Y. Jeong

发表

Tandem Dehydrogenation/Oxidation/Oxidative Cyclization Approach to Wrightiadione and Its Derivatives.

Y. Jeong, Y. Moon, Sungwoo Hong, 2015, Organic letters.

IPD-196, a novel phosphatidylinositol 3-kinase inhibitor with potent anticancer activity against hepatocellular carcinoma.

Ju-Hee Lee, Hyunseung Lee, Soon-Sun Hong, 2013, Cancer letters.

Suppression of tumor proliferation and angiogenesis of hepatocellular carcinoma by HS-104, a novel phosphoinositide 3-kinase inhibitor.

Soyoung Lee, Hyunseung Lee, Soon-Sun Hong, 2013, Cancer letters.

Changes in Gut Microbial Community of Pig Feces in Response to Different Dietary Animal Protein Media

Y. Jeong, Jongbin Park, E. Kim, 2020, Journal of microbiology and biotechnology.

Ru(II)-Catalyzed Site-Selective Hydroxylation of Flavone and Chromone Derivatives: The Importance of the 5-Hydroxyl Motif for the Inhibition of Aurora Kinases.

Jun Hee Lee, Y. Jeong, Sungwoo Hong, 2015, Organic letters.

Design and synthesis of imidazopyridine analogues as inhibitors of phosphoinositide 3-kinase signaling and angiogenesis.

Sungwoo Hong, Hyunseung Lee, Hyunseung Lee, 2011, Journal of medicinal chemistry.

Tandem Dehydrogenation/Oxidation/Oxidative Cyclization Approach to Wrightiadione and Its Derivatives.

Y. Jeong, Y. Moon, Sungwoo Hong, 2015, Organic letters.

Rh(III)-catalyzed direct C-H/C-H cross-coupling of quinones with arenes assisted by a directing group: identification of carbazole quinones as GSKβ inhibitors.

Y. Jeong, Y. Moon, Sungwoo Hong, 2015, Organic & biomolecular chemistry.

Identification of β-Lapachone Analogs as Novel MALT1 Inhibitors To Treat an Aggressive Subtype of Diffuse Large B-Cell Lymphoma.

Sungwoo Hong, Y. Jeong, H. Tae, 2015, Journal of medicinal chemistry.

A novel imidazopyridine derivative, HS-106, induces apoptosis of breast cancer cells and represses angiogenesis by targeting the PI3K/mTOR pathway.

Hyunseung Lee, Soon-Sun Hong, Sungwoo Hong, 2013, Cancer letters.

HS-173, a novel phosphatidylinositol 3-kinase (PI3K) inhibitor, has anti-tumor activity through promoting apoptosis and inhibiting angiogenesis.

Hyunseung Lee, Soon-Sun Hong, Sungwoo Hong, 2013, Cancer letters.

Structure-based de novo design and biochemical evaluation of novel BRAF kinase inhibitors.

Sungwoo Hong, Hwangseo Park, Hwangseo Park, 2012, Bioorganic & medicinal chemistry letters.

Strategies to overcome acquired resistances conferred by mutations in the kinase domain of EGFR.

Sungwoo Hong, Y. Jeong, S. M. Lim, 2016, Future medicinal chemistry.

Selective and potent small-molecule inhibitors of PI3Ks.

Sungwoo Hong, Y. Jeong, D. Kwon, 2014, Future medicinal chemistry.

Selectivity Enhancement Arising from Interactions at the PI3K Unique Pocket

Sun Choi, Yoonji Lee, Sungwoo Hong, 2012, ChemMedChem.

Omega-3-Rich Fish-Oil-Influenced Mouse Gut Microbiome Shaped by Intermittent Consumption of Beef

Y. Jeong, G. Han, Jongbin Park, 2023, Current Microbiology.

Discovery of wrightiadione as a novel template for the TrkA kinase inhibitors.

Sungwoo Hong, Y. Jeong, S. M. Lim, 2015, Bioorganic & medicinal chemistry letters.

Ligand-free monophasic CuPd alloys endows boosted reaction kinetics toward energy-efficient hydrogen fuel production paired with hydrazine oxidation

P. Show, H. Choi, J. Theerthagiri, 2022, Journal of Materials Science & Technology.

Aminoglycoside antibiotics bind to the influenza A virus RNA promoter.

G. Varani, Chin-Ju Park, Byong-Seok Choi, 2012, Molecular bioSystems.

A novel imidazopyridine analogue as a phosphatidylinositol 3-kinase inhibitor against human breast cancer.

Ju-Hee Lee, Hyunseung Lee, Soon-Sun Hong, 2012, Cancer letters.

Oxytocin modulation in the medial prefrontal cortex of pair-exposed rats during fear conditioning

Jihyun Noh, Y. Jeong, Minji Jang, 2022, Psychoneuroendocrinology.

Manifolding surface sites of compositional CoPd alloys via pulsed laser for hydrazine oxidation-assisted energy-saving electrolyzer: Activity origin and mechanism discovery

J. Theerthagiri, M. Y. Choi, Y. Jeong, 2023, Chemical Engineering Journal.

A novel imidazopyridine analogue as a phosphatidylinositol 3-kinase inhibitor against human breast cancer.

Ju-Hee Lee, Hyunseung Lee, Soon-Sun Hong, 2012, Cancer letters.

Rh(III)-catalyzed direct C-H/C-H cross-coupling of quinones with arenes assisted by a directing group: identification of carbazole quinones as GSKβ inhibitors.

Y. Jeong, Y. Moon, Sungwoo Hong, 2015, Organic & biomolecular chemistry.