Home -
Products -
Others -
Other Targets -
Peonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside
Peonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside
CAS No. 863560-74-1
Peonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside( ——— )
Catalog No. M39757 CAS No. 863560-74-1
Peonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | Get Quote | Get Quote |
|
| 50MG | Get Quote | 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 NamePeonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside
-
NoteResearch use only, not for human use.
-
Brief DescriptionPeonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside
-
DescriptionPeonidin-3-O-(6-O-trans-feruloyl-2-O-β-glucopyranosyl-β-glucopyranoside)-5-O-β-glucopyranoside
-
In Vitro———
-
In Vivo———
-
Synonyms———
-
PathwayOthers
-
TargetOther Targets
-
Recptor———
-
Research Area———
-
Indication———
Chemical Information
-
CAS Number863560-74-1
-
Formula Weight———
-
Molecular Formula———
-
Purity>98% (HPLC)
-
Solubility———
-
SMILES———
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
ICI-118551 Hydrochlo...
ICI-118551 is a highly selective β2-adrenergic receptor antagonist with Ki values of 0.7, 49.5 and 611 nM for β2, β1 and β3 receptors, respectively.
-
Eschweilenol C
Eschweilenol C has antifungal, anti-inflammatory, antioxidant, antidiabetic activity.
-
Cirsimaritin
Cirsimaritin exhibits antibacterial, anti-inflammation, anti-tumor, antioxidant properties and renal protection. Cirsimaritin binds weakly to the benzodiazepine site on GABAA receptors.
Cart
sales@molnova.com