公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
1999 | Steroids used to desensitize penicillamine allergy in Wilson disease | Hsu H.-L.; Huang F.-C.; YEN-HSUAN NI ; MEI-HWEI CHANG | Acta Paediatrica Taiwanica | 5 | 0 | |
2013 | Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents | Chen T.-C.; Yu D.-S.; Huang K.-F.; Fu Y.-C.; Lee C.-C.; Chen C.-L.; Huang F.-C.; Hsieh H.-H.; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 26 | 24 | |
2013 | 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 | Chen C.-L.; Chang D.-M.; Chen T.-C.; Lee C.-C.; Hsieh H.-H.; Huang F.-C.; Huang K.-F.; JIH-HWA GUH ; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 35 | 34 | |
2009 | Synthesis and cytotoxic properties of 4,11-bis[(aminoethyl)amino]anthra[2,3-b]thiophene-5,10-diones, novel analogues of antitumor anthracene-9,10-diones | Shchekotikhin A.E.; Glazunova V.A.; Dezhenkova L.G.; Luzikov Y.N.; Sinkevich Y.B.; Kovalenko L.V.; Buyanov V.N.; Balzarini J.; Huang F.-C.; JING-JER LIN ; Huang H.-S.; Shtil A.A.; Preobrazhenskaya M.N. | Bioorganic and Medicinal Chemistry | 42 | 37 | |
2007 | Synthesis and human telomerase inhibition of a series of regioisomeric disubstituted amidoanthraquinones | Huang H.-S.; Chen I.-B.; Huang K.-F.; Lu W.-C.; Shieh F.-Y.; Huang Y.-Y.; Huang F.-C.; JING-JER LIN | Chemical and Pharmaceutical Bulletin | 48 | 44 | |
2012 | Synthesis, antiproliferative activities and telomerase inhibition evaluation of novel asymmetrical 1,2-disubstituted amidoanthraquinone derivatives | Lee C.-C.; Huang K.-F.; Lin P.-Y.; Huang F.-C.; Chen C.-L.; Chen T.-C.; JIH-HWA GUH ; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 27 | 23 | |
2009 | 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 | Huang H.-S.; Chen T.-C.; Chen R.-H.; Huang K.-F.; Huang F.-C.; Jhan J.-R.; Chen C.-L.; Lee C.-C.; Lo Y.; JING-JER LIN | Bioorganic and Medicinal Chemistry | 56 | 51 | |
2008 | Synthesis, human telomerase inhibition and anti-proliferative studies of a series of 2,7-bis-substituted amido-anthraquinone derivatives | Huang H.-S.; Huang K.-F.; Li C.-L.; Huang Y.-Y.; Chiang Y.-H.; Huang F.-C.; JING-JER LIN | Bioorganic and Medicinal Chemistry | 48 | 41 | |
2012 | Synthesis, telomerase evaluation and anti-proliferative studies on various series of diaminoanthraquinone-lkinked aminoacyl residue derivatives | Huang F.-C.; Huang K.-F.; Chen R.-H.; Wu J.-E.; Chen T.-C.; Chen C.-L.; Lee C.-C.; Chen J.-Y.; JING-JER LIN ; Huang H.-S. | Archiv der Pharmazie | 8 | 8 | |