Cart
sales@molnova.com
4-O-Methylpyridoxine
CAS No. 1464-33-1
4-O-Methylpyridoxine( —— )
Catalog No. M37811 CAS No. 1464-33-1
4'-O-Methylpyridoxine (MPN) is a vitamin-like compound discovered from Ginkgo biloba with antioxidant activity and cytotoxicity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 49 | In Stock |
|
| 5MG | 46 | In Stock |
|
| 10MG | 68 | In Stock |
|
| 25MG | 112 | In Stock |
|
| 50MG | 164 | In Stock |
|
| 100MG | 244 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 593 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name4-O-Methylpyridoxine
-
NoteResearch use only, not for human use.
-
Brief Description4'-O-Methylpyridoxine (MPN) is a vitamin-like compound discovered from Ginkgo biloba with antioxidant activity and cytotoxicity.
-
Description4'-O-Methylpyridoxine, a natural compound, possesses antioxidant activity.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetAntioxidant
-
RecptorAntioxidant
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1464-33-1
-
Formula Weight183.2
-
Molecular FormulaC9H13NO3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (545.85 mM; Ultrasonic )
-
SMILESCOCc1c(CO)cnc(C)c1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Isaac Duah Boateng, et al. Effect of different drying methods on product quality, bioactive and toxic components of Ginkgo biloba L. seed. J Sci Food Agric. 2021 Jun;101(8):3290-3297.?
molnova catalog
related products
-
4-Hydroxyquinoline
4-Hydroxyquinoline is a hydroxylated quinoline derivative with antimicrobial activity.
-
Adrenochrome
Adrenochrome (Adraxone) is a cytotoxic molecule that can be used to kill bacteria. Adrenochrome is an oxidized product of Epinephrine.
-
CFSE
Carboxyfluorescein succinimidyl ester (CFSE) is a fluorescent cell staining dye. CFSE is cell permeable and covalently couples, via its succinimidyl group, to intracellular molecules, notably, to intracellular lysine residues and other amine sources.
