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UVI 3003

Cat. No. 3303 4 Citations Submit a Review Datasheet / COA / SDS
Pricing Availability   Qty
Description: RXR antagonist
Chemical Name: 3-[4-Hydroxy-3-[5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-3-(pentyloxy)-2-naphthalenyl]phenyl]-2-propenoic acid
Purity: ≥98% (HPLC)
Datasheet
Citations (4)
Reviews
Literature (3)
Biological Activity Technical Data Solubility Calculators Datasheets References

Biological Activity for UVI 3003

UVI 3003 is a RXR antagonist; displays high RXR binding affinity. Does not affect the corepressor interaction capacity of the RARα subunit within the context of the RAR-RXR heterodimer.

Technical Data for UVI 3003

M. Wt 436.58
Formula C28H36O4
Storage Store at -20°C
Purity ≥98% (HPLC)
CAS Number 847239-17-2
PubChem ID 44566108
InChI Key APJSHECCIRQQDV-ZRDIBKRKSA-N
Smiles CC1(C)C2=C(C=C(C3=C(O)C=CC(/C=C/C(O)=O)=C3)C(OCCCCC)=C2)C(C)(C)CC1

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Solubility Data for UVI 3003

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 43.66 100
ethanol 43.66 100

Preparing Stock Solutions for UVI 3003

The following data is based on the product molecular weight 436.58. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 2.29 mL 11.45 mL 22.91 mL
5 mM 0.46 mL 2.29 mL 4.58 mL
10 mM 0.23 mL 1.15 mL 2.29 mL
50 mM 0.05 mL 0.23 mL 0.46 mL

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References for UVI 3003

References are publications that support the biological activity of the product.

Le Maire et al (2009) Activation of RXR-PPAR heterodimers by organotin environmental endocrine disruptors. EMBO Rep. 10 367 PMID: 19270714

Santin et al (2009) Modulating retinoid X receptor with a series of (E)-3-[4-Hydroxy-3-(3-alkoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)phenyl]acrylic acids and their 4-alkoxy isomers. J.Med.Chem. 52 3150 PMID: 19408900

Nahoum et al (2007) Modulators of the stuctural dynamics of the retinoid X receptor to reveal receptor function. Proc.Natl.Acad.Sci. 104 17323

If you know of a relevant reference for UVI 3003, please let us know.

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Keywords: UVI 3003, UVI 3003 supplier, UVI3003, rxr, retinoid, x, receptors, antagonists, Retinoid, X, Receptor, 3303, Tocris Bioscience

4 Citations for UVI 3003

Citations are publications that use Tocris products. Selected citations for UVI 3003 include:

Porcu et al (2015) Clobetasol and halcin. Act as Smoothened Agonists to Promote Myelin Gene Expression and RxRγ Receptor Activation. PLoS One 10 e0144550 PMID: 26658258

Hebert (2017) Effects of retinoic acid signaling on extraocular muscle myogenic precursor cells in vitro. Exp Cell Res 361 101 PMID: 29017757

Cambray et al (2012) AVNinduces cortical interneuron identity and differentiation in embryonic stem cell-derived telencephalic neural precursors. Nat Commun 3 841 PMID: 22588303

Marconett et al (2013) Integrated transcriptomic and epigenomic analysis of primary human lung epithelial cell differentiation. PLoS Genet 9 e1003513 PMID: 23818859

Do you know of a great paper that uses UVI 3003 from Tocris? Please let us know.

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