Top Suppliers:I want be here

  • DC Chemicals Limited
  • China
  • Product Name: CEP-9722
  • Price: $Inquiry/100mg ¥Inquiry/250mg ¥Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 1 Day
  • Contact: Tony Cao

916574-83-9

916574-83-9 structure
916574-83-9 structure
  • Name: CEP-9722
  • Chemical Name: CEP-9722
  • CAS Number: 916574-83-9
  • Molecular Formula: C24H26N4O3
  • Molecular Weight: 418.49
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage PARP
  • Create Date: 2022-01-08 21:46:59
  • Modify Date: 2024-01-10 16:16:40
  • CEP-9722, the prodrug of CEP-8983, is a selective and orally active PARP-1 and PARP-2 inhibitor with IC50s of 20 nM and 6 nM, respectively. CEP-9722 has anticancer effects[1][2].

Name CEP-9722
Description CEP-9722, the prodrug of CEP-8983, is a selective and orally active PARP-1 and PARP-2 inhibitor with IC50s of 20 nM and 6 nM, respectively. CEP-9722 has anticancer effects[1][2].
Related Catalog
Target

PARP-1:20 nM (IC50)

PARP-2:6 nM (IC50)

In Vivo CEP-9722 (100-200 mg/kg/day; oral gavage; once daily; for 5 days a week for 4 weeks) shows dose-dependent antitumor activity in RT4 xenografts; 200 mg/kg daily is better than control and 100 mg/kg is not[1]. Animal Model: Nude mice bearing subcutaneous RT4 human urothelial carcinoma (UC) tumors[1] Dosage: 100 or 200 mg/kg/day Administration: Oral gavage; once daily; for 5 days a week for 4 weeks Result: Showed dose-dependent antitumor activity in RT4 xenografts.
References

[1]. Weiguo Jian, et al. Activity of CEP-9722, a poly (ADP-ribose) polymerase inhibitor, in urothelial carcinoma correlates inversely with homologous recombination repair response to DNA damage. Anticancer Drugs. 2014 Sep;25(8):878-86.

[2]. Ruth Plummer, et al. Phase 1 dose-escalation study of the PARP inhibitor CEP-9722 as monotherapy or in combination with temozolomide in patients with solid tumors. Cancer Chemother Pharmacol. 2014 Aug;74(2):257-65.

Molecular Formula C24H26N4O3
Molecular Weight 418.49