Cart
sales@molnova.com
Tetrahydroamentoflavone
CAS No. 48236-96-0
Tetrahydroamentoflavone( —— )
Catalog No. M29347 CAS No. 48236-96-0
Tetrahydroamentoflavone is a potent XO inhibitor (IC50 = 92 nM, Ki = 982 nM) with anti-inflammatory effects. Tetrahydroamentoflavone can be used for studies about inflammation and gout.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameTetrahydroamentoflavone
-
NoteResearch use only, not for human use.
-
Brief DescriptionTetrahydroamentoflavone is a potent XO inhibitor (IC50 = 92 nM, Ki = 982 nM) with anti-inflammatory effects. Tetrahydroamentoflavone can be used for studies about inflammation and gout.
-
DescriptionTetrahydroamentoflavone is a potent XO inhibitor (IC50 = 92 nM, Ki = 982 nM) with anti-inflammatory effects. Tetrahydroamentoflavone can be used for studies about inflammation and gout.(In Vitro):Tetrahydroamentoflavone shows in vitro cyclooxygenase (COX) inhibition activity with an IC50 of 29.5 microM for COX-1 and 40.5% inhibition at 100 microg/mL for COX-2.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayChromatin/Epigenetic
-
TargetCOX
-
RecptorCOX
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number48236-96-0
-
Formula Weight542.5
-
Molecular FormulaC30H22O10
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOc1ccc(cc1)[C@@H]1CC(=O)c2c(O)cc(O)c(c2O1)-c1cc(ccc1O)[C@@H]1CC(=O)c2c(O)cc(O)cc2O1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
STYLOPINE
(-)-STYLOPINE is a natural product from Chelidonium majus L.
-
Suxibuzone
Suxibuzone is a drug used for joint and muscular pain. It is a prodrug of the non steroidal anti inflammatory drug phenylbutazone, and is commonly used in horses.
-
DuP-697
DuP-697 is an irreversible, specific COX-2 inhibitor with IC50 values ??of 10 nM and 800 nM for human COX-2 and COX-1. DuP-697 also exhibits anti-angiogenic, anti-inflammatory, antipyretic and apoptotic effects.
