A non-prostaglandin EP2 receptor agonist
Related Products
Technical Support & Resources

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.

Omidenepag (free acid)

Item No. 41045

Technical Information
Formal Name
N-[6-[[[[4-(1H-pyrazol-1-yl)phenyl]methyl](3-pyridinylsulfonyl)amino]methyl]-2-pyridinyl]-glycine
CAS Number
1187451-41-7
Synonyms
  • UR-7276
Molecular Formula
C23H22N6O4S
Formula Weight
Purity
≥98%
Formulation
A solid
Acetonitrile: Slightly soluble: 0.1-1 mg/mlDMSO: Sparingly soluble: 1-10 mg/ml
SMILES
O=[S](N(CC1=CC=C(N2C=CC=N2)C=C1)CC3=CC=CC(NCC(O)=O)=N3)(C4=CN=CC=C4)=O
InChi Code
InChI=1S/C23H22N6O4S/c30-23(31)15-25-22-6-1-4-19(27-22)17-28(34(32,33)21-5-2-11-24-14-21)16-18-7-9-20(10-8-18)29-13-3-12-26-29/h1-14H,15-17H2,(H,25,27)(H,30,31)
InChi Key
YHGSTSNEOJUIRN-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice 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

    Omidenepag is a non-prostaglandin agonist of the prostaglandin E2 (PGE2) receptor subtype EP2 and an active metabolite of the prodrug omidenepag isopropyl ester.1 It selectively binds to human EP2 over EP1, EP3, and EP4 receptors (IC50s = 10, >10,000, >10,000, and 5,480 nM, respectively) and induces cAMP accumulation in HEK293 cells expressing human EP2 receptors (EC50 = 1.1 nM).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Iwamura, R., Tanaka, M., Okanari, E., et alIdentification of a selective, non-prostanoid EP2 receptor agonist for the treatment of glaucoma: Omidenepag and its prodrug omidenepag isopropyl. J. Med. Chem. 61(15), 6869-6891 (2018).