A β2-AR agonist
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.

Formoterol (hemifumarate hydrate)

Item No. 15584

Technical Information
Formal Name
rel-N-[2-hydroxy-5-[(1R)-1-hydroxy-2-[[(1R)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]-formamide, 2E-butenedioate (2:1), hydrate
Molecular Formula
C19H24N2O4 • 1/2C4H4O4 [XH2O]
Formula Weight
Purity
≥99%
A solid
DMSO: 20 mg/mlMethanol: 1 mg/mlWater: Slightly Soluble
λmax
215, 285 nm
SMILES
COC1=CC=C(C[C@H](C)NC[C@@H](O)C2=CC(NC([H])=O)=C(O)C=C2)C=C1.OC(/C=C/C(O)=O)=O.COC3=CC=C(C[C@H](C)NC[C@@H](O)C4=CC(NC([H])=O)=C(O)C=C4)C=C3.O
InChi Code
InChI=1S/2C19H24N2O4.C4H4O4.H2O/c2*1-13(9-14-3-6-16(25-2)7-4-14)20-11-19(24)15-5-8-18(23)17(10-15)21-12-22;5-3(6)1-2-4(7)8;/h2*3-8,10,12-13,19-20,23-24H,9,11H2,1-2H3,(H,21,22);1-2H,(H,5,6)(H,7,8);1H2/b;;2-1+;/t2*13-,19+;;/m00../s1
InChi Key
BPXZSHHCUKRDHD-PGVRECGZSA-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

    Cayman Chemical
    Visit Our Cancer Resource Center
    Find Tools & Resources to Study the Hallmarks of Cancer
    • Cancer cell signaling & regulation
    • Cancer metabolism
    • Tumor microenvironment
    EXPLORE NOW
    Product Description

    Formoterol is an agonist of the β2-adrenergic receptor (β2-AR).1 It induces cAMP efflux in, and relaxation of, rat tracheal rings precontracted with carbachol (carbamoylcholine; Item No. 14486) when used at a concentration of 1 µM.2 Aerosolized formoterol (10 µg/ml) prevents the late asthmatic response, reduces the number of eosinophils and macrophages in bronchoalveolar lavage fluid (BALF), and reduces bronchial reactivity in a guinea pig model of allergic asthma induced by ovalbumin.3 Formoterol is also an inhibitor of ferroptosis, preventing cell death induced by RSL-3 (Item No. 19288) or erastin (Item No. 17754) in HT-1080 human fibrosarcoma cells in a concentration-dependent manner.4 It scavenges lipid peroxyl radicals in oxidized egg phosphatidylcholine liposomes when used at concentrations ranging from 10 to 100 µM. Formoterol (1 and 5 mg/kg) reduces acute liver injury and hepatic lipid peroxidation induced by acetaminophen (Item No. 10024) in mice. Formulations containing formoterol have been used, alone and in combination with inhaled corticosteroids, in the treatment of chronic obstructive pulmonary disease (COPD) and asthma.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Anderson, G.P. Formoterol: Pharmacology, molecular basis of agonism, and mechanism of long duration of a highly potent and selective β2-adrenoceptor agonist bronchodilator. Life Sci. 52(26), 2145-2160 (1993).

    2. Pacini, E.S.A., Sanders-Silveira, S., and Godinho, R.O. The extracellular cAMP-adenosine pathway in airway smooth muscle. J. Pharmacol. Exp. Ther. 366(1), 75-83 (2018).

    3. Sugiyama, H., Okada, C., Bewtra, A.K., et alThe effect of formoterol on the late asthmatic phenomena in guinea pigs. J. Allergy Clin. Immunol. 89(4), 858-866 (1992).

    4. Teng, L.S., Ying, Z.D., Sun, X.H., et alFormoterol, a clinically approved drug, inhibits ferroptosis by suppressing lipid peroxidation and attenuates APAP-induced acute liver injury. Chem. Biol. Interact. 421, 111724 (2025).