| Product Name | CX-5461 | Pidnarulex | 
|---|---|
| CAS | 1138549-36-6 | 
| Formula | C27H27N7O2S | 
| MW | 513.61 | 
| Appearance | White to yellow powder | 
| Storage condition | Dry, dark and at 0 - 4 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years). | 
| Size | Availability | Price(USD) | VIP Price (USD) | Quantity | 
|---|---|---|---|---|
| 2 mg | 3-5days | ¥288.00 | Visible after login | |
| 5 mg | 3-5days | ¥498.00 | Visible after login | |
| 10 mg | 3-5days | ¥898.00 | Visible after login | |
| 25 mg | 3-5days | ¥1616.00 | Visible after login | 
| Product Name | CX-5461 | Pidnarulex | 
|---|---|
| CAS | 1138549-36-6 | 
| Formula | C27H27N7O2S | 
| MW | 513.61 | 
| Appearance | White to yellow powder | 
| Storage condition | Dry, dark and at 0 - 4 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years). | 
CX-5461 is a first-in-class non-genotoxic small molecule targeted inhibitor of RNA polymerase I (Pol I) that activates the p53 pathway without causing DNA damage. CX-5461 selectively inhibits rRNA synthesis by Pol I in the nucleolus, but does not inhibit mRNA synthesis by RNA Polymerase II (Pol II) and does not inhibit DNA replication or protein synthesis. Inhibition of Pol I results in nucleolar stress and release of ribosomal proteins (RP) from the nucleolus. The RP bind to Mdm2 and liberate p53 to orchestrate apoptosis in cancer cells. CX-5461 demonstrates a favorable preclinical profile, potently and selectively kills cancer cells, demonstrates robust in vivo efficacy in multiple models, and has demonstrated oral bioavailability in multiple species.
PMID: 21159662 DOI: 10.1158/0008-5472.CAN-10-1728
PMID: 22789538 PMCID: PMC3749732 DOI: 10.1016/j.ccr.2012.05.019