[CAS NO. 535-96-6]  Marein

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PRODUCTS SPECIFICATIONS [535-96-6]

Catalog
HY-N7676
Brand
MCE
CAS
535-96-6

DESCRIPTION [535-96-6]

Overview

MDL-
Molecular Weight450.39
Molecular FormulaC21H22O11
SMILESO=C(C1=CC=C(O[C@H]2[C@@H]([C@H]([C@@H]([C@@H](CO)O2)O)O)O)C(O)=C1O)/C=C/C3=CC=C(O)C(O)=C3

For research use only. We do not sell to patients.

Summary

Marein has the neuroprotective effect due to a reduction of damage to mitochondria function and activation of the AMPK signal pathway . Marein improves 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 is a HDAC inhibitor with an IC 50 of 100 µM. Marein has beneficial antioxidative, antihypertensive, antihyperlipidemic and antidiabetic effects [1] [2] [3] .


IC50 & Target

IC50: 100 µM (HDAC) [3]


In Vitro

Marein (0-1000 µM; 24 h) inhibits HDAC activity and TNFα-induced NF-κB activation with IC 50 values of 100 and >200 μM, respectively [1] .
Marein (1.25-40 μM; 24 h) promotes glucose uptake in HepG2 cells [2] .
Marein (5-10 μM; 24 h) promotes GLUT1 translocation from intercellular vesicles to the plasma membrane, increases hepatic glycogen content and down-regulates expression levels of G6Pase and PEPCK in HepG2 cells [2] .
Marein (5-10 μM; 24 h) stimulates 2-NBDG uptake, and it can be reduced by STO-609 and compound C which is a inhibitor of AMPK [2] .
Marein (0-40 μM; 24 h) affects the cytotoxicity of MG in PC12 cells [3] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis [2]

Cell Line: HepG2 cell line
Concentration: 5 and 10 μM
Incubation Time: 24 hours
Result: Increased GLUT1 translocation to plasma membrane and decreased the phosphorylation level of AS160 and GSK-3β in HepG2 cells.

Western Blot Analysis [2]

Cell Line: HepG2 cell line
Concentration: 10 μM
Incubation Time: 0-10 hours
Result: Time- and dose-dependently induced phosphorylation of AMPK and Akt in HepG2 cells.

Cell Viability Assay [3]

Cell Line: PC12 cell line
Concentration: 0-40 μM
Incubation Time: 24 hours
Result: Prevened MG-induced loss of viability in PC12 cells.

Apoptosis Analysis [3]

Cell Line: PC12 cell line
Concentration: 5-10 μM
Incubation Time: 30 min
Result: Protected PC12 cells from MG-induced apoptosis.

Western Blot Analysis [3]

Cell Line: PC12 cell line
Concentration: 5-10 μM
Incubation Time: 30 min
Result: Increased phospho-AMPKα (Thr172) in PC12 cells.

Appearance

Solid



Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)


Solvent & Solubility

In Vitro:

DMSO : 25 mg/mL ( 55.51 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.2203 mL 11.1015 mL 22.2030 mL
5 mM 0.4441 mL 2.2203 mL 4.4406 mL
10 mM 0.2220 mL 1.1101 mL 2.2203 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.5 mg/mL (5.55 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (5.55 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: 2.5 mg/mL (5.55 mM); Suspended solution; Need ultrasonic

* All of the co-solvents are available by MCE.


Synonyms

2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-[4-(β-D-glucopyranosyloxy)-2,3-dihydroxyphenyl]-, (2E)-
2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-[4-(β-D-glucopyranosyloxy)-2,3-dihydroxyphenyl]-, (E)-
Marein
Chalcone, 2′,3,3′,4,4′-pentahydroxy-, 4′-β-D-glucopyranoside
(2E)-3-(3,4-Dihydroxyphenyl)-1-[4-(β-D-glucopyranosyloxy)-2,3-dihydroxyphenyl]-2-propen-1-one
Glucopyranoside, okanin-4′, β-D-
Okanin 4′-O-β-D-Glucopyranoside