Inhibition of atherosclerosis-promoting microRNAs via targeted polyelectrolyte complex micelles

Por Kuo, Cheng-Hsiang, Leon, Lorraine, Chung, Eun Ji, Huang, Ru-Ting, Sontag, Timothy J., Reardon, Catherine A., Getz, Godfrey S., Tirrell, Matthew, Fang, Yun
Publicado no J Mater Chem B Mater Biol Med (2014)

Tat-DJ-1 inhibits oxidative stress-mediated RINm5F cell death through suppression of NF-κB and MAPK activation

Por Jo, Hyo Sang, Cha, Hyun Ju, Kim, Sang Jin, Yeo, Hyeon Ji, Cho, Su Bin, Park, Jung Hwan, Lee, Chi Hern, Yeo, Eun Ji, Choi, Yeon Joo, Eum, Won Sik, Choi, Soo Young
Publicado no Med Chem Res (2016)

Anti-AIDS Agents 81. Design, Synthesis and Structure-Activity Relationship Study of Betulinic Acid and Moronic Acid Derivatives as Potent HIV Maturation Inhibitors

Por Qian, Keduo, Kuo, Reen-Yun, Chen, Chin-Ho, Huang, Li, Morris-Natschke, Susan L., Lee, Kuo-Hsiung
Publicado em 2010

Syntheses and in vitro evaluation of new S1PR1 compounds and initial evaluation of a lead F-18 radiotracer in rodents

Por Luo, Zonghua, Rosenberg, Adam J., Liu, Hui, Han, Junbin, Tu, Zhude
Publicado no Eur J Med Chem (2018)

Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria

Por Shi, Li-Shian, Kuo, Sheng-Chu, Sun, Han-Dong, Morris-Natschke, Susan L., Lee, Kuo-Hsiung, Wu, Tian-Shung
Publicado no Bioorg Med Chem (2014)

Use of Ionically Tagged Glycosyl Donors in the Synthesis of Oligosaccharide Libraries

Por Kim, Eun Ju, Gray, Gary R.
Publicado em 2009

Epigenetic Modification of Histone 3 Lysine 27: MEDIATOR SUBUNIT MED25 IS REQUIRED...

Por Englert, Neal A., Luo, George, Goldstein, Joyce A., Surapureddi, Sailesh
Publicado no J Biol Chem (2015)

Simultaneous determination of methylcarbamate and ethylcarbamate in fermented foods and beverages by derivatization and GC-MS analysis

Por Shin, Ho-Sang, Yang, Eun-Young
Publicado em 2012

Design and synthesis of 6,7-methylenedioxy-4-substituted phenylquinolin-2(1H)-one derivatives as novel anticancer agents that induce apoptosis with cell cycle arrest at G2/M phase

Por Chen, Yi-Fong, Lin, Yi-Chien, Huang, Po-Kai, Chan, Hsu-Chin, Kuo, Sheng-Chu, Lee, Kuo-Hsiung, Huang, Li-Jiau
Publicado em 2013

Erratum to “Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors” [Bioorg. Med. Chem. 24 (2016) 3083...

Por Wang, Sheng-Biao, Cui, Mu-Tian, Wang, Xiao-Feng, Ohkoshi, Emika, Goto, Masuo, Yang, De-Xuan, Li, Linna, Yuan, Shoujun, Morris-Natschke, Susan L., Lee, Kuo-Hsiung, Xie, Lan
Publicado no Bioorg Med Chem (2017)

Effect of structural modification in the amine portion of substituted aminobutyl-benzamides as ligands for binding σ(1) and σ(2) receptors

Por Fan, Kuo-Hsien, Lever, John R., Lever, Susan Z.
Publicado em 2011

Structure Activity Relationships of 1,4-Dihydropyridines That Act as Enhancers of the Vanilloid Receptor 1 (TRPV1)

Por Roh, Eun Joo, Keller, Jason M., Olah, Zoltan, Iadarola, Michael J., Jacobson, Kenneth A.
Publicado em 2008

Synthesis and antitumor activity of bis(hydroxymethyl)propionate analogs of pterostilbene in cisplatin-resistant human oral cancer cells

Por Hsieh, Min-Tsang, Huang, Li-Jiau, Wu, Tian-Shung, Lin, Hui-Yi, Morris-Natschke, Susan L., Lee, Kuo-Hsiung, Kuo, Sheng-Chu
Publicado no Bioorg Med Chem (2018)

Identification of BRAF inhibitors through in silico screening

Por Luo, Cheng, Xie, Peng, Marmorstein, Ronen
Publicado em 2008

Antitumor Agents 286. Design, Synthesis and Structure-Activity Relationships of 3′R,4′R-Disubstituted-2′,2′-dimethyldihydropyrano[2,3-f]chromone (DSP) Analogs as Potent Chemosensit...

Por Zhou, Ting, Shi, Qian, Bastow, Kenneth F., Lee, Kuo-Hsiung
Publicado em 2010

Profiling Protein Arginine Deiminase 4 (PAD4): A novel screen to identify PAD4 inhibitors

Por Knuckley, Bryan, Luo, Yuan, Thompson, Paul R.
Publicado em 2007

α-Conotoxin [S9A]TxID Potently discriminates between α3β4 and α6/α3β4 Nicotinic Acetylcholine Receptors

Por Wu, Yong, Zhangsun, Dongting, Zhu, Xiaopeng, Kaas, Quentin, Zhangsun, Manqi, Harvey, Peta J., Craik, David J., McIntosh, J. Michael, Luo, Sulan
Publicado no J Med Chem (2017)

Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one Analogs as Potent Antitumor Agents that Inhibit Tubulin Assembly

Por Chang, Yu-Hsun, Hsu, Mei-Hua, Wang, Sheng-Hung, Huang, Li-Jiau, Qian, Keduo, Morris-Natschke, Susan L., Hamel, Ernest, Kuo, Sheng-Chu, Lee, Kuo-Hsiung
Publicado em 2009

Design, synthesis, and mechanism of action of 2-(3-hydroxy-5-methoxyphenyl)-6-pyrrolidinylquinolin-4-one as a potent anticancer lead

Por Cheng, Yung-Yi, Liu, Chin-Yu, Tsai, Meng-Tung, Lin, Hui-Yi, Yang, Jai-Sing, Wu, Tian-Shung, Kuo, Sheng-Chu, Huang, Li-Jiau, Lee, Kuo-Hsiung
Publicado em 2013

Synthesis and β-amyloid binding properties of rhenium 2-phenylbenzothiazoles

Por Lin, Kuo-Shyan, Debnath, Manik L., Mathis, Chester A., Klunk, William E.
Publicado em 2009