
Chrysin 7-O-beta-gentiobioside
CAS No. 88640-89-5
Chrysin 7-O-beta-gentiobioside( Chrysin 7-O-β-gentiobioside )
Catalog No. M28253 CAS No. 88640-89-5
Chrysin 7-O-beta-gentiobioside, a glycosylation product of Chrysin, is from Spartium junceum.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 205 | Get Quote |
![]() ![]() |
10MG | 329 | Get Quote |
![]() ![]() |
100MG | Get Quote | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameChrysin 7-O-beta-gentiobioside
-
NoteResearch use only, not for human use.
-
Brief DescriptionChrysin 7-O-beta-gentiobioside, a glycosylation product of Chrysin, is from Spartium junceum.
-
DescriptionChrysin 7-O-beta-gentiobioside, a glycosylation product of Chrysin, is from Spartium junceum.
-
In Vitro——
-
In Vivo——
-
SynonymsChrysin 7-O-β-gentiobioside
-
PathwayOthers
-
TargetOther Targets
-
RecptorCOX
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number88640-89-5
-
Formula Weight578.52
-
Molecular FormulaC27H30O14
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOC[C@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3cc(O)c4c(c3)oc(cc4=O)-c3ccccc3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Obach RS, et al. In vitro metabolism and covalent binding of enol-carboxamide derivatives and anti-inflammatory agents sudoxicam and meloxicam: insights into the hepatotoxicity of sudoxicam. Chem Res Toxicol. 2008 Sep;21(9):1890-9.
molnova catalog



related products
-
EZH2-IN-13
EZH2-IN-13, a potent EZH2 inhibitor, exhibits potential anticancer activity and may be utilized to study diseases associated with EZH2 activity.
-
Benzoylaconitine
Benzoylaconine is an alkaloid in the Chinese traditional medicine Radix Aconiti Lateralis Preparata (Fuzi). Benzoylaconine and aconitine can induce reproductive toxicity in BeWo Cell the amino acid metabolism was the main metabolic pathway and responsible for the placental and fetal toxicity of them.
-
Fmoc-D-Thr(Po(Obzl)O...
——