Synthesis and SAR study of prenylated xanthone analogues as HeLa and MDA-MB-231 cancer cell inhibitors

Letters in Drug Design and Discovery

Volumn 8, Issue 6, 2011, Pages 523-528

  Lim, Chan Kiang ^a   Tho, Lai Yeng ^a   Lim, Cheng Hoe ^a   Lim, Yang Mooi ^a   Shah, Syed Adnan Ali ^b   Weber, Jean Frederic Faizal ^b  

^a UNIVERSITI TUNKU ABDUL RAHMAN   (Malaysia)

^b UNIVERSITI TEKNOLOGI MARA   (Malaysia)

Author keywords

2H xanthene 3,6,9(7H) trione scaffold; 2H xanthene 3,9 dione scaffold; Cytotoxicity; Inhibitory activity; Synthesis; Xanthone derivatives

Indexed keywords

2H XANTHENE 3,9 DIONE; ANTINEOPLASTIC AGENT; CISPLATIN; DOXORUBICIN; MOLECULAR SCAFFOLD; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

ARTICLE; CANCER INHIBITION; CYTOTOXICITY; DRUG STRUCTURE; DRUG SYNTHESIS; HELA CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; INHIBITION KINETICS; POSITION EFFECT; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION;

EID: 79959333064     PISSN: 15701808     EISSN: 1875628X     Source Type: Journal    
DOI: 10.2174/157018011795906820     Document Type: Article

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