Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376315 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
A series of novel diaryl ethers possessing various functional groups were synthesized and evaluated for antiproliferative activity in human myeloid leukemia HL-60 cells. Among the compounds examined, compounds 10, 17, 20, 24, and 33 showed moderate to potent antiproliferative activity. These derivatives were further examined in terms of their abilities to inhibit tubulin polymerization; however, all of the tested compounds were relatively ineffective. The reference compound E7010 with an IC50 of 0.34 μM exhibited potent antiproliferative activity and significantly inhibited tubulin polymerization in a dose-dependent manner.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jin-Kyung In, Mi-Sung Lee, Jung-Eun Yang, Jae-Hwan Kwak, Heesoon Lee, Shanthaveerappa K. Boovanahalli, Kyeong Lee, Soo Jin Kim, Seung Kee Moon, Sungsook Lee, Nam Song Choi, Soon Kil Ahn, Jae-Kyung Jung,