Kyeojin Kim

发表

2-Aminophenylpyrimidines as Novel Inhibitors of Aminoacyl-tRNA Synthetase Interacting Multifunctional Protein 2 (AIMP2)-DX2 for Lung Cancer Treatment.

Dae Kim, Sunghoon Kim, Y. Suh, 2020, Journal of medicinal chemistry.

Topically Applied Taurine Chloramine Protects against UVB-Induced Oxidative Stress and Inflammation in Mouse Skin

Y. Surh, Y. Suh, Kyeojin Kim, 2021, Antioxidants.

Diastereoselective Total Synthesis of (-)-Galiellalactone.

Jeeyeon Lee, Y. Suh, Kyeojin Kim, 2015, The Journal of organic chemistry.

Identification and Structural Analysis of New Nrf2 Activators by Mechanism‐Based Chemical Transformation of 15‐Deoxy‐Δ12, 14‐PGJ2

Jeeyeon Lee, Y. Surh, Hyun-Ju Park, 2016, Chembiochem : a European journal of chemical biology.

Role of heme oxygenase-1 in potentiation of phagocytic activity of macrophages by taurine chloramine: Implications for the resolution of zymosan A-induced murine peritonitis.

Y. Surh, Y. Suh, Kyeojin Kim, 2018, Cellular immunology.

Sac-0601 prevents retinal vascular leakage in a mouse model of diabetic retinopathy.

Y. Suh, Kyeojin Kim, Young-Guen Kwon, 2011, European journal of pharmacology.

Taurine chloramine potentiates phagocytic activity of peritoneal macrophages through up‐regulation of dectin‐1 mediated by heme oxygenase‐1‐derived carbon monoxide

Y. Surh, Y. Suh, Kyeojin Kim, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Taurine Chloramine Stimulates Efferocytosis Through Upregulation of Nrf2-Mediated Heme Oxygenase-1 Expression in Murine Macrophages: Possible Involvement of Carbon Monoxide.

Y. Surh, Hyeon-Ok Jin, Hoon Kim, 2015, Antioxidants & redox signaling.

Combined effect of vascular-leakage-blocker Sac-1004 and antiangiogenic drug sunitinib on tumor angiogenesis.

Y. Suh, Kyeojin Kim, Young-Guen Kwon, 2014, Biochemical and biophysical research communications.

Sac-1004, a novel vascular leakage blocker, enhances endothelial barrier through the cAMP/Rac/cortactin pathway.

Y. Suh, Kyeojin Kim, Young-Guen Kwon, 2013, Biochemical and biophysical research communications.

Novel human umbilical vein endothelial cells (HUVEC)-apoptosis inhibitory phytosterol analogues: Insight into their structure-activity relationships

Jong-Wha Jung, Y. Suh, Kyeojin Kim, 2012, Archives of pharmacal research.

Fine tuning of 4,6-bisphenyl-2-(3-alkoxyanilino)pyrimidine focusing on the activity-sensitive aminoalkoxy moiety for a therapeutically useful inhibitor of receptor for advanced glycation end products (RAGE).

Jeeyeon Lee, Hyun-Ju Park, Y. Suh, 2015, Bioorganic & medicinal chemistry.

Efficient strategy for the stereoselective synthesis of 2,3-disubstituted benzo[α]quinolizidine alkaloids: concise synthesis of (−)-protoemetinol

Y. Suh, Kyeojin Kim, Hongchan An, 2015 .

Total synthesis of (-)-deguelin via an iterative pyran-ring formation strategy.

Jeeyeon Lee, Y. Suh, Seungbeom Lee, 2015, Chemical communications.

Pyrazole-5-carboxamides, novel inhibitors of receptor for advanced glycation end products (RAGE).

Hyun-Ju Park, Y. Suh, Kyeojin Kim, 2014, European journal of medicinal chemistry.

Reaction of N‐hydroxymethylsaccharin with aliphatic carboxylic acid derivatives: Synthesis of N‐acylsaccharins and N‐(saccharinylmethyl) aliphatic carboxylates

Kyeojin Kim, Yong-Jin Yoon, Sang‐Gyeong Lee, 1989 .

Glucal-conjugated sterols as novel vascular leakage blocker: structure-activity relationship focusing on the C17-side chain.

Y. Suh, Kyeojin Kim, Young-Guen Kwon, 2014, European journal of medicinal chemistry.

Heterocycle-linked phenylbenzyl amides as novel TRPV1 antagonists and their TRPV1 binding modes: constraint-induced enhancement of in vitro and in vivo activities.

Sun Choi, Jong-Wha Jung, S. Shin, 2013, Chemistry - An Asian Journal.

Protective Effects of Taurine Chloramine on Experimentally Induced Colitis: NFκB, STAT3, and Nrf2 as Potential Targets

Y. Surh, Y. Suh, Kyeojin Kim, 2021, Antioxidants.

Cholesterol-derived novel anti-apoptotic agents on the structural basis of ginsenoside Rk1.

Y. Suh, Kyeojin Kim, Young-Guen Kwon, 2010, Bioorganic & medicinal chemistry letters.

Identification of small molecule inhibitors of the STAT3 signaling pathway: Insights into their structural features and mode of action.

Jeeyeon Lee, Y. Surh, Y. Suh, 2015, Bioorganic & medicinal chemistry letters.

15‐Deoxy‐Δ12,14‐prostaglandin J2 binds and inactivates STAT3 via covalent modification of cysteine 259 in H‐Ras‐transformed human breast epithelial cells

Y. Surh, H. Na, Y. Suh, 2021, FEBS letters.

Discovery of novel potent migrastatic Thiazolo[5,4-b]pyridines targeting Lysyl-tRNA synthetase (KRS) for treatment of Cancer metastasis.

Sunghoon Kim, Y. Jeon, Y. Suh, 2021, European journal of medicinal chemistry.

15-Keto prostaglandin E2 suppresses STAT3 signaling and inhibits breast cancer cell growth and progression

Y. Surh, H. Na, Y. Suh, 2019, Redox biology.

Direct endothelial junction restoration results in significant tumor vascular normalization and metastasis inhibition in mice

S. Ha, M. Won, G. Koh, 2014, Oncotarget.

An Electrophilic Deguelin Analogue Inhibits STAT3 Signaling in H-Ras-Transformed Human Mammary Epithelial Cells: The Cysteine 259 Residue as a Potential Target

Y. Surh, Y. Suh, Seungbeom Lee, 2020, Biomedicines.

Antitumor Activity of Novel Signal Transducer and Activator of Transcription 3 Inhibitors on Retinoblastoma

Chang Sik Cho, J. H. Kim, D. Jo, 2021, Molecular Pharmacology.

Taurine chloramine potentiates phagocytic activity of peritoneal macrophages through up‐regulation of dectin‐1 mediated by heme oxygenase‐1‐derived carbon monoxide

Y. Surh, Y. Suh, Kyeojin Kim, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Anti-tumor Activity of Novel STAT3 Inhibitors on Retinoblastoma

Chang Sik Cho, J. H. Kim, D. Jo, 2021 .

Identification and Structural Analysis of New Nrf2 Activators by Mechanism‐Based Chemical Transformation of 15‐Deoxy‐Δ12, 14‐PGJ2

Jeeyeon Lee, Y. Surh, Hyun-Ju Park, 2016, Chembiochem : a European journal of chemical biology.