K. Huang

发表

Synthesis, cytotoxicity and human telomerase inhibition activities of a series of 1,2-heteroannelated anthraquinones and anthra[1,2-d]imidazole-6,11-dione homologues.

Hsu-Shan Huang, Jing-Jer Lin, Jing-Ru Jhan, 2009, Bioorganic & medicinal chemistry.

Synthesis, antiproliferative activities and telomerase inhibition evaluation of novel asymmetrical 1,2-disubstituted amidoanthraquinone derivatives.

J. Guh, Hsu-Shan Huang, Jing-Jer Lin, 2012, European journal of medicinal chemistry.

Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents.

Hsu-Shan Huang, Jing-Jer Lin, Dah-Shyong Yu, 2013, European journal of medicinal chemistry.

Synthesis, Telomerase Evaluation and Anti‐Proliferative Studies on Various Series of Diaminoanthraquinone‐Linked Aminoacyl Residue Derivatives

Hsu-Shan Huang, Jing-Jer Lin, K. Huang, 2012, Archiv der Pharmazie.

Synthesis, human telomerase inhibition and anti-proliferative studies of a series of 2,7-bis-substituted amido-anthraquinone derivatives.

Hsu-Shan Huang, Jing-Jer Lin, Yi-Hsuan Chiang, 2008, Bioorganic & medicinal chemistry.

Synthesis and human telomerase inhibition of a series of regioisomeric disubstituted amidoanthraquinones.

Hsu-Shan Huang, Jing-Jer Lin, K. Huang, 2007, Chemical & pharmaceutical bulletin.

NSC746364, NSC746365, and NSC746366: the spectra of cytotoxicity and molecular correlates of response to telomerase activity

Hsu-Shan Huang, Jing-Jer Lin, K. Huang, 2010, Anti-cancer drugs.

Design, synthesis and evaluation of telomerase inhibitory, hTERT repressing, and anti-proliferation activities of symmetrical 1,8-disubstituted amidoanthraquinones.

D. Chang, Hsu-Shan Huang, Jing-Jer Lin, 2012, European journal of medicinal chemistry.

New Approaches of PARP-1 Inhibitors in Human Lung Cancer Cells and Cancer Stem-Like Cells by Some Selected Anthraquinone-Derived Small Molecules

S. Chiou, Hsu-Shan Huang, Dah-Shyong Yu, 2013, PloS one.

Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology.

Tsung-Chih Chen, J. Guh, D. Chang, 2013, European journal of medicinal chemistry.

Design, synthesis and antiproliferative evaluation of fluorenone analogs with DNA topoisomerase I inhibitory properties.

J. Guh, D. Chang, Hsu-Shan Huang, 2013, Bioorganic & medicinal chemistry.

Second Generation Drugs-derivatives of Natural Antitumor Anthracycline Antibiotics Daunorubicin, Doxorubicin and Carminomycin

M. Preobrazhenskaya, Hsu-Shan Huang, A. Tevyashova, 2006 .