Top Suppliers:I want be here




877822-41-8

877822-41-8 structure
877822-41-8 structure
  • Name: Eupalinolide A
  • Chemical Name: [(3aR,4R,6Z,9S,10E,11aR)-9-acetyloxy-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate
  • CAS Number: 877822-41-8
  • Molecular Formula: C24H30O9
  • Molecular Weight: 462.490
  • Catalog: Research Areas Cancer
  • Create Date: 2018-08-11 21:26:53
  • Modify Date: 2025-08-25 10:57:51
  • Eupalinolide B is a germacrane sesquiterpene isolated from Eupatorium lindleyanum. Eupalinolide B demonstrates potent cytotoxicity against A-549, BGC-823 and HL-60 tumour cell lines[1].

Name [(3aR,4R,6Z,9S,10E,11aR)-9-acetyloxy-6-(acetyloxymethyl)-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate
Synonyms Eupalinolide A
2-Butenoic acid, 4-hydroxy-2-methyl-, (3aR,4R,6Z,9S,10E,11aR)-9-(acetyloxy)-6-[(acetyloxy)methyl]-2,3,3a,4,5,8,9,11a-octahydro-10-methyl-3-methylene-2-oxocyclodeca[b]furan-4-yl ester, (2E)-
(3aR,4R,6Z,9S,10E,11aR)-9-Acetoxy-6-(acetoxymethyl)-10-methyl-3-methylene-2-oxo-2,3,3a,4,5,8,9,11a-octahydrocyclodeca[b]furan-4-yl (2E)-4-hydroxy-2-methyl-2-butenoate
Description Eupalinolide B is a germacrane sesquiterpene isolated from Eupatorium lindleyanum. Eupalinolide B demonstrates potent cytotoxicity against A-549, BGC-823 and HL-60 tumour cell lines[1].
Related Catalog
References

[1]. Yang NY, et al. Cytotoxic sesquiterpene lactones from Eupatorium lindleyanum. J Asian Nat Prod Res. 2007 Apr-Aug;9(3-5):339-45.

Density 1.24±0.1 g/cm3 (20 ºC 760 Torr)
Boiling Point 618.6±55.0 °C at 760 mmHg
Molecular Formula C24H30O9
Molecular Weight 462.490
Flash Point 205.4±25.0 °C
Exact Mass 462.188995
PSA 125.43000
LogP 2.50
Vapour Pressure 0.0±4.1 mmHg at 25°C
Index of Refraction 1.541
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.