Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1372898 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
With bioactivity-guided phenotype screenings, a potent anti-inflammatory compound f152A1 has been isolated, characterized and identified as the known natural product LL-Z1640-2. Metabolic instability precluded its use for the study on animal disease models. Via total synthesis, a potent, metabolically stabilized analog ER-803064 has been created; addition of the (S)-Me group at C4 onto f152A1 has resulted in a dramatic improvement on its metabolic stability, while preserving the anti-inflammatory activities.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
H. Du, T. Matsushima, M. Spyvee, M. Goto, H. Shirota, F. Gusovsky, K. Chiba, M. Kotake, N. Yoneda, Y. Eguchi, L. DiPietro, J.-C. Harmange, S. Gilbert, X.-Y. Li, H. Davis, Y. Jiang, Z. Zhang, R. Pelletier, N. Wong, H. Sakurai, H. Yang, H. Ito-Igarashi,