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NB512

NB512 (compound 39a) is a dual inhibitor for BET and HDAC, which exhibits a efficient binding affinity with BRD4 bromodomains and HDAC1/2, with EC50s of 100-400 nM. NB512 exhibits an anti-proliferative activity towards cancer cells PaTu8988T and NMC[1].

Product Specifications

UNSPSC

12352005

Target

Epigenetic Reader Domain; HDAC

Type

Reference compound

Related Pathways

Cell Cycle/DNA Damage; Epigenetics

Applications

Cancer-programmed cell death

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/nb512.html

Solubility

10 mM in DMSO

Smiles

O=C(NC1=CC(C2=CC=CC=C2)=CC=C1N)C3=NC=C(C4=CN(C)C(C5=C4C=CN5)=O)C=C3

Molecular Formula

C26H21N5O2

Molecular Weight

435.48

References & Citations

[1]Bauer N, et al., Development of Potent Dual BET/HDAC Inhibitors via Pharmacophore Merging and Structure-Guided Optimization. ACS Chem Biol. 2024 Feb 16;19 (2) :266-279.

Shipping Conditions

Room temperature

Product Datasheet

http://file.medchemexpress.com/batch_PDF/HY-163282/NB512-DataSheet-MedChemExpress.pdf

Product MSDS

http://file.medchemexpress.com/batch_PDF/HY-163282/

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

BRD4; HDAC1; HDAC2; HDAC3

Curated Selection

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