Name | shionone |
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Synonyms |
(1R,4aS,4bS,6aS,8R,10aR,10bS,12aS)-1,4b,6a,8,10a,12a-Hexamethyl-8-(4-methylpent-3-en-1-yl)hexadecahydrochrysen-2(1H)-one
SHIONONE 21-Shionen-3-one (1R,4aS,4bS,6aS,8R,10aR,10bS,12aS)-1,4b,6a,8,10a,12a-Hexamethyl-8-(4-methyl-3-penten-1-yl)hexadecahydro-2(1H)-chrysenone 2(1H)-Chrysenone, hexadecahydro-1,4b,6a,8,10a,12a-hexamethyl-8-(4-methyl-3-penten-1-yl)-, (1R,4aS,4bS,6aS,8R,10aR,10bS,12aS)- 3b,5a,8,17ab-Tetramethyl-3-(4-methyl-3-pentenyl)-D-homoandrostan-17-one 18,19-Seco-D:A-friedolup-19-en-3-one D:A-Friedo-18,19-secolup-19-en-3-one |
Description | Shionone is the major triterpenoid isolated from Aster tataricus, has anti-tussive, anti-inflammatory activities[1][2]. Shionone possesses a unique six-membered tetracyclic skeleton and 3-oxo-4-monomethyl structure[1]. |
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Related Catalog | |
In Vivo | Shionone (orally administration; 80 mg/kg; 3 days; once daily) shows the trend of enhancing sputum secreting, but has no effect on ammonia-induced cough and reduces xylene-induced ear edema[1]. Animal Model: ICR male mice[1] Dosage: 80 mg/kg Administration: Orally administration; 3 days; once daily Result: Reduced the ear edema for 11.3% by use shionone. |
References |
Density | 0.9±0.1 g/cm3 |
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Boiling Point | 485.6±14.0 °C at 760 mmHg |
Melting Point | 161-162° |
Molecular Formula | C30H50O |
Molecular Weight | 426.717 |
Flash Point | 200.5±15.1 °C |
Exact Mass | 426.386169 |
PSA | 17.07000 |
LogP | 11.00 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.498 |
Safety Phrases | 24/25 |
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HS Code | 29143990 |