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LP99 

Cat. No. M28904

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LP99  Structure

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Quality Control & Documentation
Biological Activity

LP99, an epigenetic probe, is a potent and selective inhibitor of the BRD7 and BRD9 bromodomains with a Kd of 99 nM against BRD9. LP99 disrupts the binding of BRD7 and BRD9 to chromatin in cells.

Chemical Information
Molecular Weight 516.05
Formula C26H30ClN3O4S
CAS Number 1808951-93-0
Form Solid
Solubility (25°C) DMSO 50 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Maria Mushtaq Ali, et al. Int J Biol Macromol. Epigenetic modulation by targeting bromodomain containing protein 9 (BRD9): Its therapeutic potential and selective inhibition

[2] Melanie R Müller, et al. Clin Epigenetics. Therapeutical interference with the epigenetic landscape of germ cell tumors: a comparative drug study and new mechanistical insights

[3] Peter G K Clark, et al. Angew Chem Weinheim Bergstr Ger. LP99: Discovery and Synthesis of the First Selective BRD7/9 Bromodomain Inhibitor

[4] Peter G K Clark, et al. Angew Chem Int Ed Engl. LP99: Discovery and Synthesis of the First Selective BRD7/9 Bromodomain Inhibitor

Related Epigenetic Reader Domain Products
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I-BET151

I-BET151 (GSK1210151A) is an inhibitor of the BET family with IC50 of 0.5 μM, 0.25 μM and 0.79 μM for BRD2, BRD3 and BRD4, respectively.

(+)-JQ1

(+)-JQ1 is a BET bromodomain inhibitor that acts on BRD4(2) with an IC50 of 33 nM and binds to all bromodomain domains in the BET family, but not to bromodomain domains outside the BET family. JQ1 down-regulates CD47 expression through a C-MYC-mediated pathway, and JQ1 down-regulates CD47 expression through a C-MYC-mediated pathway.

I-BET-762

I-BET-762 (GSK525762) is a selective small molecule BET inhibitor.

CPI-0610

CPI-0610 is a novel BET protein bromodomain inhibitor.

  Catalog
Abmole Inhibitor Catalog




Keywords: LP99  supplier, Epigenetic Reader Domain, inhibitors, activators

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