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AB144626

DMNQ, non-alkyiating redox cycling quinone

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MW 218.2 Da, Purity >99%. Cell-permeable, non-alkylating redox cycling quinone. Generates superoxide production and induces cell proliferation, apoptosis and necrosis in vitro. Redox cycling agent. Active in vivo and in vitro.
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Chemical Structure - DMNQ, non-alkyiating redox cycling quinone (AB144626)
  • Chemical Structure

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Chemical Structure - DMNQ, non-alkyiating redox cycling quinone (AB144626)

2D chemical structure image of ab144626, DMNQ, non-alkyiating redox cycling quinone

Key facts

CAS number

6956-96-3

Purity

>99%

Form

Solid

form

Molecular weight

218.2 Da

Molecular formula

C<sub>1</sub><sub>2</sub>H<sub>1</sub><sub>0</sub>O<sub>4</sub>

PubChem

3136

Nature

Synthetic

Solubility

Soluble in DMSO to 25 mM

Biochemical name

2,3-Dimethoxy-1,4-naphthoquinone

Biological description

Cell-permeable, non-alkylating redox cycling quinone. Generates superoxide production and induces cell proliferation, apoptosis and necrosis in vitro. Redox cycling agent. Active in vivo and in vitro.

Canonical smiles

COC1=C(C(=O)C2=CC=CC=C2C1=O)OC

InChi

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

IUPAC Name

2,3-dimethoxynaphthalene-1,4-dione

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months

Product protocols

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