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Design, Synthesis, and Biological Evaluation of Novel Constrained meta-Substituted Phenyl Propanoic Acids as Peroxisome Proliferator-Activated Receptor α and γ Dual Agonists

Journal of medicinal chemistry, 2008-10, Vol.51 (20), p.6318-6333

2008

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PAR-1622 is a selective peroxisome proliferator-activated receptor γ partial activator with preserved antidiabetic efficacy and broader safety profile for fluid retention

Archives of Pharmacal Research, 2009, 32(5), , pp.721-727

2009

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Quantification of a novel PPARγ partial agonist (S)-2-ethoxy-3-(4-{3-methyl-5-[4-(3-methyl-isoxazol-5-yl)-phenyl]thiophen-2-ylmethoxy}-phenyl)-propionic acid (PAM-1616) in rat plasma using liquid chromatography-tandem mass spectrometry

Archives of Pharmacal Research, 2010, 33(9), , pp.1389-1394

2010

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Liquid chromatography-tandem mass spectrometry of a new PPARα/γ dual agonist PAR-5359 in rat plasma

Archives of Pharmacal Research, 2009, 32(12), , pp.1743-1748

2009

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PAM-1616, a selective peroxisome proliferator-activated receptor γ modulator with preserved anti-diabetic efficacy and reduced adverse effects

European journal of pharmacology, 2011-01, Vol.650 (2), p.673-681

2011

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Design, synthesis, and structure–activity relationship of carbamate-tethered aryl propanoic acids as novel PPARα/γ dual agonists

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (13), p.3595-3598

2007

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Transcription factor Sp1 is involved in expressional regulation of coxsackie and adenovirus receptor in cancer cells

BioMed research international, 2011-01, Vol.2011 (1), p.636497

2011

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Anti-Diabetic Effects of DA-11004, a Synthetic IDPc Inhibitor in High Fat High Sucrose Diet-Fed C57BL/6J Mice

Archives of Pharmacal Research, 2004, 27(1), , pp.48-52

2004

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Anti-diabetic effects of DA-11004, a synthetic IDPc inhibitor in high fat high sucrose diet-fed C57BL/6J mice

Archives of pharmacal research, 2004-01, Vol.27 (1), p.48-52

2004

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PAR-5359, a well-balanced PPARα/γ dual agonist, exhibits equivalent antidiabetic and hypolipidemic activities in vitro and in vivo

European journal of pharmacology, 2008-10, Vol.595 (1), p.119-125

2008

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An Efficient Process of Ondansetron Synthesis

Heterocycles, 1997, Vol.45 (10), p.2041

1997

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Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARα/γ dual agonists

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (18), p.4993-4996

2008

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Liquid chromatography-tandem mass spectrometry of a new PPARalpha/gamma dual agonist PAR-5359 in rat plasma

Archives of pharmacal research, 2009-12, Vol.32 (12), p.1743-1748

2009

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PAR-5359, a well-balanced PPARalpha/gamma dual agonist, exhibits equivalent antidiabetic and hypolipidemic activities in vitro and in vivo

European journal of pharmacology, 2008-10, Vol.595 (1-3), p.119-125

2008

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Design, synthesis, and structure-activity relationship of carbamate-tethered aryl propanoic acids as novel PPARalpha/gamma dual agonists

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (13), p.3595-3598

2007

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Facile Conversion of Carboxamides to Nitriles

Bulletin of the Korean Chemical Society, 1993, Vol.14 (2), p.301-302

1993

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Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARalpha/gamma dual agonists

Bioorganic & medicinal chemistry letters, 2008-09, Vol.18 (18), p.4993-4996

2008

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A synthetic approach to (+)-brefeldin A

Tetrahedron letters, 1995-07, Vol.36 (28), p.5035-5036

1995

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PAR-5359, a well-balanced PPARa/γ dual agonist, exhibits equivalent antidiabetic and hypolipidemic activities in vitro and in vivo

European journal of pharmacology, 2008, Vol.595 (1-3), p.119-125

2008

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A stereoselective synthesis of (±)-elemol via an intramolecular SN2' ester enolate alkylation

Tetrahedron letters, 1993-10, Vol.34 (41), p.6557-6558

1993

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Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARa/y dual agonists

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (18), p.4993-4996

2008

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A stereoselective synthesis of (±)-elemol via an intramolecular S N2′ ester enolate alkylation

Tetrahedron letters, 1993, Vol.34 (41), p.6557-6558

1993

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Sestamibi 의 신규합성과 제제화에 따른 안정성 비교

Nuclear medicine and molecular imaging, 2001-10, Vol.35 (5), p.334

2001

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아졸을 포함하는 신규 세파로스포린 유도체의 합성 및 항균력

Yaghag-hoi-ji, 2000-08, Vol.44 (4), p.318-324

2000

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Interpretation discrepancies of abdominal imaging by on-call radiology residents: Evaluation of risk factors

PloS one, 2022-09, Vol.17 (9), p.e0274313-e0274313

2022

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Design, Synthesis, and Biological Evaluation of Novel Constrained meta-Substituted Phenyl Propanoic Acids as Peroxisome Proliferator-Activated Receptor α and γ Dual Agonists

PAR-1622 is a selective peroxisome proliferator-activated receptor γ partial activator with preserved antidiabetic efficacy and broader safety profile for fluid retention

Quantification of a novel PPARγ partial agonist (S)-2-ethoxy-3-(4-{3-methyl-5-[4-(3-methyl-isoxazol-5-yl)-phenyl]thiophen-2-ylmethoxy}-phenyl)-propionic acid (PAM-1616) in rat plasma using liquid chromatography-tandem mass spectrometry

Liquid chromatography-tandem mass spectrometry of a new PPARα/γ dual agonist PAR-5359 in rat plasma

PAM-1616, a selective peroxisome proliferator-activated receptor γ modulator with preserved anti-diabetic efficacy and reduced adverse effects

Design, synthesis, and structure–activity relationship of carbamate-tethered aryl propanoic acids as novel PPARα/γ dual agonists

Transcription factor Sp1 is involved in expressional regulation of coxsackie and adenovirus receptor in cancer cells

Anti-Diabetic Effects of DA-11004, a Synthetic IDPc Inhibitor in High Fat High Sucrose Diet-Fed C57BL/6J Mice

Anti-diabetic effects of DA-11004, a synthetic IDPc inhibitor in high fat high sucrose diet-fed C57BL/6J mice

PAR-5359, a well-balanced PPARα/γ dual agonist, exhibits equivalent antidiabetic and hypolipidemic activities in vitro and in vivo

An Efficient Process of Ondansetron Synthesis

Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARα/γ dual agonists

Liquid chromatography-tandem mass spectrometry of a new PPARalpha/gamma dual agonist PAR-5359 in rat plasma

PAR-5359, a well-balanced PPARalpha/gamma dual agonist, exhibits equivalent antidiabetic and hypolipidemic activities in vitro and in vivo

Design, synthesis, and structure-activity relationship of carbamate-tethered aryl propanoic acids as novel PPARalpha/gamma dual agonists

Facile Conversion of Carboxamides to Nitriles

Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARalpha/gamma dual agonists

A synthetic approach to (+)-brefeldin A

PAR-5359, a well-balanced PPARa/γ dual agonist, exhibits equivalent antidiabetic and hypolipidemic activities in vitro and in vivo

A stereoselective synthesis of (±)-elemol via an intramolecular SN2' ester enolate alkylation

Design, synthesis, and evaluation of novel aryl-tetrahydropyridine PPARa/y dual agonists

A stereoselective synthesis of (±)-elemol via an intramolecular S N2′ ester enolate alkylation

Sestamibi 의 신규합성과 제제화에 따른 안정성 비교

아졸을 포함하는 신규 세파로스포린 유도체의 합성 및 항균력

Interpretation discrepancies of abdominal imaging by on-call radiology residents: Evaluation of risk factors

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