Source:http://linkedlifedata.com/resource/pubmed/id/18066846
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10-12
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pubmed:dateCreated |
2007-12-10
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pubmed:abstractText |
Novel L-bicyclocarba-d4T (1), an enantiomer of D-N-MCd4T has been enantiopurely synthesized as a potent anti-HIV agent starting from (R)-epichlorohydrin using tandem alkylation, chemoselective reduction of ester in the presence of lactone functional group, Grignard reaction, RCM reaction, and Mitsunobu reaction as key steps. L-N-MCd4T (1) was found to be very potent anti-HIV-1 (EC(50) = 6.76 microg/mL) agent with no cytotoxicity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1525-7770
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1653-7
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pubmed:meshHeading | |
pubmed:year |
2007
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pubmed:articleTitle |
Asymmetric synthesis and biological activity of L-bicyclocarba-d4T.
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pubmed:affiliation |
College of Pharmacy and Research Institute for Drug Development, Pusan National University, San 30 Jangjeon-dong, Geumjeong-gu, Busan 609-735, Korea. mhr108@pusan.ac.kr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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