CAS 535-96-6
:Marein
Description:
Marein, with the CAS number 535-96-6, is a chemical compound that belongs to the class of flavonoids, specifically a type of flavonol glycoside. It is primarily derived from various plant sources, particularly those in the genus *Morus*, such as mulberries. Marein is characterized by its glycosidic structure, which consists of a flavonol backbone attached to a sugar moiety. This compound exhibits a range of biological activities, including antioxidant, anti-inflammatory, and potential anticancer properties, making it of interest in pharmacological research. Additionally, marein is known for its solubility in polar solvents, which can influence its bioavailability and efficacy in biological systems. Its presence in natural products contributes to the health benefits associated with the consumption of certain fruits and plants. As with many flavonoids, marein may also play a role in plant pigmentation and UV protection. Further studies are ongoing to fully elucidate its mechanisms of action and potential therapeutic applications.
Formula:C21H22O11
InChI:InChI=1S/C21H22O11/c22-8-15-18(28)19(29)20(30)21(32-15)31-14-6-3-10(16(26)17(14)27)11(23)4-1-9-2-5-12(24)13(25)7-9/h1-7,15,18-22,24-30H,8H2/b4-1+/t15-,18-,19+,20-,21-/m1/s1
InChI key:InChIKey=XGEYXJDOVMEJNG-HTFDPZBKSA-N
SMILES:O([C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C2=C(O)C(O)=C(C(/C=C/C3=CC(O)=C(O)C=C3)=O)C=C2
Synonyms:- (2E)-3-(3,4-Dihydroxyphenyl)-1-[4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-2,3-dihydroxyphenyl]-2-propen-1-one
- (E)-3-(3,4-Dihydroxyphenyl)-1-(4-(beta-D-glucopyranosyloxy)-2,3-dihydroxyphenyl)-2-propen-1-one
- 2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(4-(beta-D-glucopyranosyloxy)-2,3-dihydroxyphenyl)-, (E)-
- 2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-[4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-2,3-dihydroxyphenyl]-, (2E)-
- 2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-[4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-2,3-dihydroxyphenyl]-, (E)-
- 4-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenyl beta-D-glucopyranoside
- Chalcone, 2′,3,3′,4,4′-pentahydroxy-, 4′-β-<span class="text-smallcaps">D</span>-glucopyranoside
- Glucopyranoside, okanin-4′, β-<span class="text-smallcaps">D</span>-
- Marein
- Okanin 4′-O-β-<span class="text-smallcaps">D</span>-Glucopyranoside
- Okanin-4'-O-glucoside
- 2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-[4-(β-D-glucopyranosyloxy)-2,3-dihydroxyphenyl]-, (2E)-
- (2E)-3-(3,4-Dihydroxyphenyl)-1-[4-(β-D-glucopyranosyloxy)-2,3-dihydroxyphenyl]-2-propen-1-one
- 2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-[4-(β-D-glucopyranosyloxy)-2,3-dihydroxyphenyl]-, (E)-
- See more synonyms
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Found 9 products.
Marein
CAS:Marein analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C21H22O11Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:450.4Marein
CAS:Marein shows neuroprotective effect on PC12 cell damage induced by methylglyoxal, which is due to a reduction of damage to mitochondria function and activation of the AMPK signal pathway, it may be a potent compound for preventing/counteracting diabetic encephalopathy. Marein can improve insulin resistance induced by high glucose in HepG2 cells through CaMKK/AMPK/GLUT1 to promote glucose uptake, through IRS/Akt/GSK-3β to increase glycogen synthesis, and through Akt/FoxO1 to decrease gluconeogenesis. Marein shows antioxidant activity, it shows Histone deacetylase enzymes (HDACs) inhibitory activity and it also can inhibit TNFα-induced NF-κB activation.Formula:C21H22O11Purity:95%~99%Molecular weight:450.396Marein
CAS:Marein prevents PC12 cell damage by protecting mitochondria and activating AMPK, potentially countering diabetic encephalopathy.Formula:C21H22O11Purity:99.12% - 99.84%Color and Shape:SolidMolecular weight:450.39Marein
CAS:<p>Please enquire for more information about Marein including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C21H22O11Purity:Min. 95%Molecular weight:450.39 g/mol







