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19560918
Source:
http://linkedlifedata.com/resource/pubmed/id/19560918
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51
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0020792
,
umls-concept:C0023175
,
umls-concept:C0023688
,
umls-concept:C0031268
,
umls-concept:C0032743
,
umls-concept:C0082341
,
umls-concept:C0243076
pubmed:issue
16
pubmed:dateCreated
2009-7-29
pubmed:abstractText
The synthesis and SAR of a new series of potent and selective dopamine D(3) receptor antagonists is reported.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9107377
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Ether-A-Go-Go Potassium Channels
,
http://linkedlifedata.com/resource/pubmed/chemical/Imidazolidines
,
http://linkedlifedata.com/resource/pubmed/chemical/KCNH1 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands
,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D3
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1464-3405
pubmed:author
pubmed-author:FabioRomano DiRD
,
pubmed-author:GainesSimonS
,
pubmed-author:GentileGabriellaG
,
pubmed-author:HeidbrederChristianC
,
pubmed-author:HolmesIan PIP
,
pubmed-author:LorthioirOlivierO
,
pubmed-author:MicheliFabrizioF
,
pubmed-author:SavoiaChiaraC
,
pubmed-author:WatsonSteve PSP
,
pubmed-author:WorbyAngelaA
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4799-801
pubmed:meshHeading
pubmed-meshheading:19560918-Animals
,
pubmed-meshheading:19560918-Cats
,
pubmed-meshheading:19560918-Ether-A-Go-Go Potassium Channels
,
pubmed-meshheading:19560918-Humans
,
pubmed-meshheading:19560918-Imidazolidines
,
pubmed-meshheading:19560918-Ligands
,
pubmed-meshheading:19560918-Positron-Emission Tomography
,
pubmed-meshheading:19560918-Receptors, Dopamine D3
,
pubmed-meshheading:19560918-Structure-Activity Relationship
pubmed:year
2009
pubmed:articleTitle
Dopamine D3 receptor antagonists: the quest for a potentially selective PET ligand. Part one: lead identification.
pubmed:affiliation
Cancer Therapeutics, Melbourne, Australia.
pubmed:publicationType
Journal Article