Name | 13-[3,5-Dihydroxy-4-(3-phenylpropanoyl)phenoxy]-2,3,4,5,6,7,14-heptahydroxy-15-[2-oxo-2-(3,4,5-trihydroxyphenyl)ethyl]-11,11a,13,14,15,15a-hexahydrodibenzo[g,i]pyrano[3,2-b][1,5]dioxacycloundecine-9,17-dione |
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Synonyms |
13-[3,5-Dihydroxy-4-(3-phenylpropanoyl)phenoxy]-2,3,4,5,6,7,14-heptahydroxy-15-[2-oxo-2-(3,4,5-trihydroxyphenyl)ethyl]-11,11a,13,14,15,15a-hexahydrodibenzo[g,i]pyrano[3,2-b][1,5]dioxacycloundecine-9,17-dione
Dibenzo[g,i]pyrano[3,2-b][1,5]dioxacycloundecin-9,17-dione, 13-[3,5-dihydroxy-4-(1-oxo-3-phenylpropyl)phenoxy]-11,11a,13,14,15,15a-hexahydro-2,3,4,5,6,7,14-heptahydroxy-15-[2-oxo-2-(3,4,5-trihydroxyphenyl)ethyl]- Thonningianin A |
Description | Thonningianin A, an ellagitannin, is isolated from the methanolic extract of the African medicinal herb, Thonningia sanguinea. The antioxidant properties of Th A involve radical scavenging, anti-superoxide formation and metal chelation. Anti-cancer activities[1][2]. |
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Related Catalog | |
In Vitro | Thonningianin A effectively inhibited the proliferation of HepG-2 cells by inducing apoptosis, as evidenced by increase in the sub-G1 cell population, DNA fragmentation, and increase in the content of reactive oxygen species[2]. |
References |
Density | 1.7±0.1 g/cm3 |
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Boiling Point | 1365.2±65.0 °C at 760 mmHg |
Molecular Formula | C42H34O21 |
Molecular Weight | 872.734 |
Flash Point | 412.3±27.8 °C |
Exact Mass | 872.179993 |
LogP | 6.13 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.733 |
Storage condition | -20℃ |