Name | (3S,5S,9R,10S,13R,14R,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol |
---|---|
Synonyms |
a-Spinasterin
Bessisterol UNII:0LG993QX1A Spinasterol (3b,5a,22E)-Stigmasta-7,22-dien-3-ol Alpha-Spinasterol spinasta-7,22-dien-3-ol Hitodesterol Chondrillasterol a-Spinasterol Stigmasta-7,22-dien-3-ol, (3β,5α,22E)- α-Spinasterin (3β,5α,22E)-Stigmasta-7,22-dien-3-ol |
Description | α-Spinasterol, isolated from Spinacia oleracea, has antibacterial activity[1]. α-Spinasterol is a transient receptor potential vanilloid 1 (TRPV1) antagonist, has anti-inflammatory, antidepressant, antioxidant and antinociceptive effects. α-Spinasterol inhibits COX-1 andCOX-2 activities with IC50 values of 16.17 μM and 7.76 μM, respectively[2]. |
---|---|
Related Catalog | |
Target |
COX-1:16.17 μM (IC50) COX-2:7.76 μM (IC50) TRPV1 |
References |
Density | 1.0±0.1 g/cm3 |
---|---|
Boiling Point | 500.0±44.0 °C at 760 mmHg |
Melting Point | 168-169° |
Molecular Formula | C29H48O |
Molecular Weight | 412.691 |
Flash Point | 219.1±20.7 °C |
Exact Mass | 412.370514 |
PSA | 20.23000 |
LogP | 10.13 |
Vapour Pressure | 0.0±2.9 mmHg at 25°C |
Index of Refraction | 1.531 |
Storage condition | 2-8℃ |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
Hazard Codes | Xi |
---|