Szerző: " Chuang Da-Wei"

Hunyadi Attila; Martins Ana; Dankó Balázs; Chuang Da-Wei; Trouillas Patrick; Chang Fang-Rong; Wu Yang-Chang; Falkay György: Discovery of the first non-planar flavonoid that can strongly inhibit xanthine oxidase: protoapigenone 1′-O-propargyl ether.
Tetrahedron Letters, 54 (48). pp. 6529-6532. ISSN 0040-4039 (2013)

Dankó Balázs Ödön; Martins Ana; Chuang Da-Wei; Wang Hui-Chun; Amaral Leonard; Molnár József; Chang Fang-Rong; Wu Yang-Chang; Hunyadi Attila: In vitro cytotoxic activity of novel protoflavone analogs – selectivity towards a multidrug resistant cancer cell line.
Anticancer Research, 32 (7). pp. 2863-2869. ISSN 0250-7005 (2012)

Wang Hui-Chun; Lee Alan Yueh-Luen; Chou Wen-Cheng; Wu Chin-Chung; Tseng Chao-Neng; Liu Kevin Yen-Ting; Lin Wen-Lien; Chang Fang-Rong; Chuang Da-Wei; Hunyadi Attila; Wu Yang-Chang: Inhibition of ATR-dependent signaling by protoapigenone and its derivative sensitizes cancer cells to interstrand cross-link–generating agents in vitro and in vivo.
Molecular Cancer Therapeutics, 11 (7). pp. 1443-1453. ISSN 1535-7163 (2012)

Hunyadi Attila; Chuang Da-Wei; Dankó Balázs Ödön; Chiang Michael Y; Lee Chia-Lin; Wang Hui-Chun; Wu Chin-Chung; Chang Fang-Rong; Wu Yang-Chang: Direct semi-synthesis of the anticancer lead-drug protoapigenone from apigenin, and synthesis of further new cytotoxic protoflavone derivatives.
PLoS ONE, 6 (8). e23922. ISSN 1932-6203 (2011)

Tung Chao-Ping; Chang Fang-Rong; Wu Yang-Chang; Chuang Da-Wei; Hunyadi Attila; Liu Shih-Tung: Inhibition of the Epstein-Barr virus lytic cycle by protoapigenone.
Journal of General Virology, 92 (8). pp. 1760-1768. ISSN 0022-1317 (2011)