A retinoid
Related Products
Labeled Version(s)
28696Acitretin-d3
Parent Compound(s)
19878Etretinate
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Acitretin

Item No. 20853

Technical Information
Formal Name
(2E,4E,6E,8E)-9-(4-methoxy-2,3,6-trimethylphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoic acid
CAS Number
55079-83-9
Synonyms
  • all-trans Acitretin
  • Ro 10-1670
  • Ro 10-1670/000
Molecular Formula
C21H26O3
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 5 mg/mlDMF:PBS (pH 7.2) (1:4): 0.2 mg/mlDMSO: 1 mg/ml
λmax
357 nm
SMILES
CC1=C(OC)C=C(C)C(/C=C/C(C)=C/C=C/C(C)=C/C(O)=O)=C1C
InChi Code
InChI=1S/C21H26O3/c1-14(8-7-9-15(2)12-21(22)23)10-11-19-16(3)13-20(24-6)18(5)17(19)4/h7-13H,1-6H3,(H,22,23)/b9-7+,11-10+,14-8+,15-12+
InChi Key
IHUNBGSDBOWDMA-AQFIFDHZSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Lipid Resource Center
    Discover Products & Resources for Lipid Research
    • High-purity lipid standards
    • Lipid roles in biology
    • Lipids in health & disease
    • Lipids for pharmaceutical development
    • Protocols, advice, & resources
    EXPLORE NOW
    Product Description

    Acitretin is a retinoid and an active metabolite of the retinoid etretinate (Item No. 19878) that has antiproliferative activities.1,2 It binds to cellular retinoic acid binding protein I (CRABP-I) and CRABP-II (Kds = 3 and 15 nM, respectively, for the mouse recombinant proteins) but has low affinity for human recombinant retinoic acid receptor-retinoid X receptor (RAR-RXR) heterocomplexes.3,4 Acitretin inhibits proliferation (IC50 = 6.6 µM) and suppresses TNF-α- and IFN-γ-induced protein levels of STAT1, NF-ĸB, and RANTES in HaCaT keratinocytes when used at concentrations up to 50 µM.5 It inhibits proliferation of HL-60, SCC4, SCC15, and A431, but not MCF-7, cancer cells, when used at a concentration of 30 µM.2 Acitretin (20 µg per mouse) decreases the severity of psoriatic-like skin lesions in K14-VEGF transgenic mice.1 Formulations containing acitretin have been used in the treatment of psoriasis.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. An, J., Zhang, D., Wu, J., et alThe acitretin and methotrexate combination therapy for psoriasis vulgaris achieves higher effectiveness and less liver fibrosis. Pharmacol. Res. 121, 158-168 (2017).

    2. Frey, J.R., Peck, R., and Bollag, W. Antiproliferative activity of retinoids, interferon α and their combination in five human transformed cell lines. Cancer Lett. 57(3), 223-227 (1991).

    3. Norris, A.W., Cheng, L., Giguère, V., et alMeasurement of subnanomolar retinoic acid binding affinities for cellular retinoic acid binding proteins by fluorometric titration. Biochim. Biophys. Acta 1209(1), 10-18 (1994).

    4. Tian, K., Norris, A.W., Lin, C.L., et alThe isolation and characterization of purified heterocomplexes of recombinant retinoic acid receptor and retinoid X receptor ligand binding domains. Biochemistry 36(19), 5669-5676 (1997).

    5. Zhang, M., Zhu, L., Feng, Y., et alEffects of acitretin on proliferative inhibition and RANTES production of HaCaT cells. Arch. Dermatol. Res. 300(10), 575-581 (2008).