(+)-JQ1 PA
Chemical Name: (6S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-N-2-propyn-1-yl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetamide
Purity: ≥95%
Biological Activity
(+)-JQ1 PA is a click-activated (alkyne) version of the BET bromodomain inhibitor (+)-JQ1 (Cat. No. 4499). Can be used as a precursor to a PROTAC® targeting BET bromodomains. Supplied with an alkyne functionalized handle for click conjugation to a linker/E3 ligase ligand. Can also be conjugated to fluorescent dyes for imaging aplications.PROTAC® is a registered trademark of Arvinas Operations, Inc., and is used under license.
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.
Background References
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Click chemistry enables preclinical evaluation of targeted epigenetic therapies.
Tyler et al.
Science, 2017;356:1397
Product Datasheets
Citation for (+)-JQ1 PA
The citations listed below are publications that use Tocris products. Selected citations for (+)-JQ1 PA include:
1 Citation: Showing 1 - 1
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Small molecule JQ1 promotes prostate cancer invasion via BET-independent inactivation of FOXA1.
Authors: Sophia Y Et al.
J Clin Invest 2020;130:1782-1792
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