Dihydromyricetin
CAS No. 27200-12-0
Dihydromyricetin( Ampelopsin | Ampeloptin )
Catalog No. M18341 CAS No. 27200-12-0
Dihydromyricetin is a potent inhibitor of dihydropyrimidinase with an IC50 of 48 μM. Dihydromyricetin can activate autophagy by inhibiting mTOR signaling.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 41 | In Stock |
|
| 5MG | 37 | In Stock |
|
| 10MG | 52 | In Stock |
|
| 25MG | 69 | In Stock |
|
| 50MG | 83 | In Stock |
|
| 100MG | 129 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 322 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDihydromyricetin
-
NoteResearch use only, not for human use.
-
Brief DescriptionDihydromyricetin is a potent inhibitor of dihydropyrimidinase with an IC50 of 48 μM. Dihydromyricetin can activate autophagy by inhibiting mTOR signaling.
-
DescriptionAmpelopsin, also known as dihydromyricetin, is a type of flavonoid. It can be found in Cedrus deodara or in the Japanese raisin tree (Hovenia dulcis). It is also found in Erythrophleum africanum. The compound is credited with hepatoprotective effects observed in rodents. Use of Hovenia species in traditional Chinese herbal medicine as a hangover cure has led to research into the potential action of dihydromyricetin in counteracting the effects of alcohol in the brain.
-
In Vitro——
-
In Vivo——
-
SynonymsAmpelopsin | Ampeloptin
-
PathwayOthers
-
TargetOther Targets
-
RecptorGABAR
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number27200-12-0
-
Formula Weight320.25
-
Molecular FormulaC15H12O8
-
Purity>98% (HPLC)
-
SolubilityDMSO : ≥ 100 mg/mL; 312.26 mM
-
SMILESC1=C(C=C(C(=C1O)O)O)[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O
-
Chemical Name(2R,3R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
L524-0366
L524-0366 is a TWEAK-Fn14 signaling cascade inhibitor.L524-0366 mitigated maladaptive remodeling with TAC. TWEAK induced secretion of the pro-inflammatory chemokine, monocyte chemoattractant protein 1 from WT but not Fn14-/-?fibroblasts in vitro, in part through activation of non-canonical NF-κB signaling.
-
P-SCN-Bn-DOTA
p-SCN-Bn-DOTA is a chelator that simultaneously binds radionuclides and links monoclonal antibodies.
-
D-tetrahydropalmatin...
D-Tetrahydropalmatine is a organic cation transporter 1 (OCT1) inhibitor it can obviously inhibit the uptake of monocrotaline (MCT) in MDCK-hOCT1 cells and isolate rat primary hepatocytes and attenuate the viability reduction and LDH release of the primary cultured rat hepatocytes caused by MCT.
Cart
sales@molnova.com