5 Results for "

ATAD2 Inhibitors

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "ATAD2 Inhibitors" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-119254
CAS No.: 2099142-76-2
Purity:  98.33%
Research Areas:  

Metabolic Disease

BAY-850, a chemical probe, is a potent and isoform selective ATPase family AAA domain-containing protein 2 (ATAD2) inhibitor, with an IC50 of 166 nM .
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1
1 Cited Publications
Cat. No.: HY-114204
CAS No.: 1997369-78-4
Purity:  99.80%
Research Areas:  

Cancer

GSK8814 is a potent and selective ATAD2 bromodomain chemical probe and inhibitor (IC50 = 0.059 μM), with a binding constant pKd = 8.1 and a pKi = 8.9 in BROMOscan. GSK8814 binds to ATAD2 and BRD4 BD1 with pIC50s of 7.3 and 4.6, respectively. GSK8814 shows 500-fold selectivity for ATAD2 over BRD4 BD1. GSK8814 can be researched for cancer associated with ATAD2 bromodomain .
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Cat. No.: HY-136521
CAS No.: 3040082-19-4
Purity:  99.22%
Research Areas:  

Cancer

AZ13824374 is a potent and selective ATAD2 bromodomain inhibitor (pIC50 of 6.9 in HCT116 cells). AZ13824374 disrupts chromatin interactions and gene transcription by binding to the acetyl-lysine binding site of the ATAD2 bromodomain. AZ13824374 has anticancer activity against breast cancer .
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Cat. No.: HY-119254A
Purity:  98.12%
Research Areas:  

Metabolic Disease

trans-BAY-850 is the trans isomer of BAY-850 (HY-119254). BAY-850 is a potent and isoform selective ATPase family AAA domain-containing protein 2 (ATAD2) inhibitor, with an IC50 of 166 nM.
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Cat. No.: HY-163108
CAS No.: 3004556-06-0
Research Areas:  

Cancer

ATAD2-IN-1 (compound 19f) is a potent ATAD2 inhibitor (IC50: 0.27 μM) and can induce apoptosis. ATAD2-IN-1 also inhibits c-Myc activation and BT-549 cell migration .
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