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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
|
pubmed:dateCreated |
1999-4-5
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pubmed:abstractText |
A series of gem-difluoro-avermectin derivatives was synthesized from the corresponding ketones at positions 4", 4', 13, and 23 using diethylaminosulfur trifluoride (DAST). These fluorinated avermectins exhibit potent antiparasitic activity in a new Haemonchus contortus larval assay and are equipotent to ivermectin. In addition, 23-gem-difluoro-ivermectin displays useful anticonvulsant activity in mouse models.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3643-6
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading | |
pubmed:year |
1998
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pubmed:articleTitle |
Synthesis of gem-difluoro-avermectin derivatives: potent anthelmintic and anticonvulsant agents.
|
pubmed:affiliation |
Merck Research Laboratories, Department of Medicinal Chemistry, Rahway, NJ 07065-0900, USA.
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pubmed:publicationType |
Journal Article
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