Source:http://linkedlifedata.com/resource/pubmed/id/20610151
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
14
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pubmed:dateCreated |
2010-7-8
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pubmed:abstractText |
A novel family of 1H-imidazol-2-yl-pyrimidine-4,6-diamines has been identified with potent activity against the erythrocyte-stage of Plasmodium falciparum (Pf), the most common causative agent of malaria. A systematic SAR study resulted in the identification of compound 40 which exhibits good potency against both wild-type and drug resistant parasites and exhibits good in vivo pharmacokinetic properties.
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pubmed:grant | |
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:month |
Jul
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pubmed:issn |
1464-3405
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pubmed:author |
pubmed-author:AdrianFranciscoF,
pubmed-author:ChangJonathanJ,
pubmed-author:ChatterjeeArnab KAK,
pubmed-author:ChenZhongZ,
pubmed-author:DengXianmingX,
pubmed-author:EkJaredJ,
pubmed-author:GrayNathanael SNS,
pubmed-author:HensonKerstinK,
pubmed-author:HowardStevenS,
pubmed-author:IsbellJohnJ,
pubmed-author:KuhenKelliK,
pubmed-author:NagleAdvaitA,
pubmed-author:PlouffeDavidD,
pubmed-author:SakataTomoyoT,
pubmed-author:SimersonSusanS,
pubmed-author:TullyDavid CDC,
pubmed-author:TuntlandToveT,
pubmed-author:WinzelerElizabethE,
pubmed-author:WuTaoT
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pubmed:copyrightInfo |
2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4027-31
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
Discovery of novel 1H-imidazol-2-yl-pyrimidine-4,6-diamines as potential antimalarials.
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pubmed:affiliation |
Department of Biological Chemistry & Molecular Pharmacology, Harvard Medical School, 250 Longwood Ave., SGM 628, Boston, MA 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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