Name | 2-Butenoic acid, 4-hydroxy-2-(hydroxymethyl)-, 9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl ester, [3aR-[3aR*,4R*(Z),6E,9S*,10Z,11aR*]] |
---|---|
Synonyms |
germacranolide eucannabinolide
Hiyodorilactone A Eucannabinolide Eucannabinolid Schkuhrin I (E)-4-Hydroxy-2-hydroxymethyl-2-butenoic acid (3aR,4R,6E,9S,10Z,11aR)-9-acetoxy-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl ester Hyodorilactone A |
Description | Eucannabinolide is a STAT3 inhibitor. Eucannabinolide suppresses STAT3 activation at tyrosine 705, inhibiteds its translocation to nucleus, and decreases its DNA binding capacity. Eucannabinolide can be used for triple negative breast cancer (TNBC) diseases research[1]. |
---|---|
Related Catalog | |
References |
Density | 1.26g/cm3 |
---|---|
Boiling Point | 618.9ºC at 760 mmHg |
Molecular Formula | C22H28O8 |
Molecular Weight | 420.45 |
Flash Point | 211.5ºC |
Exact Mass | 420.17800 |
PSA | 119.36000 |
LogP | 1.52510 |
Index of Refraction | 1.555 |
Hazard Codes | Xi |
---|
Precursor 9 | |
---|---|
DownStream 0 |