyl)benzothiazole
, NSC-674495
, DF 203
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
Aniline Compounds
Benzothiazoles
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Mechanisms of acquired resistance to 2-(4-Amino-3-methylphenyl)benzothiazole in breast cancer cell lines
T. Bradshaw
,
E. Stone
,
+4 authors
M. Stevens
Breast Cancer Research and Treatment
2008
Corpus ID: 26494677
Compounds within the 2-(4-aminophenyl)benzothiazole class represent extremely potent and selective experimental antitumour agents…
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Review
2004
Review
2004
The development of the antitumour benzothiazole prodrug, Phortress, as a clinical candidate.
T. Bradshaw
,
A. Westwell
Current Medicinal Chemistry
2004
Corpus ID: 40450610
This review traces the development of a series of potent and selective antitumour benzothiazoles from the discovery of the…
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Highly Cited
2003
Highly Cited
2003
Antitumour 2-(4-aminophenyl)benzothiazoles generate DNA adducts in sensitive tumour cells in vitro and in vivo
C. Leong
,
M. Gaskell
,
+7 authors
M. Stevens
British Journal of Cancer
2003
Corpus ID: 15051339
2-(4-Aminophenyl)benzothiazoles represent a potent and highly selective class of antitumour agent. In vitro, sensitive carcinoma…
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Highly Cited
2003
Highly Cited
2003
DNA damage and cell cycle arrest induced by 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole (5F 203, NSC 703786) is attenuated in aryl hydrocarbon receptor deficient MCF-7 cells
V. Trapani
,
V. Patel
,
+7 authors
A. Loaiza-Pérez
British Journal of Cancer
2003
Corpus ID: 9731895
The fluorinated benzothiazole analogue 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole (5F 203, NSC 703786) is a novel agent…
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2003
2003
Induction of CYP1A1 in tumor cells by the antitumor agent 2-[4-amino-3-methylphenyl]-5-fluoro-benzothiazole: a potential surrogate marker for patient sensitivity.
C. Hose
,
M. Hollingshead
,
E. Sausville
,
A. Monks
Molecular Cancer Therapeutics
2003
Corpus ID: 40520682
A candidate antitumor agent, 2-(4-amino-3-methylphenyl)-5-fluoro-benzothiazole (5F-203), like its non-fluorinated parent compound…
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Review
2001
Review
2001
The discovery of the potent and selective antitumour agent 2-(4-amino-3-methylphenyl)benzothiazole (DF 203) and related compounds.
T. Bradshaw
,
M. Stevens
,
A. Westwell
Current Medicinal Chemistry
2001
Corpus ID: 35463183
The development of a series of potent and selective antitumour agents, the 2-(4-aminophenyl)benzothiazoles, is described. The…
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Highly Cited
2000
Highly Cited
2000
Role of Cyp1A1 in modulation of antitumor properties of the novel agent 2-(4-amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) in human breast cancer cells.
Mei-Sze Chua
,
Eiji Kashiyama
,
+4 authors
M. Stevens
Cancer Research
2000
Corpus ID: 12063966
2-(4-Amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) is a candidate antitumor agent with potent and selective activity…
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2000
2000
Role of CYP 1 A 1 in Modulation of Antitumor Properties of the Novel Agent 2-( 4-Amino-3-methylphenyl ) benzothiazole ( DF 203 , NSC 674495 ) in Human Breast Cancer Cells 1
M. Chua
,
E. Kashiyama
,
+4 authors
M. Stevens
2000
Corpus ID: 43295827
2-(4-Amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) is a candidate antitumor agent with potent and selective activity…
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Highly Cited
1999
Highly Cited
1999
Antitumor benzothiazoles. 8. Synthesis, metabolic formation, and biological properties of the C- and N-oxidation products of antitumor 2-(4-aminophenyl)benzothiazoles.
Eiji Kashiyama
,
I. Hutchinson
,
+7 authors
Malcolm F. G. Stevens
Journal of Medicinal Chemistry
1999
Corpus ID: 10402588
2-(4-Aminophenyl)benzothiazoles 1 and their N-acetylated forms have been converted to C- and N-hydroxylated derivatives to…
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Highly Cited
1998
Highly Cited
1998
Influence of 2-(4-aminophenyl)benzothiazoles on growth of human ovarian carcinoma cells in vitro and in vivo.
TD Bradshaw
,
D. Shi
,
+7 authors
Mfg Stevens
British Journal of Cancer
1998
Corpus ID: 14836614
2-(4-Aminophenyl)benzothiazole molecules substituted in the 3 position of the phenyl ring with a halogen atom or methyl moiety…
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