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Volumn 16, Issue 4, 2006, Pages 771-774

Concise and efficient asymmetric synthesis of (S)-2-ethylphenylpropanoic acid derivatives: Dual agonists for human peroxisome proliferator-activated receptor α and δ

Author keywords

Metabolic syndrome; PPAR ; PPAR ; Reductive amide alkylation

Indexed keywords

2 ETHYLPHENYLPROPANOIC ACID; OXAZOLIDINONE DERIVATIVE; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR AGONIST; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR DELTA; PHENYLPROPIONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 30344435617     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.11.029     Document Type: Article
Times cited : (21)

References (18)
  • 13
    • 30344434798 scopus 로고    scopus 로고
    • note
    • 79Br (M + H) 460.1132, found 460.1161. This compound was used without further purification.
  • 15
    • 30344438082 scopus 로고    scopus 로고
    • note
    • D -68.1 (c = 0.356, MeCN).
  • 16
    • 30344442264 scopus 로고    scopus 로고
    • note
    • D -58.3 (c = 0.114, MeCN).
  • 18
    • 30344452430 scopus 로고    scopus 로고
    • note
    • 2 in air. Transfections were performed by the calcium phosphate coprecipitation. Eight hours after transfection, ligands were added. Cells were harvested approximately 16-20 h after the treatment, and luciferase and β-galactosidase activities were assayed using a luminometer and a microplate reader. DNA cotransfection experiments included 50 ng reporter plasmid, 20 ng pCMX-β-galactosidase, 15 ng of each PPAR receptor, and pGEM carrier DNA for a total of 150 ng DNA per well in a 96-well plate. Luciferase data were normalized to an internal β-galactosidase control and represent means (±SD) of triplicate assays.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.