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Key Documents

SML3192

Sigma-Aldrich

GLX481304

≥98% (HPLC)

Synonym(s):

2-N-(3,4-Dimethylphenyl)-6-[[4-(3-methoxyphenyl)piperazin-1-yl]methyl]-1,3,5-triazine-2,4-diamine, N-(3,4-Dimethylphenyl)-6-[[4-(3-methoxyphenyl)-1-piperazinyl]methyl]-1,3,5-triazine-2,4-diamine, N2-(3,4-Dimethylphenyl)-6-[[4-(3-methoxyphenyl)-1-piperazinyl]methyl]-1,3,5-triazine-2,4-diamine, [4-Amino-6-[4-(3-methoxy-phenyl)-piperazin-1-ylmethyl]-1H-[1,3,5]triazin-2-ylidene]-(3,4-dimethyl-phenyl)-amine

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About This Item

Empirical Formula (Hill Notation):
C23H29N7O
CAS Number:
Molecular Weight:
419.52
UNSPSC Code:
12352107

Quality Level

Assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Biochem/physiol Actions

GLX481304 is a cell-permeable, noncytotoxic triazine-diamino compound that acts a potent, dual NOX2 and NOX4 isoform-selective inhibitor (IC50 ~ 1.25 μM) over NOX1. Does neither function as an antioxidant nor as a scavenger of reactive oxygen species (ROS). GLX481304 is shown to dose-dependently reduce ROS levels in hypoxia challenged mouse cardiomyocytes and improve contractile function in whole heart.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Ferenc L M Szekeres et al.
Scientific reports, 11(1), 11970-11970 (2021-06-09)
The NADPH oxidase enzymes Nox2 and 4, are important generators of Reactive oxygen species (ROS). These enzymes are abundantly expressed in cardiomyocytes and have been implicated in ischemia-reperfusion injury. Previous attempts with full inhibition of their activity using genetically modified
Isabel Cordero-Herrera et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(1), 217-226 (2018-12-19)
Advanced age and unhealthy dietary habits contribute to the increasing incidence of obesity and type 2 diabetes. These metabolic disorders, which are often accompanied by oxidative stress and compromised nitric oxide (NO) signaling, increase the risk of adverse cardiovascular complications

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