S. Hsieh

Synthesis of a carboxyl linker containing Pk trisaccharide.

Chien-Tien Chen, Chun-Cheng Lin, Mi-Dan Jan, 2005, Carbohydrate research.

BPR1J-097, a novel FLT3 kinase inhibitor, exerts potent inhibitory activity against AML

Y. Chao, W. Jiaang, C-W Chen, 2011, British Journal of Cancer.

Simple and efficient per-O-acetylation of carbohydrates by lithium perchlorate catalyst

Chien-Tien Chen, Chun-Cheng Lin, Kuo-Cheng Lu, 2004 .

Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3).

C. Chen, Y. Chao, J. Hsu, 2011, Bioorganic & medicinal chemistry.

3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3).

C. Chen, Y. Chao, J. Hsu, 2012, Bioorganic & medicinal chemistry letters.

Evaluation of the Antitumor Effects of BPR1J-340, a Potent and Selective FLT3 Inhibitor, Alone or in Combination with an HDAC Inhibitor, Vorinostat, in AML Cancer

C. Chen, Y. Chao, T. Yeh, 2014, PloS one.

Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3).

C. Chen, Y. Chao, J. Hsu, 2013, Bioorganic & medicinal chemistry.