Source:http://linkedlifedata.com/resource/pubmed/id/16087336
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
20
|
| pubmed:dateCreated |
2005-9-12
|
| pubmed:abstractText |
Diaryl-(4-piperidinyl)-pyrrole derivatives bearing hydroxylated N-alkyl substituents have been synthesized and evaluated as anticoccidial agents. High potency in Et-PKG inhibition and broad-spectrum anticoccidial activities have been observed on compounds, such as 4b and 5h, which are fully efficacious in vivo at 50 ppm in feed.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
|
| pubmed:issn |
0960-894X
|
| pubmed:author |
pubmed-author:BiftuTesfayeT,
pubmed-author:CrumleyTamiT,
pubmed-author:Darkin-RattraySandra JSJ,
pubmed-author:DulskiPaula MPM,
pubmed-author:FengDennisD,
pubmed-author:FisherMichaelM,
pubmed-author:GurnettAnneA,
pubmed-author:LeavittPenny SuePS,
pubmed-author:LiangGui-BaiGB,
pubmed-author:LiberatorPaul APA,
pubmed-author:MisuraAndrew SAS,
pubmed-author:QianXiaoxiaX,
pubmed-author:SamarasSamanthaS,
pubmed-author:SchmatzDennis MDM,
pubmed-author:WyvrattMatthewM,
pubmed-author:XXX
|
| pubmed:issnType |
Print
|
| pubmed:day |
15
|
| pubmed:volume |
15
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
4570-3
|
| pubmed:dateRevised |
2009-11-19
|
| pubmed:meshHeading | |
| pubmed:year |
2005
|
| pubmed:articleTitle |
Hydroxylated N-alkyl-4-piperidinyl-2,3-diarylpyrrole derivatives as potent broad-spectrum anticoccidial agents.
|
| pubmed:affiliation |
Merck Research Laboratories, Department of Medicinal Chemistry and Human and Animal Infectious Disease Research, Merck and Co., Inc., PO Box 2000, Rahway, NJ 07065, USA. gui-bai_liang@merck.com
|
| pubmed:publicationType |
Journal Article
|