Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1357166 | Bioorganic & Medicinal Chemistry | 2005 | 6 Pages |
Abstract
Several new phorbol derivatives having ethereal substituents at the 12-position were synthesized and subjected to biological evaluation to find new candidates of an anti-HIV agent. Among them, 12-O-(methoxymethyl)phorbol 13-decanoate showed potent inhibitory activity against infection of HIV-1 in MT-4 cells (EC50: 1.3 ng/mL) and relatively low cytotoxicity (CC50: 8.3 μg/mL). This compound was also found to have sufficient stability in mouse plasma compared with the corresponding 12-acetate derivative, which was an equipotent HIV-1 inhibitor, but with an activity that decreased considerably after plasma treatment.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yuji Matsuya, Zhong Yu, Naoki Yamamoto, Masao Mori, Haruo Saito, Makoto Takeuchi, Mamiko Ito, Hideo Nemoto,