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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1999-1-14
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pubmed:abstractText |
A number of novel propargylic sulfone conjugates 3 and 4 with intercalating moieties were synthesized and evaluated for DNA cleavage activity through nucleic base alkylation. A remarkable enhancement in DNA cleaving potency was observed with those conjugates 3 possessing a suitable spacer, a right attachment point at the aromatic ring, and a good intercalator.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
20
|
pubmed:volume |
8
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
169-74
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9871648-Alkynes,
pubmed-meshheading:9871648-Bacteriophage phi X 174,
pubmed-meshheading:9871648-DNA, Viral,
pubmed-meshheading:9871648-Electrophoresis, Agar Gel,
pubmed-meshheading:9871648-Hydrolysis,
pubmed-meshheading:9871648-Intercalating Agents,
pubmed-meshheading:9871648-Isatin
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pubmed:year |
1998
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pubmed:articleTitle |
Remarkable tethering effect on DNA cleavage of propargylic sulfone conjugates with intercalating moieties.
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pubmed:affiliation |
Department of Chemistry, Hong Kong University of Science and Technology, Kowloon, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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