CAS NO: | 925206-65-1 |
规格: | ≥98% |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
250mg | 电议 |
500mg | 电议 |
Molecular Weight (MW) | 268.02 |
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Formula | C5H6BrN3O5 |
CAS No. | 925206-65-1 |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility (In vitro) | DMSO: 53 mg/mL (197.7 mM) |
Water: <1 mg/mL | |
Ethanol: 23 mg/mL (85.8 mM) | |
Other info | Chemical Name: 2-bromo-1-(3,3-dinitroazetidin-1-yl)ethanone InChi Key: JODKFOVZURLVTG-UHFFFAOYSA-N InChi Code: InChI=1S/C5H6BrN3O5/c6-1-4(10)7-2-5(3-7,8(11)12)9(13)14/h1-3H2 SMILES Code: O=[N+](C1([N+]([O-])=O)CN(C(CBr)=O)C1)[O-] |
Synonyms | RRX-001; RRX 001; RRx001; ABDNAZ |
In Vitro | In vitro activity: 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. Kinase Assay: 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). |
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In Vivo | RRx-001 is 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. |
Animal model | CB-17 SCID-mice |
Formulation & Dosage | 5 mg/kg or 10 mg/kg; i.v. |
References | Malar J. 2015 May 28;14:218; Drug Metab Dispos. 2012 Sep;40(9):1810-6; Leukemia. 2016 Nov;30(11):2187-2197. |