[CAS NO. 925206-65-1]  RRx-001

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PRODUCTS SPECIFICATIONS [925206-65-1]

Store
Catalog
SLK-S8405
Brand
Selleck
CAS
925206-65-1

DESCRIPTION [925206-65-1]

Overview

MDLMFCD25976849
Molecular Weight268.02
Molecular FormulaC5H6BrN3O5
SMILESO=C(N1CC([N+]([O-])=O)([N+]([O-])=O)C1)CBr

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM3.7311 mL18.6553 mL37.3106 mL
5 mM0.7462 mL3.7311 mL7.4621 mL
10 mM0.3731 mL1.8655 mL3.7311 mL
50 mM0.0746 mL0.3731 mL0.7462 mL

Description

RRx-001 is a novel modulator with potential radiosensitizing activity. It inhibits in human tumor cells, binds hemoglobin and drives RBC-mediated redox reactions under hypoxia. RRx-001 triggers and exhibits anticancer activity.

Targets

G6PD [1]Nrf2-ARE [3]

In vitro

RRx-001 exerts its anti-proliferative effect, at least partially, through interference with glucose 6 phosphate dehydrogenase (G6PD), a key enzyme in the pentose phosphate pathway, responsible for maintaining adequate levels of the major cellular reductant, NADPH. RRx-001 affects glucose and G6PD enzyme activity in three different cancer cell lines namely Hep G2, CACO-2, and HT-29. RRx-001 induced G6PD inhibition and increased glucose consumption in a concentration dependent fashion. RRx-001 induces p53 and PARP-1 via generation of ROS/RNS. It exerts anticancer activity, at least in part, by interfering with 3 crucial metabolic demands of rapidly proliferating cells: bioenergetics, macromolecular biosynthesis, and manipulation of cellular cytosolic redox homeostasis. RRx-001 mediates nuclear translocation of Nrf2 and the activation of expression of its downstream enzymes HO-1 and NQO1 in tumor cells. Apart from epigenetic alterations, RRx-001 acts via pleiotropic mechanisms including redox signaling and redox-induced dysregulation of many different signal pathways such as Nrf2, p53, PARP cleavage, HIF1 alpha, and G6PD activity. It also triggers p53 and p21 activity in response to double-stranded DNA breaks as well as deregulates cancer cellular energetics and metabolism. RRx-001 is a potent activator of the Nrf2-ARE signaling pathway via ROS/RNS generation.

In vivo

RRx-001 shows promise for short-term blood flow redistribution in tumors with a pericyte- and α-SMA-rich vasculature. RRx-001 monotherapy is well tolerated, with no dose-limiting toxicities. It not only facilitates nuclear translocation of Nrf2, but also upregulates endogenous Nrf2 expression in SCC VII tumors in mice.