I-BRD9
Chemical Name: 5-Ethyl-4,5-dihydro-4-oxo-N-(tetrahydro-1,1-dioxido-2H-thiopyran-4-yl)-7-[3-(trifluoromethyl)phenyl]thieno[3,2-c]pyridine-2-carboximidamide
Purity: ≥98%
Biological Activity
I-BRD9 is a potent and selective BRD9 inhibitor (pIC50 = 7.3). Exhibits >70-fold selectivity for BRD9 over a panel of 34 other bromodomains and >700-fold selectivity over the BET family. Downregulates CLEC1, DUSP6, FES and SAMSN1 genes in Kasumi-1 cells.External Portal Information
Chemicalprobes.org is a portal that offers independent guidance on the selection and/or application of small molecules for research. The use of I-BRD9 is reviewed on the chemical probes website.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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Discovery of I-BRD9, a selective cell active chemical probe for bromodomain containing protein 9 inhibition.
Theodoulou et al.
J.Med.Chem, 2015;59:1425
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Citations for I-BRD9
The citations listed below are publications that use Tocris products. Selected citations for I-BRD9 include:
5 Citations: Showing 1 - 5
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BRD9-mediated chromatin remodeling suppresses osteoclastogenesis through negative feedback mechanism.
Authors: Yili Et al.
Nat Commun 2023;14:1413
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BRD9 regulates interferon-stimulated genes during macrophage activation via cooperation with BET protein BRD4.
Authors: Nasun Et al.
Proc Natl Acad Sci U S A 2022;119
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The bromodomain containing protein BRD-9 orchestrates RAD51-RAD54 complex formation and regulates homologous recombination-mediated repair.
Authors: Yong Et al.
Nat Commun 2020;11:2639
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Targeted degradation of BRD9 reverses oncogenic gene expression in synovial sarcoma.
Authors: Brien Et al.
Elife 2018;7:e41305
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Vitamin D switches BAF complexes to protect β cells.
Authors: Wei Et al.
Cell 2018;173:1135
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