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RRx-001(ABDNAZ)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
RRx-001(ABDNAZ)图片
CAS NO:925206-65-1
规格:≥98%
包装与价格:
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

产品介绍
理化性质和储存条件
Molecular Weight (MW)268.02
FormulaC5H6BrN3O5
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 infoChemical 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-]

SynonymsRRX-001; RRX 001; RRx001; ABDNAZ
实验参考方法
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).

In VivoRRx-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 modelCB-17 SCID-mice
Formulation & Dosage5 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.