31 articles for S Ahn
The following articles (labelled with PubMed ID or TBD) are for your review
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Replacing the terminal piperidine in ceritinib with aliphatic amines confers activities against crizotinib-resistant mutants including G1202R.

Korea Research Institute of Chemical Technology
Novel 2,4-diaminopyrimidines bearing tetrahydronaphthalenyl moiety against anaplastic lymphoma kinase (ALK): Synthesis, in vitro, ex vivo, and in vivo efficacy studies.

Chungbuk National University
Synthesis and evaluation of novel 2,4-diaminopyrimidines bearing bicyclic aminobenzazepines for anaplastic lymphoma kinase (ALK) inhibitor.

Korea Research Institute of Chemical Technology
Serendipitous discovery of 2-((phenylsulfonyl)methyl)-thieno[3,2-d]pyrimidine derivatives as novel HIV-1 replication inhibitors.

Institut Pasteur Korea
Lead optimization of a novel series of imidazo[1,2-a]pyridine amides leading to a clinical candidate (Q203) as a multi- and extensively-drug-resistant anti-tuberculosis agent.

Institut Pasteur Korea
Polyphenols bearing cinnamaldehyde scaffold showing cell growth inhibitory effects on the cisplatin-resistant A2780/Cis ovarian cancer cells.

Konkuk University
Discovery ofβ2 Adrenergic Receptor Ligands Using Biosensor Fragment Screening of Tagged Wild-Type Receptor.

University of Dundee
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
Carbamate JNK3 Inhibitors Show Promise as Effective Treatments for Alzheimer's Disease: In Vivo Studies on Mouse Models.

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

Seoul National University
Novel linked butanolide dimer compounds increase adiponectin production during adipogenesis in human mesenchymal stem cells through peroxisome proliferator-activated receptor γ modulation.

Seoul National University
Alkaloids and Coumarins with Adiponectin-Secretion-Promoting Activities from the Leaves of

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

Seoul National University
Discovery of Benzopyridone-Based Transient Receptor Potential Vanilloid 1 Agonists and Antagonists and the Structural Elucidation of Their Activity Shift.

Seoul National University
Discovery of novel tetrahydroisoquinoline-containing pyrimidines as ALK inhibitors.

Korea Research Institute of Chemical Technology
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
Discovery of indane propanamides as potent and selective TRPV1 antagonists.

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
Colorectal anticancer activities of polymethoxylated 3-naphthyl-5-phenylpyrazoline-carbothioamides.

Konkuk University
Discovery of dual-acting opioid ligand and TRPV1 antagonists as novel therapeutic agents for pain.

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

Seoul National University
Chromenylchalcones with inhibitory effects on monoamine oxidase B.

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

Seoul National University
Polypharmacology of N

Sahmyook University
Ethynyl derivatives

Hoffmann-La Roche
Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases

Abbvie
Inhibition of angiogenesis-relevant receptor tyrosine kinases by sulindac analogues.

Max-Planck-Institut FÜR Molekulare Physiologie
Synthesis and biological evaluation of sulfonylhydrazone-substituted imidazo[1,2-a]pyridines as novel PI3 kinase p110alpha inhibitors.

Astellas Pharma