Weight | 166.176 g/mol |
---|---|
Formula | C9H10O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Acetovanillone (498-02-2)
apocynin · 4-hydroxy-3-methoxyacetophenone · apocynine
Score:
#891 in Neuroscience
,
#1795 in Biochemistry
,
#3922 in Biology
,
#4934 in Chemistry
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- Apocynin Is Not an Inhibitor of Vascular NADPH Oxidases but an Antioxidant (Hypertension, 2008)
- Characteristics of the inhibition of NADPH oxidase activation in neutrophils by apocynin, a methoxy-substituted catechol. (American Journal of Respiratory Cell and Molecular Biology, 1994)
- Apocynin protects against global cerebral ischemia-reperfusion-induced oxidative stress and injury in the gerbil hippocampus (Brain Research, 2006)
- Apocynin: Molecular Aptitudes (Mediators of Inflammation, 2008)
- Effects of methoxylation of apocynin and analogs on the inhibition of reactive oxygen species production by stimulated human neutrophils (European Journal of Pharmacology, 2001)
- Apocynin inhibits NADPH oxidase in phagocytes but stimulates ROS production in non-phagocytic cells (Biochimica et Biophysica Acta, 2005)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - apocynin
- 4-hydroxy-3-methoxyacetophenone
- apocynine
- 4'-hydroxy-3'-methoxyacetophenone
-
SMILESCC(=O)C1=CC(=C(C=C1)O)OC
-
InChIKeyDFYRUELUNQRZTB-UHFFFAOYSA-N
- Pubchem - Acetovanillone
- Wikipedia - apocynin
Apocynin, also known as acetovanillone, is a natural organic compound structurally related to vanillin. It has been isolated from a variety of plant sources and is being studied for its variety of pharmacological properties.
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methyl 4-(3,4-dimethoxyphenyl)-4-oxobutanoate
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99-40-1
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