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rdf:type |
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lifeskim:mentions |
umls-concept:C0001128,
umls-concept:C0166415,
umls-concept:C0184511,
umls-concept:C0231484,
umls-concept:C0242692,
umls-concept:C0243192,
umls-concept:C0392756,
umls-concept:C0879626,
umls-concept:C1552644,
umls-concept:C1554184,
umls-concept:C1823153,
umls-concept:C2349976
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pubmed:issue |
20
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pubmed:dateCreated |
2009-10-15
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pubmed:databankReference |
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pubmed:abstractText |
The preparation of a new series of 2-aryloxy-3-phenyl-propanoic acids, resulting from the introduction of a linker into the diphenyl system of the previously reported PPARalpha/gamma dual agonist 1, allowed the identification of new ligands with improved potency on PPARalpha and unchanged activity on PPARgamma. For the most interesting stereoisomers S-2 and S-4, X-ray studies in PPARgamma and docking experiments in PPARalpha provided a molecular explanation for their different behavior as full and partial agonists of PPARalpha and PPARgamma, respectively. Due to the adverse effects provoked by hypolipidemic drugs on skeletal muscle function, we also investigated the blocking activity of S-2 and S-4 on skeletal muscle membrane chloride channel conductance and found that these ligands have a pharmacological profile more beneficial compared to fibrates currently used in therapy.
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pubmed:language |
eng
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pubmed:journal |
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|
pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1520-4804
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pubmed:author |
pubmed-author:AntonioLaghezzaL,
pubmed-author:Conte CamerinoDianaD,
pubmed-author:FracchiollaGiuseppeG,
pubmed-author:LavecchiaAntonioA,
pubmed-author:LoiodiceFulvioF,
pubmed-author:MazzaFernandoF,
pubmed-author:MontanariRobertaR,
pubmed-author:NovellinoEttoreE,
pubmed-author:PiemonteseLucaL,
pubmed-author:PiernoSabataS,
pubmed-author:PochettiGiorgioG,
pubmed-author:TortorellaPaoloP
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pubmed:issnType |
Electronic
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pubmed:day |
22
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|
pubmed:volume |
52
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
6382-93
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pubmed:meshHeading |
pubmed-meshheading:19775169-Animals,
pubmed-meshheading:19775169-Cell Line, Tumor,
pubmed-meshheading:19775169-Chloride Channels,
pubmed-meshheading:19775169-Chlorides,
pubmed-meshheading:19775169-Clofibric Acid,
pubmed-meshheading:19775169-Crystallography, X-Ray,
pubmed-meshheading:19775169-Drug Discovery,
pubmed-meshheading:19775169-Electric Conductivity,
pubmed-meshheading:19775169-Humans,
pubmed-meshheading:19775169-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:19775169-Ligands,
pubmed-meshheading:19775169-Male,
pubmed-meshheading:19775169-Models, Molecular,
pubmed-meshheading:19775169-Molecular Conformation,
pubmed-meshheading:19775169-Muscle, Skeletal,
pubmed-meshheading:19775169-Muscular Diseases,
pubmed-meshheading:19775169-PPAR alpha,
pubmed-meshheading:19775169-PPAR gamma,
pubmed-meshheading:19775169-Propionic Acids,
pubmed-meshheading:19775169-Rats,
pubmed-meshheading:19775169-Rats, Wistar,
pubmed-meshheading:19775169-Rest,
pubmed-meshheading:19775169-Stereoisomerism,
pubmed-meshheading:19775169-Substrate Specificity
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pubmed:year |
2009
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pubmed:articleTitle |
New 2-aryloxy-3-phenyl-propanoic acids as peroxisome proliferator-activated receptors alpha/gamma dual agonists with improved potency and reduced adverse effects on skeletal muscle function.
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pubmed:affiliation |
Dipartimento Farmaco-Chimico, Università degli Studi di Bari, via Orabona 4, 70126 Bari, Italia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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