[CAS NO. 847239-17-2]  UVI 3003

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PRODUCTS SPECIFICATIONS [847239-17-2]

Catalog
HY-107500
Brand
MCE
CAS
847239-17-2

DESCRIPTION [847239-17-2]

Overview

MDLMFCD18086862
Molecular Weight436.58
Molecular FormulaC28H36O4
SMILESCCCCCOC1=C(C2=CC(/C=C/C(O)=O)=CC=C2O)C=C3C(C(C)(CCC3(C)C)C)=C1

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


Summary

UVI 3003 is a highly selective antagonist of retinoid X receptor (RXR) , and inhibits xenopus and human RXRα in Cos7 cells, with IC 50 s of 0.22 and 0.24 μM, respectively.


IC50 & Target

IC50: 0.22 μM (Xenopus RXRα, in Cos7 cells), 0.24 μM (Human RXRα, in Cos7 cells) [1]


In Vitro

UVI3003 inhibits the activity of xenopus and human RXRα, with IC 50 s of 0.22 and 0.24 μM, respectively. UVI3003 fully activates xPPARγ with an EC 50 of 12.6 μM, and is almost completely inactive on hPPARγ and mPPARγ [1] . UVI 3003 (10 μM) does not change the proliferation rate of extraocular muscles (EOM)-derived or LEG-derived EECD34 cells. UVI 3003 causes a 65.4% difference in EECD34 cell fusion and desmin expression [2] .

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 ( 229.05 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.2905 mL 11.4527 mL 22.9053 mL
5 mM 0.4581 mL 2.2905 mL 4.5811 mL
10 mM 0.2291 mL 1.1453 mL 2.2905 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 (5.73 mM); Clear solution

  • 2.

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

    Solubility: ≥ 2.5 mg/mL (5.73 mM); Clear solution

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