4-Hydroxyretinoic acid
Based on 1 publication(s) in Google Scholar
4-Hydroxyretinoic acid (4-HRA) is a derivative of Retinoic acid (HY-14649). 4-Hydroxyretinoic acid is formed via the catalysis of retinol by cytochrome P-450 isoenzymes. 4-Hydroxyretinoic acid also serves as a substrate for UDP-glucuronosyltransferase (s) and recombinant UGT2B7. 4-Hydroxyretinoic acid binds to the nuclear receptor RAR (Retinoic Acid Receptor), activates RAR and RXR-alpha, subsequently regulates gene expression and cell differentiation, and induces cancer cell apoptosis (Apoptosis). 4-Hydroxyretinoic acid also participates in multiple physiological processes such as immunoregulation, neuroprotection and antioxidation.
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- Pureté: 94.58%
- CAS No.: 66592-72-1
- Formule: C20H28O3
- Masse moléculaire:316.43
-
Stockage:
-80°C, protect from light, stored under nitrogen
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Activité biologique
-
Chemical Information
- Pureté et documentation
- Références
-
Help & FAQs
Publications Citing Use of MedChemExpress (MCE) 4-Hydroxyretinoic acid
More
Activité biologique
|
UGT2B7 |
4-Hydroxyretinoic acid (10-11-5×10-4 M) stimulates RAR-β, RAR-γ, RAR-α, and RXR-α mediated transcription of the TRE3-tk-CAT reporter gene in cotransfected CV-1 cells with ED50 values of 75 nM, 30 nM, >500 nM, and >500 nM, respectively[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 66592-72-1
-
Appearance Solid
-
Masse moléculaire 316.43
-
Formule C20H28O3
-
Color White to yellow
-
SMILES
CC(/C=C/C=C(/C=C/C1=C(C(O)CCC(C)1C)C)C)=C\C(O)=O
-
Livraison
Shipping with dry ice.
-
Stockage
-80°C, protect from light, stored under nitrogen
Publications (1)
-
Journal Impact Factor
-
Most Recent
-
J Biol Chem
A cell-based assay for retinaldehyde dehydrogenase activity: Retinoid quantification as an alternative to current fluorescence-based approaches. [Abstract]2026 Jan 29;302(3):111211. PMID: 41617028
Pureté et documentation
-
Fiche technique (269 KB)
-
SDS (701 KB)
- English - EN (701 KB)
- Français - FR (701 KB)
- Deutsch - DE (701 KB)
- Norwegian - NO (701 KB)
- Español - ES (701 KB)
- Swedish - SV (701 KB)
- Italian - IT (701 KB)
- Korean - KR (701 KB)
- Portuguese - PT (701 KB)
-
Instruction de manipulation (2659 KB)
Références
[1]. Samokyszyn VM, et al. 4-hydroxyretinoic acid, a novel substrate for human liver microsomal UDP-glucuronosyltransferase(s) and recombinant UGT2B7. J Biol Chem. 2000;275(10):6908-6914. [Content Brief]
[2]. Duell EA, et al. Human skin levels of retinoic acid and cytochrome P-450-derived 4-hydroxyretinoic acid after topical application of retinoic acid in vivo compared to concentrations required to stimulate retinoic acid receptor-mediated transcription in vitro. J Clin Invest. 1992;90(4):1269-1274. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
4-Hydroxyretinoic acid Related Classifications
HY-125904 Related Classifications
Powered by Bioz