2,3-Dimethoxy-5-methyl-1,4-benzoquinone (Highly Pure)

• Description:

  2,3-Dimethoxy-5-methyl-1,4-benzoquinone (Highly Pure)_x000D_ Catalog number: B2012388_x000D_ Lot number: Batch Dependent_x000D_ Expiration Date: Batch dependent_x000D_ Amount: 25 mg_x000D_ Molecular Weight or Concentration: 182.18_x000D_ Supplied as: Powder_x000D_ Applications: molecular tool for various biochemical applications_x000D_ Storage: RT_x000D_ Keywords: Coenzyme Q10_x000D_ Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ References:_x000D_ 1: Roginsky VA, Bruchelt G, Bartuli O. Ubiquinone-0 (2,3-dimethoxy-5-methyl-1,4-benzoquinone) as effective catalyzer of ascorbate and epinephrine oxidation and damager of neuroblastoma cells Biochem Pharmacol. 1998 Jan 1;55(1):85-91._x000D_ 2: Amano T, Terao S, Imada I. Effects of 6-(10-hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (idebenone) and related benzoquinones on porcine pancreas phospholipase A2 activity Biol Pharm Bull. 1995 May;18(5):779-81._x000D_ 3: Belliere J, Devun F, Cottet-Rousselle C, Batandier C, Leverve X, Fontaine E. Prerequisites for ubiquinone analogs to prevent mitochondrial permeability transition-induced cell death J Bioenerg Biomembr. 2012 Feb;44(1):207-12._x000D_ 4: Hseu YC, Tseng YF, Pandey S, Shrestha S, Lin KY, Lin CW, Lee CC, Huang ST, Yang HL. Coenzyme Q(0) Inhibits NLRP3 Inflammasome Activation through Mitophagy Induction in LPS/ATP-Stimulated Macrophages Oxid Med Cell Longev. 2022 Jan 7;2022:4266214._x000D_ 5: Sanchez-Cruz P, Garcia C, Alegria AE. Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione Free Radic Biol Med. 2010 Nov 15;49(9):1387-94._x000D_ 6: Sugihara H, Watanabe M, Kawamatsu Y, Morimoto H. [Ubiquinones and related compounds. XXII. Synthesis of 2,3-dimethoxy-5-methyl-1,4-benzoquinone and its ethylhomologues] Justus Liebigs Ann Chem. 1972 Sep;763:109-20._x000D_ 7: Okamoto K, Watanabe M, Morimoto H, Imada I. Synthesis, metabolism, and in vitro biological activities of 6-(10-hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (CV-2619)-related compounds Chem Pharm Bull (Tokyo). 1988 Jan;36(1):178-89._x000D_ 8: Okamoto K, Imada I, Imamoto T. Effect of 6-(10-hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (CV-2619) on microsomal lipid peroxidation Chem Pharm Bull (Tokyo). 1986 Jul;34(7):2821-7._x000D_ 9: Sanchez-Cruz P, Santos A, Diaz S, Alegría AE. Metal-independent reduction of hydrogen peroxide by semiquinones Chem Res Toxicol. 2014 Aug 18;27(8):1380-6._x000D_ 10: Kobayashi T, Yoshida K, Mitani M, Torii H, Tanayama S. Metabolism of idebenone (CV-2619), a new cerebral metabolism improving agent: isolation and identification of metabolites in the rat and dog J Pharmacobiodyn. 1985 Jun;8(6):448-56. _x000D_ _x000D_ Products Related to 2,3-Dimethoxy-5-methyl-1,4-benzoquinone (Highly Pure) can be found at Chemicals

• Short Description:

  Catalog Number: B2012388 (25 mg)

• Weight:

  0.15

• Length:

  2

• Width:

  0.5

• Height:

  0.5

• Height :

  0.5