[CAS NO. 7085-55-4]  Troxerutin

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PRODUCTS SPECIFICATIONS [7085-55-4]

Store
Catalog
HY-N0139
Brand
MCE
CAS
7085-55-4

DESCRIPTION [7085-55-4]

Overview

MDLMFCD00893813
Molecular Weight742.68
Molecular FormulaC33H42O19
SMILESO=C1C(O[C@H]2[C@@H]([C@H]([C@@H]([C@@H](CO[C@H]3[C@@H]([C@@H]([C@H]([C@H](C)O3)O)O)O)O2)O)O)O)=C(C4=CC=C(OCCO)C(OCCO)=C4)OC5=CC(OCCO)=CC(O)=C15

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

1 Publications Citing Use of MCE


Summary

Troxerutin, also known as vitamin P4, is a tri-hydroxyethylated derivative of natural bioflavonoid rutins which can inhibit the production of reactive oxygen species ( ROS ) and depress ER stress-mediated NOD activation.


IC50 & Target

ROS [1] , NOD [2]


In Vitro

The results reveal that the maximum protective effect against ROS induced cell damage in the HDP cells occurs following pretreatment with 10 μM Troxerutin. Treatment with H 2 O 2 alone decreases cell viability to 77.33±2.44%; however, pretreatment with 10 μM Troxerutin maintains cell viability at 90.88±2.24% following H 2 O 2 exposure (P<0.05). At concentrations of 5 and 10 μM, pretreatment with Troxerutin causes a decrease in the number of cells in the sub G1 phase, indicative of cell death. In the control and Troxerutin-only-treated cells, 3.58±0.15 and 0.89±0.11% are 2′7′-dichlorofluorescein (DCF)-positive (P<0.05), whereas treatment with H 2 O 2 alone increases the level of ROS to 46.36±2.33%. The cells pretreated with Troxerutin are 19.92±1.95% DCF-positive following H 2 O 2 treatment, indicating that Troxerutin reduces the H 2 O 2 -induced production of ROS in the HDP cells [1] .

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


In Vivo

Troxerutin effectively lowers body weight and obesity-related metabolic parameters in high-fat diet (HFD)-treated mice. Oral administration of Troxerutin notably inhibits those liver injuries in HFD-treated mice, restores glucose intolerance and insulin signaling, and diminishes hepatic gluconeogenesis in HFD-treated mice. Troxerutin remarkably inhibits the nuclear translocation of NF-κB p65, as well as the expressions of its target genes, in the livers of HFD-treated mice. Troxerutin also depresses endoplasmic reticulum (ER) stress-mediated Nucleotide oligomerization domain (NOD) activation in HFD-treated mouse livers [2] . Lipid depositions in tunica intimae and tunica media are attenuated in Troxerutin-treated diabetic rats compare with untreated diabetic rats. Structural disarrangement and deformity of smooth muscle cells in aortic tissue of Troxerutin-treated diabetic rats are considerably lower than histology of untreated diabetic aorta. Administration of Troxerutin for four weeks to diabetic rats significantly reduces the level of malondialdehyde (MDA) compare to that of untreated diabetic rats (P<0.01) [3] .

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


Appearance

Solid



Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL ( 134.65 mM ; Need ultrasonic and warming)

H 2 O : ≥ 50 mg/mL ( 67.32 mM )

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.3465 mL 6.7324 mL 13.4647 mL
5 mM 0.2693 mL 1.3465 mL 2.6930 mL
10 mM 0.1346 mL 0.6732 mL 1.3465 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 0.5% CMC-Na /saline water

    Solubility: 24 mg/mL (32.32 mM); Clear solution; Need ultrasonic

  • 2.

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

    Solubility: ≥ 2.5 mg/mL (3.37 mM); Clear solution

  • 3.

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

    Solubility: ≥ 2.5 mg/mL (3.37 mM); Clear solution

  • 4.

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

    Solubility: ≥ 2.5 mg/mL (3.37 mM); Clear solution

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


Synonyms

4H-1-Benzopyran-4-one, 2-[3,4-bis(2-hydroxyethoxy)phenyl]-3-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-7-(2-hydroxyethoxy)-
Flavone, 3,5-dihydroxy-3′,4′,7-tris(2-hydroxyethoxy)-, 3-[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside]
2-[3,4-Bis(2-hydroxyethoxy)phenyl]-3-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-7-(2-hydroxyethoxy)-4H-1-benzopyran-4-one
3′,4′,7-Tris(hydroxyethyl)rutin
Troxerutin
Vitamin P4
Z 6000
3,5-Dihydroxy-3′,4′,7-tris(2-hydroxyethoxy)flavone 3-rutinoside
3′,4′,7-Tri-O-(β-hydroxyethyl)rutoside
Tris(hydroxyethyl)rutoside
Venoruton P4
Tris-O-(β-hydroxyethyl)rutoside
Factor P-Zyma
Rufen-P4
Tris(hydroxyethyl)rutin
Tris-O-(2-hydroxyethyl)rutin
TriHER
Troxerutine
Ruven
Vastribil
THR
Trioxyethylrutin
Veinamitol
Veniten
Posorutin
Troxevazin