Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10594008 | Bioorganic & Medicinal Chemistry Letters | 2011 | 5 Pages |
Abstract
Quinazolin-4-one 1 was identified as an inhibitor of the HIF-1α transcriptional factor from a high-throughput screen. HIF-1α up-regulation is common in many cancer cells. In this Letter, we describe an efficient one-pot sequential reaction for the synthesis of quinazolin-4-one 1 analogues. The structure-activity relationship (SAR) study led to the 5-fold more potent analogue, 16.
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Authors
Wenwei Huang, Ruili Huang, Matias S. Attene-Ramos, Srilatha Sakamuru, Erika E. Englund, James Inglese, Christopher P. Austin, Menghang Xia,