Name | Psoralenoside |
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Synonyms |
(2Z)-3-[6-(β-D-Glucopyranosyloxy)-1-benzofuran-5-yl]acrylic acid
2-Propenoic acid, 3-[6-(β-D-glucopyranosyloxy)-5-benzofuranyl]-, (2Z)- |
Description | Psoralenoside is a benzofuran glycoside from Psoralea corylifolia[1]. Psoralenoside exhibits high binding affinities against histaminergic H1, calmodulin, and voltage-gated L-type calcium channels (E-value≥-6.5 Kcal/mol)[2]. Psoralenoside shows estrogen-like activity, osteoblastic proliferation accelerating activity, antitumor effects and antibacterial activity[3]. |
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Related Catalog | |
Target |
H1 Receptor L-type calcium channel |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 662.4±55.0 °C at 760 mmHg |
Molecular Formula | C17H18O9 |
Molecular Weight | 366.319 |
Flash Point | 354.4±31.5 °C |
Exact Mass | 366.095093 |
LogP | -0.02 |
Vapour Pressure | 0.0±2.1 mmHg at 25°C |
Index of Refraction | 1.711 |