[CAS NO. 55986-43-1]  Cetaben

Ships within Stock Price Qty Total
$0.00
$0.00
Please click "REQUEST A QUOTE" button if you need other sizes or custom synthesis
request a quote
If there is no stock, or you need other sizes or custom synthesis, please:

PRODUCTS SPECIFICATIONS [55986-43-1]

Fulfillment
Catalog
AS938671
Brand
Arctom Scientific
CAS
55986-43-1

DESCRIPTION [55986-43-1]

Overview

MDLMFCD00865766
Molecular Weight361.56
Molecular FormulaC23H39NO2
SMILESO=C(C1=CC=C(C=C1)NCCCCCCCCCCCCCCCC)O

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

Summary

Cetaben is a PPARα-independent peroxisome proliferator. Cetaben is a non-fibrate hypolipidemic drug and potently reduces the concentration of cholesterol and triglycerides [1] [2] .


In Vitro

Cetaben (10 µM; 24 hours) induces severe micromorphological and ultrastructural changes in HepG2 and MH1C1 cells. After treatment with 100 µM cetaben, cells contained several Golgi regions, most of them disintegrated into vesicles [2] .
Cetaben-treated (10 µM; 24 hours) cells were characterized by a striking heterogeneity of the peroxisomal population with the occurrence of dumbbell-shaped and cup-shaped peroxisomal profiles in MH1C1cells [2] .

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


In Vivo

Cetaben reveales a significant rise in the activities of peroxisomal enzymes in both the liver and kidney at doses of 50-100 mg/kg body over 10 days, but the maximal effect is observed at 250 mg/kg [1] .

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

Animal Model: Male Wistar rats [1]
Dosage: 10,25,50,100,250 and 500 mg/kg
Administration: Gavage; 10 day
Result: Revealed a significant rise in the activities of peroxisomal enzymes in both the liver and kidney at doses of 50-100 mg/kg body over 10 days, but the maximal effect was observed at 250 mg/kg.

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

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

Solvent & Solubility

In Vitro:

DMSO : 10 mg/mL ( 27.66 mM ; ultrasonic and warming and heat to 60°C)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.7658 mL 13.8290 mL 27.6579 mL
5 mM 0.5532 mL 2.7658 mL 5.5316 mL
10 mM 0.2766 mL 1.3829 mL 2.7658 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 (6.91 mM); Clear solution; Need ultrasonic

  • 2.

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

    Solubility: ≥ 2.5 mg/mL (6.91 mM); Clear solution

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


Synonyms

Benzoic acid, 4-(hexadecylamino)-
4-(Hexadecylamino)benzoic acid
Cetaben
4-(n-Hexadecylamino)benzoic acid