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  • DC Chemicals Limited
  • China
  • Product Name: RRx-001
  • Price: $450.0/100mg $780.0/250mg $1600.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

925206-65-1

925206-65-1 structure
925206-65-1 structure
  • Name: RRx-001
  • Chemical Name: 2-bromo-1-(3,3-dinitroazetidin-1-yl)ethanone
  • CAS Number: 925206-65-1
  • Molecular Formula: C5H6BrN3O5
  • Molecular Weight: 268.02200
  • Catalog: Signaling Pathways Anti-infection Parasite
  • Create Date: 2016-06-01 11:45:44
  • Modify Date: 2024-01-02 16:05:16
  • RRx-001 is a potent inhibitor of G6PD. RRx-001 shows potent antimalarial, although as a single agent, the drug sensitivity testing indicated that higher dose of RRx-001 was required to inhibited 50 % of the parasite's activity (IC50 = 0.14 ± 0.04 ug/ml).IC50 value: 0.14 ± 0.04 ug/ml [1]Target: G6PDin vitro: RRx-001 is a novel, systemically non-toxic, epigenetic anticancer agent for multiple tumour types, with activity mediated through increased nitric oxide (NO) production and PPP inhibition. [1]in vivo: RRx-001is a novel, nonexplosive molecule modified from a class of solid rocket propellants, has shown promise as a novel cancer therapeutic agent in a number of cell lines and tumor models. In mouse models, RRx-001 administered intravenously as a single agent was equipotent to cisplatin while better tolerated. RRx-001 also showed activity as a radiosensitizer in both in vitro and in vivo models. The activity of RRx-001 is thought to be associated with a nucleophilic substitution by circulating thiol compounds and covalent binding of RRx-001 to cysteinyl residues in Hb, followed by the generation of nitrogen oxides. [2]

Name 2-bromo-1-(3,3-dinitroazetidin-1-yl)ethanone
Synonyms RRX-001
UNII-7RPW6SU9SC
1-bromoacetyl-3,3-dinitroazetidine
2-Bromo-1-(3,3-dinitroazetidin-1-yl)ethan-1-one
Description RRx-001 is a potent inhibitor of G6PD. RRx-001 shows potent antimalarial, although as a single agent, the drug sensitivity testing indicated that higher dose of RRx-001 was required to inhibited 50 % of the parasite's activity (IC50 = 0.14 ± 0.04 ug/ml).IC50 value: 0.14 ± 0.04 ug/ml [1]Target: G6PDin vitro: RRx-001 is a novel, systemically non-toxic, epigenetic anticancer agent for multiple tumour types, with activity mediated through increased nitric oxide (NO) production and PPP inhibition. [1]in vivo: RRx-001is a novel, nonexplosive molecule modified from a class of solid rocket propellants, has shown promise as a novel cancer therapeutic agent in a number of cell lines and tumor models. In mouse models, RRx-001 administered intravenously as a single agent was equipotent to cisplatin while better tolerated. RRx-001 also showed activity as a radiosensitizer in both in vitro and in vivo models. The activity of RRx-001 is thought to be associated with a nucleophilic substitution by circulating thiol compounds and covalent binding of RRx-001 to cysteinyl residues in Hb, followed by the generation of nitrogen oxides. [2]
Related Catalog
References

[1]. Yalcin O, et al. From METS to malaria: RRx-001, a multi-faceted anticancer agent with activity in cerebral malaria. Malar J. 2015 May 28;14:218.

[2]. Scicinski J, et al. Preclinical evaluation of the metabolism and disposition of RRx-001, a novel investigative anticancer agent. Drug Metab Dispos. 2012 Sep;40(9):1810-1816.

Molecular Formula C5H6BrN3O5
Molecular Weight 268.02200
Exact Mass 266.94900
PSA 111.95000
LogP 0.45750
Storage condition -20℃
Hazard Codes N

~83%

925206-65-1 structure

925206-65-1

Literature: Straessler, Nichols A.; Lesley, Michael W.; Cannizzo, Louis F. Organic Process Research and Development, 2012 , vol. 16, # 3 p. 512 - 517