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

Nature communications, 2020-01, Vol.11 (1), p.16-16, Article 16

2020

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Altered small-world property of a dynamic metabolic network in murine left hippocampus after exposure to acute stress

Scientific reports, 2022-03, Vol.12 (1), p.3885-3885, Article 3885

2022

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Effect of Denoising and Deblurring 18F-Fluorodeoxyglucose Positron Emission Tomography Images on a Deep Learning Model’s Classification Performance for Alzheimer’s Disease

Metabolites, 2022-03, Vol.12 (3), p.231

2022

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Dynamic Variation in Hippocampal Metabolism after Acute Stress Exposure: An In Vivo Proton Magnetic Resonance Spectroscopy Study at 9.4 T

Journal of spectroscopy (Hindawi), 2021, Vol.2021, p.1-11

2021

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Nanoparticle-Assisted Visualization of Binding Interactions between Collagen Mimetic Peptide and Collagen Fibers

Angewandte Chemie (International ed.), 2006-03, Vol.45 (14), p.2267-2270

2006

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Image restoration algorithm incorporating methods to remove noise and blurring from positron emission tomography imaging for Alzheimer's disease diagnosis

Physica medica, 2022-11, Vol.103, p.181-189

2022

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

Bulletin of the Korean Chemical Society, 2017, 38(2), , pp.278-281

2017

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

Bulletin of the Korean Chemical Society, 2015, 36(7), , pp.1929-1932

2015

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

Bulletin of the Korean Chemical Society, 2015, 36(9), , pp.2397-2400

2015

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

Anticancer research, 2020-09, Vol.40 (9), p.4929-4935

2020

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

Biochemical and biophysical research communications, 2018-09, Vol.503 (2), p.882-887

2018

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Biosynthesis and Recycling of Nicotinamide Cofactors in Mycobacterium tuberculosis: AN ESSENTIAL ROLE FOR NAD IN NONREPLICATING BACILLI

The Journal of biological chemistry, 2008-07, Vol.283 (28), p.19329-19341

2008

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

European journal of medicinal chemistry, 2017-01, Vol.126, p.536-549

2017

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

International journal of antimicrobial agents, 2017-01, Vol.49 (1), p.107-111

2017

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Discovery of novel tetrahydroisoquinoline-containing pyrimidines as ALK inhibitors

Bioorganic & medicinal chemistry, 2016-01, Vol.24 (2), p.207-219

2016

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

Cancer letters, 2016-05, Vol.374 (2), p.272-278

2016

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

Bioorganic & medicinal chemistry letters, 2013-11, Vol.23 (22), p.6192-6196

2013

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Corrigendum to “Discovery of substituted 6-pheny-3H-pyridazin-3-one derivatives as novel c-Met kinase inhibitors” [Bioorg. Med. Chem. Lett. 24 (2014) 5093–5097]

Bioorganic & medicinal chemistry letters, 2017-07, Vol.27 (14), p.3205-3205

2017

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B-Alkyl Suzuki−Miyaura Cross-Coupling Reactions with Air-Stable Potassium Alkyltrifluoroborates

Journal of organic chemistry, 2003-07, Vol.68 (14), p.5534-5539

2003

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

Bioorganic & medicinal chemistry letters, 2014-11, Vol.24 (21), p.5093-5097

2014

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

Biochemical and biophysical research communications, 2015-08, Vol.464 (3), p.762-767

2015

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

Archives of Pharmacal Research, 2016, 39(4), , pp.453-464

2016

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Zebrafish as a screening model for testing the permeability of blood-brain barrier to small molecules

Drug metabolism and pharmacokinetics, 2019-01, Vol.34 (1), p.S35-S35

2019

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

Archives of Pharmacal Research, 2014, 37(7), , pp.873-881

2014

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Cross-coupling reactions of primary alkylboronic acids with aryl triflates and aryl halides

Tetrahedron, 2002-02, Vol.58 (8), p.1465-1470

2002

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

Altered small-world property of a dynamic metabolic network in murine left hippocampus after exposure to acute stress

Effect of Denoising and Deblurring 18F-Fluorodeoxyglucose Positron Emission Tomography Images on a Deep Learning Model’s Classification Performance for Alzheimer’s Disease

Dynamic Variation in Hippocampal Metabolism after Acute Stress Exposure: An In Vivo Proton Magnetic Resonance Spectroscopy Study at 9.4 T

Nanoparticle-Assisted Visualization of Binding Interactions between Collagen Mimetic Peptide and Collagen Fibers

Image restoration algorithm incorporating methods to remove noise and blurring from positron emission tomography imaging for Alzheimer's disease diagnosis

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

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

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

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

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

Biosynthesis and Recycling of Nicotinamide Cofactors in Mycobacterium tuberculosis: AN ESSENTIAL ROLE FOR NAD IN NONREPLICATING BACILLI

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

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

Discovery of novel tetrahydroisoquinoline-containing pyrimidines as ALK inhibitors

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

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

Corrigendum to “Discovery of substituted 6-pheny-3H-pyridazin-3-one derivatives as novel c-Met kinase inhibitors” [Bioorg. Med. Chem. Lett. 24 (2014) 5093–5097]

B-Alkyl Suzuki−Miyaura Cross-Coupling Reactions with Air-Stable Potassium Alkyltrifluoroborates

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

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

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

Zebrafish as a screening model for testing the permeability of blood-brain barrier to small molecules

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

Cross-coupling reactions of primary alkylboronic acids with aryl triflates and aryl halides

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