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Chalcone and its analogs: Therapeutic and diagnostic applications in Alzheimer’s disease

Bioorganic chemistry, 2021-03, Vol.108, p.104681-104681, Article 104681

2021

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Retinoic acid signaling pathways in development and diseases

Bioorganic & medicinal chemistry, 2014-01, Vol.22 (2), p.673-683

2014

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NLRP3 Inflammasome Inhibitors for Antiepileptogenic Drug Discovery and Development

International journal of molecular sciences, 2024-06, Vol.25 (11), p.6078

2024

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Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines

Bioorganic & medicinal chemistry, 2010-05, Vol.18 (9), p.3066-3077

2010

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Dihydroxylated 2,4,6-triphenyl pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study

European journal of medicinal chemistry, 2012-03, Vol.49, p.219-228

2012

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Chalcone: A potential scaffold for NLRP3 inflammasome inhibitors

European journal of medicinal chemistry reports, 2023-04, Vol.7, p.100100, Article 100100

2023

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Design, synthesis, and antitumor evaluation of 2,4,6-triaryl pyridines containing chlorophenyl and phenolic moiety

European journal of medicinal chemistry, 2012-06, Vol.52, p.123-136

2012

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Folate-PEG Conjugates of a Far-Red Light-Activatable Paclitaxel Prodrug to Improve Selectivity toward Folate Receptor-Positive Cancer Cells

ACS omega, 2017-10, Vol.2 (10), p.6349-6360

2017

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2-Thienyl-4-furyl-6-aryl pyridine derivatives: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study

Bioorganic & medicinal chemistry, 2010, Vol.18 (1), p.377-386

2010

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2,4,6-Trisubstituted pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship

Bioorganic & medicinal chemistry, 2007-07, Vol.15 (13), p.4351-4359

2007

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Novel self-nanoemulsifying drug delivery system for enhanced solubility and dissolution of lutein

Archives of Pharmacal Research, 2010, 33(3), , pp.417-426

2010

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Synthesis and biological evaluation of 2-phenol-4-chlorophenyl-6-aryl pyridines as topoisomerase II inhibitors and cytotoxic agents

Bioorganic chemistry, 2016-06, Vol.66, p.145-159

2016

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Use of zebrafish in chemical biology and drug discovery

Future medicinal chemistry, 2013-11, Vol.5 (17), p.2103-2116

2013

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Novel self-nanoemulsifying drug delivery system for enhanced solubility and dissolution of lutein

Archives of pharmacal research, 2010-03, Vol.33 (3), p.417-426

2010

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2,4-Diaryl-5H-chromeno [4,3-b]pyridines: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

Bulletin of the Korean Chemical Society, 2012, 33(9), , pp.3103-3106

2012

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2,4-Diaryl Benzofuro[3,2-b]pyridine Derivatives: Design, Synthesis, and Evaluation of Topoisomerase Inhibitory Activity and Cytotoxicity

Bulletin of the Korean Chemical Society, 2013, 34(10), , pp.3073-3082

2013

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2,4-Diaryl-5,6-dihydro-1,10-phenanthrolines with Furyl or Thienyl Moiety at 4-Position: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

Bulletin of the Korean Chemical Society, 2012, 33(5), , pp.1769-1772

2012

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Far-Red Light-Activatable Prodrug of Paclitaxel for the Combined Effects of Photodynamic Therapy and Site-Specific Paclitaxel Chemotherapy

Journal of medicinal chemistry, 2016-04, Vol.59 (7), p.3204-3214

2016

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Synthesis, Topoisomerase I and II Inhibitory Activity, Cytotoxicity, and Structure-activity Relationship Study of Rigid Analogues of 2,4,6-Trisubstituted Pyridine Containing 5,6-Dihydrobenzo[h]quinoline Moiety

Bulletin of the Korean Chemical Society, 2011, 32(1), , pp.303-306

2011

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Singlet Oxygen Activatable Prodrugs of Paclitaxel, SN‐38, MMC and CA4: Nonmitochondria‐Targeted Prodrugs

Photochemistry and photobiology, 2022-03, Vol.98 (2), p.389-399

2022

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Synthesis, Topoisomerase I and II Inhibitory Activities, and Cytotoxicity of 4,6-Diaryl-2,4'-bipyridine Derivatives

Bulletin of the Korean Chemical Society, 2010, 31(6), , pp.1747-1750

2010

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Identification of a N7-guanine adduct of 1-bromopropane in calf thymus DNA by mass spectrometry

Molecular & Cellular Toxicology, 2016, 12(1), , pp.7-14

2016

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2,6-Dithienyl-4-arylpyridines: Synthesis, Topoisomerase I and II Inhibition and Structure-activity Relationship

Bulletin of the Korean Chemical Society, 2008, 29(8), , pp.1605-1608

2008

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Solid self-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidylcholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein

European journal of pharmaceutics and biopharmaceutics, 2011-10, Vol.79 (2), p.250-257

2011

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Efficient activation of a visible light-activatable CA4 prodrug through intermolecular photo-unclick chemistry in mitochondria

Chemical communications (Cambridge, England), 2017-02, Vol.53 (11), p.1884-1887

2017

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Chalcone and its analogs: Therapeutic and diagnostic applications in Alzheimer’s disease

Retinoic acid signaling pathways in development and diseases

NLRP3 Inflammasome Inhibitors for Antiepileptogenic Drug Discovery and Development

Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines

Dihydroxylated 2,4,6-triphenyl pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study

Chalcone: A potential scaffold for NLRP3 inflammasome inhibitors

Design, synthesis, and antitumor evaluation of 2,4,6-triaryl pyridines containing chlorophenyl and phenolic moiety

Folate-PEG Conjugates of a Far-Red Light-Activatable Paclitaxel Prodrug to Improve Selectivity toward Folate Receptor-Positive Cancer Cells

2-Thienyl-4-furyl-6-aryl pyridine derivatives: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study

2,4,6-Trisubstituted pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship

Novel self-nanoemulsifying drug delivery system for enhanced solubility and dissolution of lutein

Synthesis and biological evaluation of 2-phenol-4-chlorophenyl-6-aryl pyridines as topoisomerase II inhibitors and cytotoxic agents

Use of zebrafish in chemical biology and drug discovery

Novel self-nanoemulsifying drug delivery system for enhanced solubility and dissolution of lutein

2,4-Diaryl-5H-chromeno [4,3-b]pyridines: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

2,4-Diaryl Benzofuro[3,2-b]pyridine Derivatives: Design, Synthesis, and Evaluation of Topoisomerase Inhibitory Activity and Cytotoxicity

2,4-Diaryl-5,6-dihydro-1,10-phenanthrolines with Furyl or Thienyl Moiety at 4-Position: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

Far-Red Light-Activatable Prodrug of Paclitaxel for the Combined Effects of Photodynamic Therapy and Site-Specific Paclitaxel Chemotherapy

Synthesis, Topoisomerase I and II Inhibitory Activity, Cytotoxicity, and Structure-activity Relationship Study of Rigid Analogues of 2,4,6-Trisubstituted Pyridine Containing 5,6-Dihydrobenzo[h]quinoline Moiety

Singlet Oxygen Activatable Prodrugs of Paclitaxel, SN‐38, MMC and CA4: Nonmitochondria‐Targeted Prodrugs

Synthesis, Topoisomerase I and II Inhibitory Activities, and Cytotoxicity of 4,6-Diaryl-2,4'-bipyridine Derivatives

Identification of a N7-guanine adduct of 1-bromopropane in calf thymus DNA by mass spectrometry

2,6-Dithienyl-4-arylpyridines: Synthesis, Topoisomerase I and II Inhibition and Structure-activity Relationship

Solid self-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidylcholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein

Efficient activation of a visible light-activatable CA4 prodrug through intermolecular photo-unclick chemistry in mitochondria

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