K. Min

发表

Identification of arylsulfonamides as ExoU inhibitors.

Hyeyoung Min, Doran Kim, Jihae Baek, 2014, Bioorganic & medicinal chemistry letters.

The structure-activity relationships of mansonone F, a potent anti-MRSA sesquiterpenoid quinone: SAR studies on the C6 and C9 analogs.

Y. Suh, E. Choi, K. Min, 2006, Bioorganic & medicinal chemistry letters.

A derivative of imidazobenzimidazole, ML106, inhibits melanin synthesis via p38 MAPK activation.

S. Y. Kim, Kyoung-Chan Park, Dong-Seok Kim, 2014, Die Pharmazie.

Reactive oxygen species regulate the quiescence of CD34-positive cells derived from human embryonic stem cells.

K. Min, W. Suh, Sun-Hwa Song, 2014, Cardiovascular research.

Identification and characterization of small-molecule inducers of epidermal keratinocyte differentiation.

P. Schultz, N. Gray, J. Walker, 2007, ACS chemical biology.

Discovery of novel thienopyrimidine derivatives as LRRK2 inhibitors

K. Min, Jiwon Park, Soyeon Jang, 2021, Bulletin of the Korean Chemical Society.

Synthesis and biological activity of 2-cyanoacrylamide derivatives tethered to imidazopyridine as TAK1 inhibitors

Jiho Song, K. Min, K. Suh, 2020, Journal of enzyme inhibition and medicinal chemistry.

An Efficient Solid-Phase Synthesis of α-1,2,3-Triazoloamide Derivatives via Click Chemistry

K. Min, Y. Gong, Taeho Lee, 2011 .

Discovery of small molecules that enhance astrocyte differentiation in rat fetal neural stem cells.

Hyun-Jung Kim, Y. Suh, Jiho Song, 2011, Bioorganic & medicinal chemistry letters.

Discovery of novel pyrimidine and malonamide derivatives as TGR5 agonists.

Seung-Hyun Jung, Jisook Kim, Kiho Lee, 2014, Bioorganic & medicinal chemistry letters.

Exogenous Addition of 25‐Hydroxycholesterol Reduces Level of Very Long‐Chain Fatty Acids in X‐Linked Adrenoleukodystrophy

Jiho Jang, Dong-Wook Kim, Jiho Song, 2019, ChemistryOpen.

Synthesis and Biological Activity of Benzopyranyl Urea and Benzopyranyl Thiourea Derivatives as MDR Reversal Agents

K. Min, Y. Gong, Taeho Lee, 2012 .

Synthesis and biological evaluation of decursin, prantschimgin and their derivatives

K. Min, Yan Xia, Kyeong Lee, 2009 .

Efficient solid-phase synthesis of 2,4-disubstituted 5-carbamoyl-thiazole derivatives using a traceless support

Kwang-Hyeon Liu, J. Bae, K. Min, 2015 .

A versatile asymmetric synthesis of highly enantiomerically enriched 12(S)-HETE via a combination of enzymatic and chemical processes

Hyun-Ju Park, Seung‐Yong Seo, Yong-Sil Lee, 2002 .

Identification of aminosulfonylarylisoxazole as microRNA-31 regulators

Hyeyoung Min, Soowon Kang, Jiho Song, 2017, PloS one.

Synthesis of Vinyl Sulfone-tethered Proline Derivatives as Highly Selective Cathepsin S Inhibitors

Doran Kim, K. Min, Ji-Young Song, 2014 .

Synthesis of proline analogues as potent and selective cathepsin S inhibitors.

K. Min, Ji-Young Song, Y. H. Kim, 2013, Bioorganic & medicinal chemistry letters.

Asymmetric Total Synthesis of Fluvirucinine A1

Y. Suh, K. Min, Soon-Ai Kim, 1999 .

Structure‐Activity Relationship of 4,6‐Disubstituted Pyrimidines as EGFR and VEGFR‐2 Tyrosine Kinase Inhibitors

Jiho Song, K. Min, J. Lee, 2017 .

Pimarane cyclooxygenase 2 (COX-2) inhibitor and its structure-activity relationship.

Y. Suh, K. Min, J. Jung, 2001, Bioorganic & medicinal chemistry letters.

A novel class of highly potent multidrug resistance reversal agents: disubstituted adamantyl derivatives.

N. Kaur, Yinglan Jin, Kiho Lee, 2009, Bioorganic & medicinal chemistry letters.

Discovery of Highly Potent Multidrug Resistance (MDR) Reversal Agents: Aminosulfonylaryl Isoxazole Derivatives

E. K. Kim, Y. Suh, K. Min, 2009 .

Transetherification of 2,4-dimethoxynitrobenzene by aromatic nucleophilic substitution

K. Oh, Jiho Song, K. Min, 2017, PloS one.

Novel Effect of Thiourea/Urea Additives on the Nucleophilic Aromatic Substitution of 2,4‐Dimethoxynitrobenzene

Jiho Song, K. Min, Soyeon Jang, 2019, Bulletin of the Korean Chemical Society.

Total synthesis of (+)-Brefeldin A.

Hyun-Ju Park, Seung‐Yong Seo, Yong-Sil Lee, 2002, The Journal of organic chemistry.

Facile construction of the oxaphenalene skeleton by peri ring closure. Formal synthesis of mansonone F

Seung‐Yong Seo, Y. Suh, K. Min, 2000 .

Novel potent antagonists of transient receptor potential channel, vanilloid subfamily member 1: structure-activity relationship of 1,3-diarylalkyl thioureas possessing new vanilloid equivalents.

Jin Kwan Kim, S. Shin, Kwang-Ok Lee, 2005, Journal of medicinal chemistry.

Structure-Activity Relationship of Indole-Tethered Pyrimidine Derivatives that Concurrently Inhibit Epidermal Growth Factor Receptor and Other Angiokinases

Jakyung Yoo, Doran Kim, Jiho Song, 2015, PloS one.

Design, synthesis, and structure–activity relationship of carbamate-tethered aryl propanoic acids as novel PPARα/γ dual agonists

Hyun-Ju Park, Mi Kyung Kim, Jakyung Yoo, 2007 .

Synthesis and structural optimization of multiple H-bonding region of diarylalkyl (thio)amides as novel TRPV1 antagonists.

Jong-Wha Jung, Y. Suh, H. Kim, 2009, Bioorganic & medicinal chemistry.

Discovery of Novel TRPV1 Ligands through Rational Approach Based on Its Putative Endogenous Ligand, 12(S)-HPETE

Y. Suh, K. Min, Hwa-Soon Kim, 2010 .

Discovery of small molecules that inhibit melanogenesis via regulation of tyrosinase expression.

S. Y. Kim, Dong-Seok Kim, Jiho Song, 2012, Bioorganic & medicinal chemistry letters.

Versatile Synthesis of 2-Aryloxyalkyl-oxirane-2-carboxylate: Syntheses of Ethyl 2-[6-(3-Alkoxyphenoxy)hexyl]oxirane-2-carboxylates

S. Baek, Y. Suh, K. Min, 1998 .

Synthesis and Bioevaluation of 4,5,6,7-Tetrahydrobenzo[d]isoxazole Derivatives as Melanogenesis Inhibitors

Doran Kim, Jiho Song, K. Min, 2014 .

MMS 1001 inhibits melanin synthesis via ERK activation.

S. Y. Kim, Kyoung-Chan Park, Dong-Seok Kim, 2013, Die Pharmazie.

The Propionyl Ester of Lovastatin Decreases the Levels of Very Long Chain Fatty Acids in Fibroblasts Derived from Patients with X-linked Adrenoleukodystrophy

Dong-Wook Kim, Jiho Jang, Jiho Song, 2018, Bulletin of the Korean Chemical Society.

Computer-aided identification of ligands for GPCR anti-obesity targets.

Hyun-Ju Park, Jakyung Yoo, K. Min, 2009, Current topics in medicinal chemistry.

Click chemistry for improvement in selectivity of quinazoline-based kinase inhibitors for mutant epidermal growth factor receptors.

Jiho Song, K. Min, Soyeon Jang, 2019, Bioorganic & medicinal chemistry letters.

Synthesis of Quinazoline Analogues with Differential Activity for HER2‐overexpressing Breast Cancer Cells

K. Min, S. Jang, Y. H. Kim, 2015 .

Novel non-vanilloid VR1 antagonist of high analgesic effects and its structural requirement for VR1 antagonistic effects.

Jin Kwan Kim, Yong-Sil Lee, Y. Suh, 2003, Bioorganic & medicinal chemistry letters.

A synthetic small molecule that induces neuronal differentiation of adult hippocampal neural progenitor cells.

Peter G Schultz, Tomoko Kuwabara, Masaki Warashina, 2006, Angewandte Chemie.

A transcription factor hijacking to regulate RARα by using a chimeric molecule of retinoic acid and a DNA alkylator.

Hyun-Ju Park, Jiho Song, K. Min, 2011, Bioorganic & medicinal chemistry letters.

A small molecule accelerates neuronal differentiation in the adult rat

P. Schultz, H. Cline, B. Cravatt, 2010, Proceedings of the National Academy of Sciences.

Direct activation of capsaicin receptors by products of lipoxygenases: endogenous capsaicin-like substances.

S. Hwang, Y. Suh, H. Cho, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Isolation of a potent anti-MRSA sesquiterpenoid quinone from Ulmus davidiana var. japonica.

Y. Suh, E. Choi, H. S. Kim, 2000, Chemical & pharmaceutical bulletin.

Reactive oxygen species regulate the quiescence of CD 34-positive cells derived from human embryonic stem cells

K. Min, W. Suh, Kyungjong Kim, 2014 .

Synthesis and biological evaluation of novel thienopyrimidine derivatives as diacylglycerol acyltransferase 1 (DGAT-1) inhibitors

Seung-Hyun Jung, Jisook Kim, K. Min, 2019, Journal of enzyme inhibition and medicinal chemistry.

Design, synthesis, and biological evaluation of novel diarylalkyl amides as TRPV1 antagonists.

D. Kwon, Y. Suh, H. Kim, 2009, Bioorganic & medicinal chemistry.

Synthesis and anti-tumor activity of imidazopyrazines as TAK1 inhibitors.

K. Min, S. Jang, Y. H. Kim, 2019, European journal of medicinal chemistry.

Synthesis and anti-platelet activity of obovatol derivatives

Y. Yun, J. Hong, N. Choi, 2011, Archives of pharmacal research.

Methyl Aryloxy Gallates as Regulators of Vascular Smooth Muscle Cell Proliferation

S. Ahn, Y. Yun, J. Hong, 2009 .

The highly diastereoselective palladium-catalyzed cyclizations. stereoselective syntheses of cis and trans-disubstituted hydroxycyclopentanes

Y. Suh, K. Min, Soon-Ai Kim, 1997 .

Synthesis of lactam analog of 4-epi-brefeldin A

Seung‐Yong Seo, Y. Suh, Y. Chung, 2007 .

The Highly Diastereoselective Palladium-Catalyzed Cyclizations. Stereoselective Syntheses of cis- and trans-Disubstituted Hydroxycyclopentanes.

Y. Suh, K. Min, Soon-Ai Kim, 2010 .

Synthesis of Lactam Analogue of 4-epi-Brefeldin A.

Seung‐Yong Seo, Y. Suh, Y. Chung, 2007 .

Design, synthesis and cytotoxicity of chimeric erlotinib-alkylphospholipid hybrids.

Jongki Hong, Yong Sup Lee, Dong-Hyun Kim, 2019, Bioorganic chemistry.

Design, synthesis and evaluation of alkylphosphocholine-gefitinib conjugates as multitarget anticancer agents

Yong Sup Lee, Dong-Hyun Kim, K. Min, 2018, Archives of pharmacal research.

Identification of a Novel SHP-2 Protein Tyrosine Phosphatase Inhibitor

Sung Goo Park, Hyung-Kyoon Choi, B. Park, 2014 .

Structure-activity relationship of 7-aryl-2-anilino-pyrrolopyrimidines as Mer and Axl tyrosine kinase inhibitors

Jiho Song, K. Min, Jiwon Park, 2020, Journal of enzyme inhibition and medicinal chemistry.

Endogenous TRPV4 Expression of a Hybrid Neuronal Cell Line N18D3 and Its Utilization to Find a Novel Synthetic Ligand

S. Hwang, S. Yoo, Seung U. Kim, 2017, Journal of Molecular Neuroscience.

Discovery of orally active sulfonylphenyl thieno[3,2-d]pyrimidine derivatives as GPR119 agonists.

K. Min, Y. H. Kim, K. Suh, 2023, European journal of medicinal chemistry.

Synthesis of proline analogues as potent and selective cathepsin S inhibitors.

K. Min, Y. H. Kim, K. Suh, 2013, Bioorganic & medicinal chemistry letters.

Synthesis and Biological Evaluation of Biarylamide Derivatives as Inhibitors of Phagocytosis in Macrophages

Jiho Song, K. Min, K. Hwang, 2017 .

A novel class of highly potent multidrug resistance reversal agents: disubstituted adamantyl derivatives.

N. Kaur, Yinglan Jin, Kiho Lee, 2009, Bioorganic & medicinal chemistry letters.