C. Yun

发表

Biosynthesis and Recycling of Nicotinamide Cofactors in Mycobacterium tuberculosis

D. Schnappinger, K. Pethe, L. Camacho, 2008, Journal of Biological Chemistry.

Zebrafish as a Screening Model for Testing the Permeability of Blood-Brain Barrier to Small Molecules.

Sunjoo Ahn, Dae-Seop Shin, C. Yun, 2017, Zebrafish.

Antimicrobial activity of novel 4H-4-oxoquinolizine compounds against extensively drug-resistant Acinetobacter baumannii strains.

Je Chul Lee, C. Yun, Hyejin Jeon, 2017, International journal of antimicrobial agents.

Design and Synthesis of Novel Pyrazolo[3,4‐d]pyrimidin‐1‐yl piperidine Derivatives as Bruton's Tyrosine Kinase Inhibitors

Jeong Hee Jeon, Chi-Hoon Park, H. Jung, 2017 .

Discovery of substituted pyrazol-4-yl pyridazinone derivatives as novel c-Met kinase inhibitors

Byung Jin Byun, Eun-Young Kim, Chi-Hoon Park, 2016, Archives of pharmacal research.

Novel 2,4-diaminopyrimidines bearing fused tricyclic ring moiety for anaplastic lymphoma kinase (ALK) inhibitor.

Chi-Hoon Park, C. Yun, H. Kim, 2017, Bioorganic & medicinal chemistry letters.

Novel 2,4-dianilino-5-fluoropyrimidine derivatives possessing ALK inhibitory activities

Chi-Hoon Park, H. Jung, C. Yun, 2014, Archives of pharmacal research.

Novel bis-ortho-alkoxy-para-piperazinesubstituted-2,4-dianilinopyrimidines (KRCA-0008) as potent and selective ALK inhibitors for anticancer treatment.

Chi-Hoon Park, H. Jung, C. Yun, 2013, Bioorganic & medicinal chemistry letters.

Discovery of substituted pyrazol-4-yl pyridazinone derivatives as novel c-Met kinase inhibitors

Chi-Hoon Park, H. Jung, C. Yun, 2016, Archives of Pharmacal Research.

Discovery of a Novel Chemical Scaffold Against Mutant Isocitrate Dehydrogenase 1 (IDH1)

H. Jeong, Sunjoo Ahn, Chi-Hoon Park, 2020, AntiCancer Research.

Discovery of substituted 6-pheny-3H-pyridazin-3-one derivatives as novel c-Met kinase inhibitors.

Eun-Young Kim, Chi-Hoon Park, H. Jung, 2014, Bioorganic & medicinal chemistry letters.

A natural compound, aristoyagonine, is identified as a potent bromodomain inhibitor by mid-throughput screening.

S. Pyo, Chi-Hoon Park, C. Chung, 2018, Biochemical and biophysical research communications.

Development of potent ALK inhibitor and its molecular inhibitory mechanism against NSCLC harboring EML4-ALK proteins.

H. Jeong, Chi-Hoon Park, H. Jung, 2015, Biochemical and biophysical research communications.

Different ways to transport ammonia in human and Mycobacterium tuberculosis NAD+ synthetases

B. Gerratana, T. Doukov, C. Yun, 2020, Nature Communications.

Discovery of a New Sulfonamide Hepatitis B Capsid Assembly Modulator.

C. Yun, Young-Sik Jung, A. Imran, 2020, ACS medicinal chemistry letters.

Minor modifications to ceritinib enhance anti-tumor activity in EML4-ALK positive cancer.

H. Jeong, Eun-Young Kim, Sunjoo Ahn, 2016, Cancer letters.

Replacing the terminal piperidine in ceritinib with aliphatic amines confers activities against crizotinib-resistant mutants including G1202R.

Sunjoo Ahn, Chi-Hoon Park, H. Jung, 2017, European journal of medicinal chemistry.

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

Sunjoo Ahn, Chi-Hoon Park, Minji Lee, 2016, Bioorganic & medicinal chemistry letters.

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

Sunjoo Ahn, Chi-Hoon Park, Minji Lee, 2015, Bioorganic & medicinal chemistry letters.

Design, Synthesis, and Evaluation of 2‐Anilino‐4‐(3,5‐dicarboxamidespiperidine)‐pyrimidines as Anaplastic Lymphoma Kinase Inhibitors

Chi-Hoon Park, C. Yun, C. Chae, 2015 .

Design and synthesis of novel 3-(benzo[d]oxazol-2-yl)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amine derivatives as selective G-protein-coupled receptor kinase-2 and -5 inhibitors.

H. Seo, H. Jung, C. Yun, 2013, Bioorganic & medicinal chemistry letters.

Novel 2,4-dianilino-5-fluoropyrimidine derivatives possessing ALK inhibitory activities

Chi-Hoon Park, H. Jung, C. Yun, 2013, Archives of Pharmacal Research.

Design, Synthesis, and Evaluation of 2,4‐Di(piperidine‐substituted‐anilino)pyrimidine Derivatives as ALK Inhibitors

Sunjoo Ahn, Chi-Hoon Park, H. Jung, 2015 .

Biosynthesis and Recycling of Nicotinamide Cofactors in Mycobacterium tuberculosis

D. Schnappinger, S. Ehrt, K. Tahlan, 2008, Journal of Biological Chemistry.