Antitumor Agents. 207. Design, Synthesis, and Biological Testing of 4β-Anilino-2-fluoro-4‘-demethylpodophyllotoxin Analogues as Cytotoxic and Antiviral Agents
Journal of Medicinal Chemistry2001Vol. 44(9), pp. 1422–1428
Citations Over TimeTop 19% of 2001 papers
Abstract
2-Fluoropodophyllotoxin (11) and several 4beta-anilino-2-fluoro-4'-O-demethyl analogues were synthesized and evaluated in both antineoplastic and antiviral assays. These compounds were moderately active against some cancer cell lines, but they were less active than the corresponding nonfluorinated analogues. Compound 11 exhibited the best activity against KB carcinoma with a GI(50) of approximately 30 nM. Most compounds exhibited moderate activity against HCMV with ID(50) and ID(90) values in the range of 1 microM and 4 microM, respectively. Both 9 and 11 showed an unusual 10-fold selectivity for HSV-2 compared to HSV-1.
Related Papers
- → Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines(2010)90 cited
- → Synthesis, cytotoxicity, and structure–activity relationship (SAR) studies of andrographolide analogues as anti-cancer agent(2010)62 cited
- → First Total Synthesis of Protoapigenone and Its Analogues as Potent Cytotoxic Agents(2007)58 cited
- → Cryptolepine analogues containing basic aminoalkyl side-chains at C-11: Synthesis, antiplasmodial activity, and cytotoxicity(2008)50 cited
- → Synthesis, cytotoxic activity and structure–activity relationships of hedychenone analogues(2010)22 cited