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SN 23862
Known as:
SN-23862
National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2000
2000
Pharmacokinetics and metabolism of the nitrogen mustard bioreductive drug 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (SN 23862) and the corresponding aziridine (CB 1954) in KHT tumour…
P. Kestell
,
F. Pruijn
,
B. Siim
,
B. Palmer
,
W. Wilson
Cancer Chemotherapy and Pharmacology
2000
Corpus ID: 28015372
Purpose: To characterise the pharmacokinetics and metabolism in mice of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (SN…
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1996
1996
Synthesis and evaluation of 4-substituted analogues of 5-[N,N-bis (2-chloroethyl)amino]-2-nitrobenzamide as bioreductively activated prodrugs using an Escherichia coli nitroreductase.
G. Atwell
,
M. Boyd
,
+4 authors
W. Denny
Anti-Cancer Drug Design
1996
Corpus ID: 24080394
2,4-Dinitrobenzamide mustards, exemplified by the parent compound SN 23862 (2) are activated under aerobic conditions by an…
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Highly Cited
1994
Highly Cited
1994
Combining bioreductive drugs (SR 4233 or SN 23862) with the vasoactive agents flavone acetic acid or 5,6-dimethylxanthenone acetic acid.
Stephen Cliffe
,
Maryann L. Taylor
,
Michael D. Rutland
,
B. Baguley
,
Richard P. Hill
,
William R. Wilson
International Journal of Radiation Oncology…
1994
Corpus ID: 28809575
Highly Cited
1992
Highly Cited
1992
Hypoxia-selective antitumor agents. 5. Synthesis of water-soluble nitroaniline mustards with selective cytotoxicity for hypoxic mammalian cells.
B. Palmer
,
W. Wilson
,
S. Cliffe
,
W. Denny
Journal of Medicinal Chemistry
1992
Corpus ID: 1735542
Nitroaniline mustards have potential as hypoxia-selective cytotoxic agents, with reductive metabolism activating the nitrogen…
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