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Coronalolide

Names

[ CAS No. ]:
268214-51-3

[ Name ]:
Coronalolide

[Synonym ]:
3-[(1aS,3aR,4R,6aS,6bS,7aR,10aR,10bR)-3a,6a-Dimethyl-10-methylene-4-[(2R,5E)-6-methyl-7-oxo-5-hepten-2-yl]-9-oxododecahydro-1H-cyclopenta[7,8]cyclopropa[4,4a]naphtho[2,3-b]furan-10b(2H)-yl]propanoic acid
1H-Cyclopenta[7,8]cyclopropa[4,4a]naphtho[2,3-b]furan-10b(2H)-propanoic acid, 4-[(1R,4E)-1,5-dimethyl-6-oxo-4-hexen-1-yl]dodecahydro-3a,6a-dimethyl-10-methylene-9-oxo-, (1aS,3aR,4R,6aS,6bS,7aR,10aR,10bR)-
1H-Cyclopenta[7,8]cyclopropa[4,4a]naphtho[2,3-b]furan-10b(2H)-propanoic acid, 4-[(1R,4E)-1,5-dimethyl-6-oxo-4-hexenyl]dodecahydro-3a,6a-dimethyl-10-methylene-9-oxo-, (1aS,3aR,4R,6aS,6bS,7aR,10aR,10bR)

Biological Activity

[Description]:

Coronalolide is a natural triterpene with anticancer effects. Coronalolide exhibits a broad cytotoxic activity for human breast (BT474), gastric (KATO-3), lung (CHAGO), colon (SW-620), and liver (Hep-G2) cancer cell lines, with IC50 values of 6.59 µg/mL, 5.85 µg/mL, 5.42 µg/mL, 4.98 µg/mL, and 6.41 µg/mL, respectively[1].

[Related Catalog]:

Research Areas >> Cancer
Signaling Pathways >> Others >> Others

[References]

[1]. Thanesuan Nuanyai, et al. Cytotoxic 3,4-seco-cycloartane triterpenes from Gardenia sootepensis. J Nat Prod. 2009 Jun;72(6):1161-4.  

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
646.3±20.0 °C at 760 mmHg

[ Molecular Formula ]:
C30H42O5

[ Molecular Weight ]:
482.651

[ Flash Point ]:
208.2±15.3 °C

[ Exact Mass ]:
482.303223

[ PSA ]:
80.67000

[ LogP ]:
5.95

[ Vapour Pressure ]:
0.0±4.2 mmHg at 25°C

[ Index of Refraction ]:
1.562

Safety Information

[ Hazard Codes ]:
Xi

Related Compounds