Name | sugiol |
---|---|
Synonyms |
9(1H)-Phenanthrenone, 2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS,10aS)-
12-Hydroxyabieta-8,11,13-triene-7-one 7-oxo-8,11,13-abietatrien-12-ol 12-Hydroxy-abieta-8,11,13-trien-7-on 9(1H)-Phenanthrenone, 2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS-trans)- Podocarpa-8,11,13-trien-7-one, 12-hydroxy-13-isopropyl- 12-hydroxy-abieta-8,11,13-trien-7-one 12-Hydroxyabieta-8(14),9(11),12-trien-7-one 10-Deoxoxanthoperol 12-hidroxyabieta-8,11,13-trien-7-one |
Description | Sugiol is an abietane diterpenoid, can be isolated from Calocedrus formosana bark. Sugiol has anti-inflammatory activity, could effectively reduce intracellular reactive oxygen species (ROS) production in lipopolysaccharide (LPS)-stimulated macrophages[1]. |
---|---|
Related Catalog | |
Target |
ERK1 ERK2 p38 MAPK JNK1 JNK2 IL-1β |
In Vitro | Sugiol (5-30 μM; 30 min) 抑制 J774A 细胞中 TNF-α 和 proIL-1β/IL-1β 蛋白的产生[1]。 Sugiol (5-30 μM; 30 min) 在脂多糖诱导的 J774A 细胞中抑制 MAPK 激活,抑制 ERK1/2, JUNK1/2 和 p38 磷酸化[1]。 Western Blot Analysis[1] Cell Line: J774A.1 macrophages cells stimulated with LPS Concentration: 5 μM, 10 μM, 20 μM, and 30 μM Incubation Time: 30 min Result: Completely inhibited ERK1/2 phosphorylation at 30 μM, and effectively inhibited JNK1/2 and p38 phosphorylation. |
References |
Density | 1.0±0.1 g/cm3 |
---|---|
Boiling Point | 437.2±45.0 °C at 760 mmHg |
Molecular Formula | C20H28O2 |
Molecular Weight | 300.435 |
Flash Point | 186.4±21.3 °C |
Exact Mass | 300.208923 |
PSA | 37.30000 |
LogP | 6.77 |
Vapour Pressure | 0.0±1.1 mmHg at 25°C |
Index of Refraction | 1.539 |
Hazard Codes | Xi |
---|