Name | Corylifol A |
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Synonyms |
4H-1-Benzopyran-4-one, 3-[3-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-4-hydroxyphenyl]-7-hydroxy-
3-{3-[(2E)-3,7-Dimethyl-2,6-octadien-1-yl]-4-hydroxyphenyl}-7-hydroxy-4H-chromen-4-one |
Description | Corylifol A inhibits IL-6-induced STAT3 activation and phosphorylation, with an IC50 of 0.81 μM. |
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Related Catalog | |
Target |
STAT3:0.81 μM (IC50) |
In Vitro | Corylifol A shows an inhibitory effect on IL-6-induced STAT3 promoter activity in Hep3B cells with IC50 value of 0.81±0.15 μM, also inhibits STAT3 phosphorylation induced by IL-6 in Hep3B cells[1]. Corylifol A inhibits SARA PLpro in a dose-dependent manner with IC50s ranging between 4.2 and 38.4 μM[2]. Corylifol A is found to be a naturally occurring potent inhibitor of hCE2, with low Ki values ranging from 0.62 μM to 3.89 μM[3]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 609.3±55.0 °C at 760 mmHg |
Molecular Formula | C25H26O4 |
Molecular Weight | 390.471 |
Flash Point | 208.8±25.0 °C |
Exact Mass | 390.183105 |
PSA | 70.67000 |
LogP | 6.91 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.615 |
Storage condition | -20°C |