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DCZ0415

Cat. No. M14600

All AbMole products are for research use only, cannot be used for human consumption.

DCZ0415 Structure
Size Price Availability Quantity
5mg USD 143  USD143 In stock
10mg USD 240  USD240 In stock
25mg USD 500  USD500 In stock
50mg USD 850  USD850 In stock
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Quality Control & Documentation
Biological Activity

DCZ0415, a potent TRIP13 inhibitor, impairs nonhomologous end joining repair and inhibits NF-κB activity. DCZ0415 induces anti-myeloma activity in vitro, in vivo, and in primary cells derived from drug-resistant myeloma patients.

Chemical Information
Molecular Weight 356.42
CAS Number 2242470-43-3
Solubility (25°C) DMSO 62.5 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Haojun Xu, et al. Inducing Synergistic DNA Damage by TRIP13 and PARP1 Inhibitors Provides a Potential Treatment for Hepatocellular Carcinoma

[2] Sumit Agarwal, et al. DCZ0415, a small-molecule inhibitor targeting TRIP13, inhibits EMT and metastasis via inactivation of the FGFR4/STAT3 axis and the Wnt/β-catenin pathway in colorectal cancer

[3] Yan Chen, et al. TRIP13, identified as a hub gene of tumor progression, is the target of microRNA-4693-5p and a potential therapeutic target for colorectal cancer

[4] Yingcong Wang, et al. A Small-Molecule Inhibitor Targeting TRIP13 Suppresses Multiple Myeloma Progression

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Keywords: DCZ0415 supplier, NF-κB, inhibitors, activators

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