5-Hydroxy-7-acetoxy-8-methoxyflavone
CAS No. 95480-80-1
5-Hydroxy-7-acetoxy-8-methoxyflavone( —— )
Catalog No. M37757 CAS No. 95480-80-1
5-Hydroxy-7-acetoxy-8-methoxyflavone is a flavonoid compound that inhibits lipid peroxidation and may exhibit anti-influenza virus activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 599 | In Stock |
|
| 5MG | 589 | In Stock |
|
| 10MG | 838 | In Stock |
|
| 25MG | 1264 | In Stock |
|
| 50MG | 1655 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name5-Hydroxy-7-acetoxy-8-methoxyflavone
-
NoteResearch use only, not for human use.
-
Brief Description5-Hydroxy-7-acetoxy-8-methoxyflavone is a flavonoid compound that inhibits lipid peroxidation and may exhibit anti-influenza virus activity.
-
Description5-Hydroxy-7-acetoxy-8-methoxyflavone (compound F24) is a flavone.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayImmunology/Inflammation
-
TargetAntiviral
-
RecptorAntiviral | Histone Demethylase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number95480-80-1
-
Formula Weight326.3
-
Molecular FormulaC18H14O6
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO(C)C1=C2C(=C(O)C=C1OC(C)=O)C(=O)C=C(O2)C3=CC=CC=C3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. T Nagai, et al. Inhibition of mouse liver sialidase by plant flavonoids. Biochem Biophys Res Commun. 1989 Aug 30;163(1):25-31.?
molnova catalog
related products
-
Cathepsin Inhibitor ...
Cathepsin Inhibitor 1 is an inhibitor of Cathepsin (L, L2, S, K, B) with pIC50 of 7.9, 6.7, 6.0, 5.5 and 5.2, respectively.
-
Tenofovir exalidex
Tenofovir exalidex (CMX 157) is a lipid-conjugated acyclic nucleotide analog of Tenofovir, demonstrating efficacy against wild-type and antiretroviral-resistant HIV strains, including those resistant to multiple nucleoside/nucleotide analogs.
-
Arg-AMS
Arg-AMS is an arginine tRNA synthetase inhibitor with antiviral activity that targets the host protein CD163 to inhibit porcine blue ear virus and the highly pathogenic strain HP-PRRSV, and can be used to study viral infections and myeloma.
Cart
sales@molnova.com