21 articles for S An
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Discovery of potent LPA2 (EDG4) antagonists as potential anticancer agents.

Amgen
Addressing PXR liabilities of phthalazine-based hedgehog/smoothened antagonists using novel pyridopyridazines.

Amgen
Design of 1-piperazinyl-4-arylphthalazines as potent Smoothened antagonists.

Amgen
Discovery of Ligands for TRIM58, a Novel Tissue-Selective E3 Ligase.

Novartis Institutes for Biomedical Research
Discovery of PPARγ and glucocorticoid receptor dual agonists to promote the adiponectin and leptin biosynthesis in human bone marrow mesenchymal stem cells.

Seoul National University
Structure-Activity Relationships of Truncated 1'-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs.

Seoul National University
Prenylated Chrysin Derivatives as Partial PPARγ Agonists with Adiponectin Secretion-Inducing Activity.

Seoul National University
Human ACAT inhibitory effects of shikonin derivatives from Lithospermum erythrorhizon.

National Research Laboratory of Lipid Metabolism and Atherosclerosis
Discovery of Pan-peroxisome Proliferator-Activated Receptor Modulators from an Endolichenic Fungus,

Seoul National University
Design, Synthesis, and Biological Activity of l-1'-Homologated Adenosine Derivatives.

Chonnam National University
Galangin 3-benzyl-5-methylether derivatives function as an adiponectin synthesis-promoting peroxisome proliferator-activated receptor γ partial agonist.

Seoul National University
Human ACAT-1 and -2 inhibitory activities of saucerneol B, manassantin A and B isolated from Saururus chinensis.

Korea Research Institute of Bioscience and Biotechnology
Discovery and Structure-Activity Relationships of Novel Template, Truncated 1'-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators.

Seoul National University
Kojyl cinnamate esters are peroxisome proliferator-activated receptor α/γ dual agonists.

Seoul National University
2-Phenyl-8-(1-phenylallyl)-chromenone compounds have a pan-PPAR modulator pharmacophore.

Seoul National University
Selenium bioisosteric replacement of adenosine derivatives promoting adiponectin secretion increases the binding affinity to peroxisome proliferator-activated receptor δ.

Seoul National University
Adiponectin-Secretion-Promoting Phenylethylchromones from the Agarwood of Aquilaria malaccensis.

Seoul National University
2-Formyl-komarovicine promotes adiponectin production in human mesenchymal stem cells through PPARγ partial agonism.

Seoul National University
Substituted heteroaryl compounds and methods of use

Calitor Sciences
Methyl/fluoro-pyridinyl-methoxy substituted pyridinone-pyridinyl compounds and fluoro-pyrimidinyl-methoxy substituted pyridinone-pyridinyl compounds

Confluence Life Sciences
Compounds that are ERK inhibitors

Merck Sharp & Dohme