19 articles for YH Jung
The following articles (labelled with PubMed ID or TBD) are for your review
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Computer-aided identification of new histone deacetylase 6 selective inhibitor with anti-sepsis activity.

Sungkyunkwan University
Discovery and SAR of N-(1-((substituted piperidin-4-yl)methyl)-3-methoxypiperidin-4-yl)-2-methoxybenzamide derivatives: 5-Hydroxytryptamine receptor 4 agonist as a potent prokinetic agent.

Sungkyunkwan University
Discovery of novel 2-[2-(3-hydroxy-pyridin-2-yl)-thiazol-4-yl]-acetamide derivatives as HIF prolyl 4-hydroxylase inhibitors; SAR, synthesis and modeling evaluation.

Sungkyunkwan University
Discovery of (E)-5-(benzylideneamino)-1H-benzo[d]imidazol-2(3H)-one derivatives as inhibitors for PTK6.

Yonsei University
[(4-Hydroxyl-benzo[4,5]thieno[3,2-c]pyridine-3-carbonyl)-amino]-acetic acid derivatives; HIF prolyl 4-hydroxylase inhibitors as oral erythropoietin secretagogues.

Sungkyunkwan University
Synthesis and biological evaluation of pyrimidine-based dual inhibitors of human epidermal growth factor receptor 1 (HER-1) and HER-2 tyrosine kinases.

Hanmi Research Center
Design and synthesis of N(6)-substituted-4'-thioadenosine-5'-uronamides as potent and selective human A(3) adenosine receptor agonists.

Ewha Womans University
Alicyclic Ring Size Variation of 4-Phenyl-2-naphthoic Acid Derivatives as P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Synthesis and biological evaluation of novel N-benzyltriazolyl-hydroxamate derivatives as selective histone deacetylase 6 inhibitors.

Sungkyunkwan University
Synthesis and pharmacological characterization of multiply substituted 2H-chromene derivatives as P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Bridged Piperidine Analogues of a High Affinity Naphthalene-Based P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Synthesis and biological evaluation of novel purinyl quinazolinone derivatives as PI3Kδ-specific inhibitors for the treatment of hematologic malignancies.

Sungkyunkwan University
Structure activity relationship of 3-nitro-2-(trifluoromethyl)-2H-chromene derivatives as P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Structure-Activity Relationship of Heterocyclic P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
Biological Evaluation of 5'-(

National Institute of Diabetes and Digestive and Kidney Diseases
Synthesis and biological evaluation of quinoxaline derivatives as specific c-Met kinase inhibitors.

Sungkyunkwan University
Exploration of Alternative Scaffolds for P2Y

National Institute of Diabetes and Digestive and Kidney Diseases
P2Y

Saint Louis University School of Medicine
Structure-activity relationship study of thiazolyl-hydroxamate derivatives as selective histone deacetylase 6 inhibitors.

Sungkyunkwan University