[3-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate

Modify Date: 2024-01-13 18:30:54

[3-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate Structure
[3-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate structure
Common Name [3-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate
CAS Number 4029-69-0 Molecular Weight 486.59700
Density 1.24g/cm3 Boiling Point 596.6ºC at 760 mmHg
Molecular Formula C28H38O7 Melting Point N/A
MSDS N/A Flash Point 191.9ºC

 Use of [3-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate


3-O-Acetylbufotalin is a derivate of bufadienolide, with anti-cancer activity[1].

 Names

Name Bufotalin 3-acetate
Synonym More Synonyms

  Biological Activity

Description 3-O-Acetylbufotalin is a derivate of bufadienolide, with anti-cancer activity[1].
Related Catalog
In Vitro 3-O-Acetylbufotalin (2b) inhibits the growth of six human cancer cell lines, with a mean IC50 of 159 nM[1].
References

[1]. Moreno Y Banuls L, et al. Structure-activity relationship analysis of bufadienolide-induced in vitro growth inhibitory effects on mouse and human cancer cells.

 Chemical & Physical Properties

Density 1.24g/cm3
Boiling Point 596.6ºC at 760 mmHg
Molecular Formula C28H38O7
Molecular Weight 486.59700
Flash Point 191.9ºC
Exact Mass 486.26200
PSA 103.04000
LogP 4.35430
Vapour Pressure 1.02E-16mmHg at 25°C
Index of Refraction 1.57

 Synonyms

digitoxigenin3-rhamnoside
evomonosid
a-hydroxy
3-O-acetylbufotalin
digitoxigenin rhamnoside
DIGITOXIGENIN-3-O-A-L-RHAMNOPYRANOSIDE
DIGITOXIGENIN-3-O-RHAMNOSIDE
Digitoxigenine-3-rhamnoside