This research was supported in part by the National Institutes of Health (NS059478-01) and Accelerate Brain Cancer Cure. D.D.Y. acknowledges a graduate research fellowship from the ACS Medicinal Chemistry Division. A.D. is a Beckman Young Investigator and a Cottrell Scholar. Q.H. acknowledges support from the Elsa Pardee Foundation, Breast Cancer Alliance, and the V Foundation.
Communication
Small-Molecule Inhibitors of MicroRNA miR-21 Function†
Article first published online: 19 AUG 2008
DOI: 10.1002/anie.200801555
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Angewandte Chemie International Edition
Volume 47, Issue 39, pages 7482–7484, September 15, 2008
Additional Information
How to Cite
Gumireddy, K., Young, Douglas D., Xiong, X., Hogenesch, John B., Huang, Q. and Deiters, A. (2008), Small-Molecule Inhibitors of MicroRNA miR-21 Function. Angew. Chem. Int. Ed., 47: 7482–7484. doi: 10.1002/anie.200801555
- †
Publication History
- Issue published online: 9 SEP 2008
- Article first published online: 19 AUG 2008
- Manuscript Revised: 20 JUN 2008
- Manuscript Received: 3 APR 2008
Funded by
- National Institutes of Health. Grant Number: NS059478-01
- Accelerate Brain Cancer Cure
- ACS Medicinal Chemistry Division
- Elsa Pardee Foundation
- Breast Cancer Alliance
- V Foundation
Keywords:
- antitumor agents;
- cell-based assays;
- inhibitors;
- medicinal chemistry;
- microRNA

Short, but significant, microRNAs (miRNAs) are an important class of gene regulators. Small-molecule modifiers of miRNA function, such as 1 (see schematic representation), were identified in a cellular screen for miRNA-pathway inhibitors. Such compounds are expected to be useful tools for the elucidation of detailed mechanisms of miRNA action and may serve as lead structures for the development of new therapeutic agents.

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