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BRD4-BD1/2-IN-3

BRD4-BD1/2-IN-3 (Compound B6) is a selective BRD4 BD2 inhibitor with an IC50 of 0.41 nM for BRD4 BD2 over BRD4 BD1. BRD4-BD1/2-IN-3 significantly inhibits the LPS (HY-D1056) -induced expression of IL-6. BRD4-BD1/2-IN-3 shows anti-inflammatory activities by modulating the TNF and NF-κB signaling pathway. BRD4-BD1/2-IN-3 can be used for inflammatory diseases research[1].

Product Specifications

UNSPSC

12352005

Target

C-Fms; Epigenetic Reader Domain; Interleukin Related; NF-κB; TNF Receptor

Related Pathways

Apoptosis; Epigenetics; Immunology/Inflammation; NF-κB; Protein Tyrosine Kinase/RTK

Field of Research

Inflammation/Immunology

Purity

99.52

Solubility

DMSO : 8.33 mg/mL (ultrasonic)

Smiles

O=C1NC(C2=CN(N=C2)CC3=CC=CC=C3)=NC4=CC(OC)=CC(OC)=C41

Molecular Formula

C20H18N4O3

Molecular Weight

362.38

References & Citations

[1]Chen S, et al. Discovery of 2- (Pyrazol-4-yl) -quinazolin-4 (3H) -one Derivatives as Subnanomolar BRD4 BD2 Inhibitors with High Selectivity via a Bioisosterism Approach. J Med Chem. 2025 Sep 11;68 (17) :18314-18334.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Product MSDS

http://file.medchemexpress.com/batch_PDF/HY-178041/BRD4-BD1-2-IN-3-SDS-MedChemExpress.pdf

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

BD1; BD2; IL-1; IL-6; RelA/p65

Available Sizes

Curated Selection

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