4 Results for "

NuRD complex

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "NuRD complex" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-141550
CAS No.: 2305052-86-0
Purity:  99.92%
Target:  

NF-κB

Research Areas:  

Inflammation/Immunology

BPK-25, an active acrylamide, promotes degradation of nucleosome remodeling and deacetylation (NuRD) complex proteins by a post-translational mechanism involving covalent protein engagement. BPK-25 inhibits TMEM173 activation by the cyclic dinucleotide ligand cGAMP .
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Cat. No.: HY-153358
CAS No.: 2935964-98-8
Purity:  99.91%
Target:  

HDAC

Research Areas:  

Cancer

TNG260 is a selective, orally effective inhibitor of HDAC1 and CoREST complex, with a 10-fold selectivity for HDAC1 over HDAC3 and a 500-fold selectivity for CoREST complex over NuRD and Sin3 complex. TNG260 reshapes the tumor immune microenvironment, reduces immunosuppressive neutrophil infiltration, promotes effector T cell recruitment, and reverses anti-PD-1 resistance caused by STK11 deficiency by inhibiting the activity of the CoREST-HDAC1 complex. TNG260 induces durable tumor regression in combination with α-PD1 in MC38 tumor-bearing mice with STK11 mutations, and has lower toxicity to bone marrow cells than non-selective HDAC inhibitors .
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Cat. No.: HY-179238
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

CS-1-103 is a potent estrogen receptor (ER) TRACER (transcriptional regulation via active control of epigenetic reprogramming). CS-1-103 inhibits ER transcriptional activity with an EC50 of 0.36 μM by recruiting methyl-CpG binding domain protein 2 (MBD2), HDACs and the nucleosome remodeling and deacetylase (NuRD) complex. CS-1-103 can be used for breast and prostate cancer research .
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Cat. No.: HY-128562
CAS No.: 315702-79-5
Target:  

Estrogen Receptor/ERR

Research Areas:  

Others

CS-1-69 is an MBD2 ligand analog that does not bind to individual NuRD components MBD2 or HDAC1, but binds robustly to the assembled NuRD complex (MBD2, HDAC1, and MT1A) in a dose-responsive manner. CS-1-69 attenuates Transcriptional Repression via Active Chemical Epigenetic Reprogrammin (TRACER)-mediated strogen receptor (ER) inhibitory activity .
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