Name | Chevalone C |
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Synonyms |
1H,11H-Phenanthro[2,1-b]pyrano[3,2-e]pyran-11-one, 2-(acetyloxy)-2,3,4,4a,4b,5,6,6a,12,12a,12b,13,14,14a-tetradecahydro-1,1,4a,6a,9,12b-hexamethyl-, (2S,4aR,4bR,6aS,12aS,12bR,14aR)-
(2S,4aR,4bR,6aS,12aS,12bR,14aR)-1,1,4a,6a,9,12b-Hexamethyl-11-oxo-2,3,4,4a,4b,5,6,6a,12,12a,12b,13,14,14a-tetradecahydro-1H,11H-naphtho[2,1-f]pyrano[2,3-b]chromen-2-yl acetate Chevalone C |
Description | Chevalone C, a meroterpenoid fungal metabolite, shows antimalarial activity with IC50 value of 25.00 μg/mL. Chevalone C has anti-proliferative activity on colon HCT116, liver HepG2 and melanoma A375 cancer cell lines[1][2]. |
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Related Catalog | |
In Vitro | Chevalone C (1, 10, 50, 100, 200 μM; 24 hours) exhibits a significant decrease of cell viability in HepG2, HCT116 and HT29 cell lines (ic50=153 μM, 190 μM, 98 μM)[2]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 541.2±50.0 °C at 760 mmHg |
Molecular Formula | C28H40O5 |
Molecular Weight | 456.614 |
Flash Point | 256.5±18.1 °C |
Exact Mass | 456.287567 |
LogP | 6.52 |
Vapour Pressure | 0.0±1.4 mmHg at 25°C |
Index of Refraction | 1.551 |