| Identification | Back Directory | [Name]
DMNQ | [CAS]
6956-96-3 | [Synonyms]
DMNQ
DIMENQ
Nsc 69355
RARECHEM BW GA 0209
2,3-DIMETHOXY-1,4-NAPHTHOQUINONE
2,3-dimethoxynaphthalene-1,4-dione
2,3-Dimethoxy-1,4-naphthalenedione
1,4-Naphthalenedione, 2,3-dimethoxy- | [EINECS(EC#)]
604-604-1 | [Molecular Formula]
C12H10O4 | [MDL Number]
MFCD00184331 | [MOL File]
6956-96-3.mol | [Molecular Weight]
218.21 |
| Chemical Properties | Back Directory | [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. | [InChI]
1S/C12H10O4/c1-15-11-9(13)7-5-3-4-6-8(7)10(14)12(11)16-2/h3-6H,1-2H3 | [InChIKey]
ZEGDFCCYTFPECB-UHFFFAOYSA-N | [SMILES]
COC1=C(OC)C(=O)c2ccccc2C1=O |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38 | [Safety Statements ]
26-36 | [WGK Germany ]
3
| [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [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]
2,3-Dimethoxy-1,4-naphthoquinone has been used to investigate the effects of ethanol on podocyte apoptosis under hypoxic and hyperoxic conditions. | [Uses]
DMNQ is a non-alkylating redox cycling quinone. | [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 |
|
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J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Sigma-Aldrich
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021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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cjbscvictory
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13348960310 13348960310 |
| Website: |
www.weikeqi-biotech.com/ |
| Company Name: |
Bide Pharmatech Ltd.
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| Telephone: |
400-1647117 13681763483 |
| Website: |
https://www.bidepharm.com/ |
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