Basic information Safety Supplier Related

DMNQ

Basic information Safety Supplier Related

DMNQ Basic information

Product Name:
DMNQ
Synonyms:
  • DMNQ
  • DIMENQ
  • 2,3-DIMETHOXY-1,4-NAPHTHOQUINONE
  • RARECHEM BW GA 0209
  • 1,4-Naphthalenedione, 2,3-dimethoxy-
  • Nsc 69355
  • 2,3-dimethoxynaphthalene-1,4-dione
  • 2,3-Dimethoxy-1,4-naphthalenedione
CAS:
6956-96-3
MF:
C12H10O4
MW:
218.21
EINECS:
604-604-1
Mol File:
6956-96-3.mol
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DMNQ Chemical Properties

storage temp. 
-20°C
solubility 
Soluble in DMSO (up to 10 mg/ml) or in Ethanol (up to 5 mg/ml).
form 
solid
color 
Yellow
Stability:
Stable for 1 year as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3

MSDS

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DMNQ Usage And Synthesis

Description

DMNQ is a 1,4-naphthoquinone that acts as a redox-cycling agent, typically increasing intracellular superoxide and hydrogen peroxide formation. The amount of oxidative stress is proportional to the amount of DMNQ applied and can alter diverse cellular parameters, including signal transduction, mitochondrial function, and gene expression.

Uses

DMNQ is a non-alkylating redox cycling quinone.

Uses

2,3-Dimethoxy-1,4-naphthoquinone has been used to investigate the effects of ethanol on podocyte apoptosis under hypoxic and hyperoxic conditions.

Definition

ChEBI: A naphthoquinone that is 1,4-naphthoquinone bearing two methoxy substituents at positions 2 and 3. Redox-cycling agent that induces intracellular superoxide anion formation and, depending on the concentration, induces cell proliferation, apoptosis or necro is. Used to study the role of ROS in cell toxicity, apoptosis, and necrosis.

Biochem/physiol Actions

2,3-dimethoxy-1,4-naphthoquinone (DMNQ) has the ability to produce H2O2?through redox cycling but fails to conjugate with glutathione (GSH).

storage

+4°C

References

References/Citations 1) Gant?et al. (1988)?Redox Cycling and Sulphydryl Arylation; Their Relative Importance in the Mechanism of Quinone Cytotoxicity to Isolated Hepatocytes; Chem. Biol. Interactions;?65?157 2) Stubberfield and Cohen (1989)?Interconversion of NAD(H) to NADP(H). A cellular response to quinone-induced oxidative stress in isolated hepatocytes; Biochem. Pharmacol.,?38?2631 3) Dypbukt?et al?(1994)?Different prooxidant levels stimulate growth, trigger apoptosis or produce necreosis of insulin-secreting RINm5F cells. The role of intracellular polyamines; J. Biol. Chem.,?269?30553 4) Henry and Wallace (1996)?Differential mechanisms of cell killing by redox cycling and arylating quinones; Arch. Toxicol.,?70?482

DMNQSupplier

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