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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1984-6-18
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pubmed:abstractText |
2-Haloethyl and ethyl (methylsulfonyl)methanesulfonates were prepared via sulfene intermediates. 2-Chloroethyl (methylsulfonyl)methanesulfonate is highly active against P388 leukemia in vivo; the majority of leukemic mice treated with this compound at 50 mg/kg per day, qd 1-5, survived more than 30 days and about 37% survived for more than 60 days. 2- Fluoroethyl (methylsulfonyl)methanesulfonate is also highly effective against P388 cells in vivo, but it is more toxic. Other (methylsulfonyl)methanesulfonate esters are more active than the analogous methanesulfonates and chloromethanesulfonates .
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
664-70
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6325693-Animals,
pubmed-meshheading:6325693-Antineoplastic Agents,
pubmed-meshheading:6325693-Drug Evaluation, Preclinical,
pubmed-meshheading:6325693-Indicators and Reagents,
pubmed-meshheading:6325693-Leukemia P388,
pubmed-meshheading:6325693-Magnetic Resonance Spectroscopy,
pubmed-meshheading:6325693-Mass Spectrometry,
pubmed-meshheading:6325693-Mesylates,
pubmed-meshheading:6325693-Mice,
pubmed-meshheading:6325693-Spectrophotometry, Infrared,
pubmed-meshheading:6325693-Structure-Activity Relationship
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pubmed:year |
1984
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pubmed:articleTitle |
2-Chloroethyl (methylsulfonyl)methanesulfonate and related (methylsulfonyl)methanesulfonates. Antineoplastic activity in vivo.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|