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

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

Synthesis and SAR of Thiazolylmethylphenyl Glucoside as Novel C-Aryl Glucoside SGLT2 Inhibitors

Por Song, Kwang-Seop, Lee, Suk Ho, Kim, Min Ju, Seo, Hee Jeong, Lee, Junwon, Lee, Sung-Han, Jung, Myung Eun, Son, Eun-Jung, Lee, MinWoo, Kim, Jeongmin, Lee, Jinhwa
Publicado em 2010

OGA inhibition by GlcNAc-selenazoline

Por Kim, Eun Ju, Love, Dona C., Darout, Etzer, Abdo, Mohannad, Rempel, Brian, Withers, Stephen G., Rablen, Paul R., Hanover, John A., Knapp, Spencer
Publicado em 2010

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

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)

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

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)

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

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

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)

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

Cancer Preventive Agents 9. Betulinic Acid Derivatives as Potent Cancer Chemopreventive Agents (†)

Por Nakagawa-Goto, Kyoko, Yamada, Koji, Taniguchi, Masahiko, Tokuda, Harukuni, Lee, Kuo-Hsiung
Publicado em 2009

Anti-AIDS agents 89. Identification of DCX derivatives as anti-HIV and chemosensitizing dual function agents to overcome P-gp-mediated drug resistance for AIDS therapy

Por Zhou, Ting, Ohkoshi, Emika, Shi, Qian, Bastow, Kenneth F., Lee, Kuo-Hsiung
Publicado em 2012

Structural and bioactive studies of terpenes and cyclopeptides from the Genus Rubia

Por Xu, Kuo, Wang, Penglong, Yuan, Bin, Cheng, Yatao, Li, Qiang, Lei, Haimin
Publicado em 2013

Synthesis and structure-activity relationship studies of novel 3,9-substituted α-carboline derivatives with high cytotoxic activity against colorectal cancer cells

Por Lin, Yi-Chien, Chen, Yi-Fong, Tseng, Li-Shin, Lee, Yueh-Hsuan, Morris-Natschke, Susan L, Kuo, Sheng-Chu, Yang, Ning-Sun, Lee, Kuo-Hsiung, Huang, Li-Jiau
Publicado no Eur J Med Chem (2016)

Novel Curcumin Analogs to Overcome EGFR-TKI Lung Adenocarcinoma Drug Resistance and Reduce EGFR-TKI-induced GI Adverse Effects

Por Wada, Koji, Lee, Jen-Yi, Hung, Hsin-Yi, Shi, Qian, Lin, Li, Zhao, Yu, Goto, Masuo, Yang, Pan-Chyr, Kuo, Sheng-Chu, Chen, Hui-Wen, Lee, Kuo-Hsiung
Publicado no Bioorg Med Chem (2015)

Ortho-Quinone tanshinones directly inhibit telomerase through an oxidative mechanism mediated by hydrogen peroxide

Por Soares, Joana, Keppler, Brian R., Wang, Xihong, Lee, Kuo-Hsiung, Jarstfer, Michael B.
Publicado em 2011