Name | (1S,2S,3R,5R,6S,7R,14R,15S,18R,21S,22R,25S)-5,7,18-Trihydroxy-1,14,21,25-tetramethyl-4,20,23-trioxaheptacyclo[20.3.1.12,5.03,18.03,21.06,15.09,14]heptacosa-8,10-diene-13,19,24,27-tetrone |
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Synonyms |
1,17:2,6-Dimethano-8H-naphtho[1,2-f]furo[3,4-b:2,3-c']bisoxocin-4,8,11,19(1H,10H)-tetrone, 2,3,6,6a,8a,9,10a,10b,12,16,16a,17-dodecahydro-8a,16,17-trihydroxy-2,3,6a,10b-tetramethyl-, (1R,2S,3S,6R,6aS,8aS,10aS,10bR,16R,16aS,17R,18aR)-
(1S,2R,3R,5R,6S,7R,14R,15S,18S,21S,22R,25S)-5,7,18-Trihydroxy-1,14,21,25-tetramethyl-4,20,23-trioxaheptacyclo[20.3.1.1.0.0.0.0]heptacosa-8,10-diene-13,19,24,27-tetrone |
Description | Physalin L inhibits LPS-induced NO production in macrophages with the average inhibitory rate of 70.97%. Anti-inflammatory activity[1]. |
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Related Catalog | |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 831.1±65.0 °C at 760 mmHg |
Molecular Formula | C28H32O10 |
Molecular Weight | 528.548 |
Flash Point | 280.4±27.8 °C |
Exact Mass | 528.199524 |
PSA | 156.66000 |
LogP | 2.07 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.659 |