Alkyl and carboxylalkyl esters of 4'-demethyl-4-deoxypodophyllotoxin: synthesis, cytotoxic, and antitumor activity.
Young-Jae You, Yong Kim, Nguyen-Hai Nam, Seong-Cheol Bang, Byung-Zun Ahn
Index: Eur. J. Med. Chem. 39(2) , 189-93, (2004)
Full Text: HTML
Abstract
Esters of 4'-demethyl-4-deoxypodophyllotoxin (DDPT) with alkanoic acids and alkanedioic acids were prepared and tested for cytotoxic and antitumor activity. Among 19 esters, esters of propanoic acid, tetradecanedioic acid, 13-carboxyundecanoic acid, and hexadecanedioic acid improved the antitumor activity compared with that of the starting compounds, DDPT.
Related Compounds
Related Articles:
2014-07-03
[J. Proteome Res. 13(7) , 3444-54, (2014)]
1989-11-01
[J. Lipid Res. 30(11) , 1711-8, (1989)]
Subcellular localization of hexadecanedioic acid activation in human liver.
1974-11-01
[J. Lipid Res. 15(6) , 551-6, (1974)]
1993-12-14
[Biochemistry 32(49) , 13732-41, (1993)]
Hexadecanedionic acid-sepharose 4B: A new tool for preparation of albumin-depleted plasma.
2006-12-01
[J. Proteome Res. 5(12) , 3453-8, (2006)]