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

Synthesis of Unsymmetrical Biphenyls as Potent Cytotoxic Agents

Por Wu, Gang, Guo, Huan-Fang, Gao, Kun, Liu, Yi-Nan, Bastow, Kenneth F., Morris-Natschke, Susan L., Lee, Kuo-Hsiung, Xie, Lan
Publicado em 2008

Synthesis of new 2′-deoxy-2′-fluoro-4′-azido nucleoside analogues as potent anti-HIV agents

Por Wang, Qiang, Hu, Weidong, Wang, Shuyang, Pan, Zhenliang, Tao, Le, Guo, Xiaohe, Qian, Keduo, Chen, Chin-Ho, Lee, Kuo-Hsiung, Chang, Junbiao
Publicado em 2011

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)

Development and Preclinical Studies of Broad-spectrum Anti-HIV Agent (3′R,4′R)-3-Cyanomethyl-4-methyl-3′,4′-di-O-(S)-camphanoyl-(+)-cis-khellactone (3-Cyanomethyl-4-methyl-DCK)...

Por Xie, Lan, Guo, Huan-Fang, Lu, Hong, Zhuang, Xiao-Mei, Zhang, An-Ming, Wu, Gang, Ruan, Jin-Xiu, Zhou, Ting, Yu, Donglei, Qian, Keduo, Lee, Kuo-Hsiung, Jiang, Shibo
Publicado em 2008

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

Melanoma targeting property of a Lu-177-labeled lactam bridge-cyclized alpha-MSH peptide

Por Guo, Haixun, Miao, Yubin
Publicado em 2013

Synthesis and evaluation of a ligand targeting the μ and δ opioid receptors for drug delivery to lung cancer

Por Li, Guo, Low, Philip S.
Publicado no Bioorg Med Chem Lett (2016)

Substrate Modulus Regulates Osteogenic Differentiation of Rat Mesenchymal Stem Cells through Integrin β1 and BMP Receptor Type IA

Por Guo, R., Lu, S., Merkel, A. R., Sterling, J.A., Guelcher, S.A.
Publicado no J Mater Chem B Mater Biol Med (2016)

Self-assembled micelles of amphiphilic PEGylated rapamycin for loading paclitaxel and resisting multidrug resistant cancer cells

Por Tian, Wei, Liu, Jieying, Guo, Yuan, Shen, Yuanyuan, Zhou, Dejian, Guo, Shengrong
Publicado no J Mater Chem B Mater Biol Med (2015)

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