Zobrazeno 1 - 5 of 5 pro vyhledávání: '"Hong bin Yoon"'
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Abstract LB524: Discovery of highly selective RON kinase inhibitors
Autor: Young Jin Ham, GyeongHwan Kim, Juhyun Lee, Jaeyoung Lee, Min Kyung Kim, Sunhong Kim, Woosook Kim, Han Byoul Kim, Sung Woong Jang, Hee Dong Park, Seonguk Jeon, Seok-Joo Kim, Joongheui Cho, Jungjoon Kim, Hong bin Yoon, Youngshin Kwak
Publikováno v: Cancer Research. 82:LB524-LB524
RON is a receptor tyrosine kinase of the MET proto-oncogene family, known as macrophage stimulating 1 receptor (MST1R) that recognizes macrophage-stimulating protein (MSP). RON has been known to be highly expressed in several epithelial tumors, promo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::87432313cc8d8e46033f06bb9f89c11c
https://doi.org/10.1158/1538-7445.am2022-lb524
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3
Michael Addition of Thiol Compounds on ω-Maleate Poly(ethylene oxide)s: Model Study for the 'Site-Specific' Modification of Proteins
Autor: Jeewoo Lim, Jungahn Kim, Hong Bin Yoon, Youra Lee, Abu Bakkar Siddique, Jae Yeol Lee, Donghwa Seo, Saeon Kim
Publikováno v: Macromolecular Research. 26:194-203
In this study, we successfully synthesized ω-maleate poly(ethylene oxide)s (PEOs) as the modifier for proteins through the thiol-ene Michael addition reaction. Both α-azido-ω-maleate PEO and α-t-butoxy-ω-maleate PEO were obtained from the reacti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c6b2a583d3cd61cf370282558284b868
https://doi.org/10.1007/s13233-018-6021-4
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4
Synthesis and biological evaluation of fluoro-substituted 3,4-dihydroquinazoline derivatives for cytotoxic and analgesic effects
Autor: Vinicius M. Gadotti, Hui Rak Jeong, Jin Han Kim, Sun Young Kim, Fang-Xiong Zhang, Da Woon Jung, Jae Yeol Lee, Hyoung Ja Kim, Kyung-Tae Lee, Hong Bin Yoon, Junting Huang, Gerald W. Zamponi
Publikováno v: Bioorganic & Medicinal Chemistry. 25:4656-4664
As a bioisosteric strategy to overcome the poor metabolic stability of lead compound KYS05090S, a series of new fluoro-substituted 3,4-dihydroquinazoline derivatives was prepared and evaluated for T-type calcium channel (Cav3.2) block, cytotoxic effe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f9dd3a1c1d50ea6cb681805d7cc4d4f
https://doi.org/10.1016/j.bmc.2017.07.010
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Plný text Recenzováno Digitální knihovna AV ČR
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