2,3-Dihydroxy-4-methoxyacetophenone
CAS No. 708-53-2
2,3-Dihydroxy-4-methoxyacetophenone( —— )
Catalog No. M24722 CAS No. 708-53-2
2,3-Dihydroxy-4-methoxyacetophenone is a natural product,it improves cognitive function and may be helpful for the treatment of Alzheimer's disease.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 38 | In Stock |
|
| 100MG | 52 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name2,3-Dihydroxy-4-methoxyacetophenone
-
NoteResearch use only, not for human use.
-
Brief Description2,3-Dihydroxy-4-methoxyacetophenone is a natural product,it improves cognitive function and may be helpful for the treatment of Alzheimer's disease.
-
Description2,3-Dihydroxy-4-methoxyacetophenone is a natural product,it improves cognitive function and may be helpful for the treatment of Alzheimer's disease.
-
In Vitro2,3-Dihydroxy-4-methoxyacetophenone protects HT22 cells on glutamate induced cell-death in a dose-dependent manner (EC50=10.94 μM). 2,3-Dihydroxy-4-methoxyacetophenone inhibits [Ca2+] accumulation in HT22 cells and has antioxidantive activity.
-
In Vivo2,3-dihydroxy-4-methoxyacetophenone (50mg/kg; po) improves the impairment of spatial memory induced by scopolamine.
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetCalcium Channel
-
RecptorCalcium Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number708-53-2
-
Formula Weight182.17
-
Molecular FormulaC9H10O4
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESCC(C1=CC=C(OC)C(O)=C1O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.The ameliorating effects of 2,3-dihydroxy-4-methoxyacetophenone on scopolamine-induced memory impairment in mice and its neuroprotective activity. Bioorg Med Chem Lett. 2013 Dec 15;23(24):6732-6.
molnova catalog
related products
-
Bay K-8644
Bay K-8644 is a potent L-type calcium channels (LTCCs) activator with EC50 of 17.3 nM.
-
TTA-A8
TTA-A8 is an antagonist of T-type calcium channel.
-
SNX 482
Potent and selective, voltage-dependent R-type CaV2.3 calcium channel blocker (IC50 = 30 nM). Antinociceptive; inhibits nociceptive C-fibre and Aδ-fibre-evoked neuronal responses.
Cart
sales@molnova.com