3-Hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione

Product Description

3-Hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione
Catalog number: B2010475
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 10 mg
Molecular Weight or Concentration: 179.17
Supplied as: Powder
Appearance: Powder
Applications: This quality compound has several applications in chemistry, biochemistry, cellular biology and other domains. Bulk orders of this product are available upon request.
Storage: -20C
Keywords: 3-Hydroxy-1-methyl-5,6-indolinedione
Grade: Biotechnology grade. All solid components are highly pure (minimum 95%). All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
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2: Toulouse C, Schmucker S, Metesch K, Pfannstiel J, Michel B, Starke I, Möller HM, Stefanski V, Steuber J. Mechanism and impact of catecholamine conversion by Vibrio cholerae Biochim Biophys Acta Bioenerg. 2019 Jun 1;1860(6):478-487.
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5: Chen C, Thakker DR. The fallacy of using adrenochrome reaction for measurement of reactive oxygen species formed during cytochrome p450-mediated metabolism of xenobiotics J Pharmacol Exp Ther. 2002 Feb;300(2):417-20.
6: Alejandria M. Dengue fever Clin Evid. 2005 Jun;(13):887-95.
7: GAUTHERON D, CHAIX P. [The oxidation of adrenochrome] Biochim Biophys Acta. 1954 Feb;13(2):299-300.
8: Mills JA. Hallucinogens as hard science: the adrenochrome hypothesis for the biogenesis of schizophrenia Hist Psychol. 2010 May;13(2):178-95.
9: Miller CL. The chemical interaction between adrenochrome, three different classes of antipsychotic drugs and metabolites of the kynurenine pathway Eur Neuropsychopharmacol. 2015 Mar;25(3):435-40.
10: Foster HD, Hoffer A. Schizophrenia and cancer: the adrenochrome balanced morphism Med Hypotheses. 2004;62(3):415-9.

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