As a member of the triazolodiazepine family (+)JQ1, it is a potent, specific and reversible pan-BET (bromodomain and exoterminal motif) family inhibitor. (+)-JQ1 may serve as a useful chemical probe to study the role of the BET bromodomain in the transcriptional regulation of tumorigenesis. (+)-JQ1 binds to BRD4 bromodomains 1 and 2 with Kd values of approximately 50 and 90 nM, respectively. This binding competes with acetyllysine.
AxisPharm offers 5000+ PEG Linkers with high purity. Different kinds of PEG Reagents may be available by custom synthesis.
![l-[(3R)-3-[4-amino-3-(4-phenoxyphenyl)-lHpyrazolo [3,4-d]pyrimidin-l-yl]-l-piperidinyl]-2-propyn-l-one](https://e1752fbe.rocketcdn.me/wp-content/uploads/AP14272-CAS-936563-91-6-1-e1686054563587.png)
