| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1362948 | Bioorganic & Medicinal Chemistry Letters | 2010 | 5 Pages |
Abstract
The amino-epoxyquinols 6a and 6b were synthesized as soluble derivatives of an NF-κB inhibitor DHMEQ (1). In spite of the opposite configuration from 1, 6b rather than 6a affected the deactivation of NF-κB, based on NO secretion and MALDI-TOF MS analysis. It was indicated that 6b inhibited the activation by different manner from that of 1.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tsuyoshi Saitoh, Chika Shimada, Masatoshi Takeiri, Mitsuhiro Shiino, Shigeru Ohba, Rika Obata, Yuichi Ishikawa, Kazuo Umezawa, Shigeru Nishiyama,