Introduction:Basic information about CAS 28500-04-1|Malvidin-3-O-arabinoside chloride, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Malvidin-3-O-arabinoside chloride |
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| CAS Number | 28500-04-1 | Molecular Weight | 498.864 |
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| Density | / | Boiling Point | / |
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| Molecular Formula | C22H23O11.Cl | Melting Point | / |
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| MSDS | / | Flash Point | / |
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Names
| Name | Malvidin-3-O-arabinoside chloride |
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| Synonym | More Synonyms |
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Malvidin-3-O-arabinoside chloride BiologicalActivity
| Description | Malvidin-3-O-arabinoside chloride ameliorates ethyl carbamate-induced oxidative damage by stimulating AMPK-mediated autophagy[1]. |
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| Related Catalog | Signaling Pathways >>Epigenetics >>AMPKSignaling Pathways >>Autophagy >>AutophagyResearch Areas >>Inflammation/ImmunologySignaling Pathways >>PI3K/Akt/mTOR >>AMPKResearch Areas >>Metabolic Disease |
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| In Vitro | Malvidin-3-O-arabinoside chloride (M3A chloride, 50-400 μM) pretreatment remarkably upregulates LAMP-1 expression, which indicates elevated lysosomal mass. M3A also successfully restores lysosomal acidity and subsequently strengthenes lysosomal functions. M3A stimulates phosphorylation of AMP-activated protein kinase (AMPK), a master regulator of autophagy[1]. Cell Autophagy Assay[1] Cell Line: Caco-2 cell line. Concentration: 50, 100, 200 and 400 μM. Incubation Time: 24 h (then treated with or without 10 μM chloroquine (CQ) for another 1 h). Result: Notably inhibited excess ROS generation. 200 μM and 400 μM M3A pretreatment significantly enhanced 14% and 16% of GSH level. Enhanced autophagy flux. Significantly up-regulate the LC3-II/LC3-I ratio. |
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| References | [1]. Yuting Li, et al. Malvidin-3-O-arabinoside ameliorates ethyl carbamate-induced oxidative damage by stimulating AMPK-mediated autophagy. Food Funct. 2020 Dec 1;11(12):10317-10328. |
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Chemical & Physical Properties
| Molecular Formula | C22H23O11.Cl |
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| Molecular Weight | 498.864 |
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| Exact Mass | 498.092896 |
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Synonyms
| 5,7-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-chromeniumyl D-arabinopyranoside chloride |
| D-Arabinopyranoside, 5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-1-benzopyrylium-3-yl, chloride (1:1) |