These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
113 related articles for article (PubMed ID: 20219371)
1. Discovery of a novel selective PPARgamma modulator from (-)-Cercosporamide derivatives. Furukawa A; Arita T; Satoh S; Wakabayashi K; Hayashi S; Matsui Y; Araki K; Kuroha M; Ohsumi J Bioorg Med Chem Lett; 2010 Apr; 20(7):2095-8. PubMed ID: 20219371 [TBL] [Abstract][Full Text] [Related]
2. Substituents at the naphthalene C3 position of (-)-Cercosporamide derivatives significantly affect the maximal efficacy as PPARγ partial agonists. Furukawa A; Arita T; Fukuzaki T; Satoh S; Mori M; Honda T; Matsui Y; Wakabayashi K; Hayashi S; Araki K; Ohsumi J Bioorg Med Chem Lett; 2012 Feb; 22(3):1348-51. PubMed ID: 22225641 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and biological evaluation of novel (-)-Cercosporamide derivatives as potent selective PPARγ modulators. Furukawa A; Arita T; Fukuzaki T; Mori M; Honda T; Satoh S; Matsui Y; Wakabayashi K; Hayashi S; Nakamura K; Araki K; Kuroha M; Tanaka J; Wakimoto S; Suzuki O; Ohsumi J Eur J Med Chem; 2012 Aug; 54():522-33. PubMed ID: 22727448 [TBL] [Abstract][Full Text] [Related]
4. PAR-1622 is a selective peroxisome proliferator-activated receptor gamma partial activator with preserved antidiabetic efficacy and broader safety profile for fluid retention. Kim MK; Chae YN; Kim HS; Choi SH; Son MH; Kim SH; Kim JK; Moon HS; Park SK; Shin YA; Kim JG; Lee CH; Lim JI; Shin CY Arch Pharm Res; 2009 May; 32(5):721-7. PubMed ID: 19471887 [TBL] [Abstract][Full Text] [Related]
5. Discovery of novel dual functional agent as PPARgamma agonist and 11beta-HSD1 inhibitor for the treatment of diabetes. Ye YL; Zhou Z; Zou HJ; Shen Y; Xu TF; Tang J; Yin HZ; Chen ML; Leng Y; Shen JH Bioorg Med Chem; 2009 Aug; 17(15):5722-32. PubMed ID: 19574056 [TBL] [Abstract][Full Text] [Related]
6. Pyridine-2-propanoic acids: Discovery of dual PPARalpha/gamma agonists as antidiabetic agents. Humphries PS; Almaden JV; Barnum SJ; Carlson TJ; Do QQ; Fraser JD; Hess M; Kim YH; Ogilvie KM; Sun S Bioorg Med Chem Lett; 2006 Dec; 16(23):6116-9. PubMed ID: 16979341 [TBL] [Abstract][Full Text] [Related]
7. Sulfonylthiadiazoles with an unusual binding mode as partial dual peroxisome proliferator-activated receptor (PPAR) γ/δ agonists with high potency and in vivo efficacy. Keil S; Matter H; Schönafinger K; Glien M; Mathieu M; Marquette JP; Michot N; Haag-Diergarten S; Urmann M; Wendler W ChemMedChem; 2011 Apr; 6(4):633-53. PubMed ID: 21400663 [TBL] [Abstract][Full Text] [Related]
18. Development of a new class of benzoylpyrrole-based PPARα/γ activators. Ushiroda K; Maruta K; Kitoh M; Iwai K; Nagamine J; Tsuchida A; Taiji M; Nagata R Bioorg Med Chem Lett; 2011 Jan; 21(1):220-4. PubMed ID: 21130649 [TBL] [Abstract][Full Text] [Related]
19. Design and structural analysis of novel pharmacophores for potent and selective peroxisome proliferator-activated receptor gamma agonists. Lin CH; Peng YH; Coumar MS; Chittimalla SK; Liao CC; Lyn PC; Huang CC; Lien TW; Lin WH; Hsu JT; Cheng JH; Chen X; Wu JS; Chao YS; Lee HJ; Juo CG; Wu SY; Hsieh HP J Med Chem; 2009 Apr; 52(8):2618-22. PubMed ID: 19301897 [TBL] [Abstract][Full Text] [Related]