β-Hydroxypropiovanillone, a natural compound, shows significant concentration-dependent inhibitory effects on α-glucosidase with an IC 50 of 257.8 μg/mL In Vitro β-hydroxypropiovanillone and its analogs can be obtained by chemoselective catalytic oxidation of lignin using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone/tert-butyl nitrite/O 2 , followed by cleavage of arylglycerol-β-aryl ether with zinc. In SYK-6 cells, β-hydroxypropiovanillone (HPV) is oxidized to vanilloyl acetic acid (VAA) via vanilloyl acetaldehyde (VAL). The resulting VAA was further converted into vanillate through the activation of VAA by coenzyme A. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:IC50: 257.8 μg/mL (α-glucosidase)
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β-Hydroxypropiovanillone
CAS number：2196-18-1 molecular formula：C10H12O4
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| Chinese alias | β-羟基丙香草酮 | ||
| English alias | Q27283375 | beta-Hydroxypropiovanillone | 4-HYDROXYPROPIOGUAIACONE | CAA19618 | AKOS022645250 | 1-Propanone, 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)- | M22UI268J1 | -Hydroxypropiovanillone; -Hydroxypropioguaiacone | HY-N2929 | 3-hydroxy-1-(4-hydroxy-3-met | ||
| CAS number | 2196-18-1 | molecular formula | C10H12O4 |
| molecular weight | 196.20 g/mol | Exact mass | ≥97% |
| PSA | 66.800 Ų | logp | -0.200 |
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