L-161982

CAS No. 147776-06-5

L-161982( —— )

Catalog No. M26732 CAS No. 147776-06-5

L-161982 is a selective antagonist of the EP4 receptor.

L-161982 is a selective antagonist of the EP4 receptor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 178 Get Quote
10MG 290 Get Quote
25MG 515 Get Quote
50MG 734 Get Quote
100MG 972 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    L-161982
  • Note
    Research use only, not for human use.
  • Brief Description
    L-161982 is a selective antagonist of the EP4 receptor.
  • Description
    L-161982 is a selective antagonist of the EP4 receptor.(In Vitro):In squamous carcinoma Tca8113 cells, L-161982 induces apoptosis and cell cycle arrest, and inhibits prostaglandin E2-induced proliferation . L-161982 (10 μM) blocks PGE2-stimulated cell proliferation of HCA-7 cells and ERK phosphorylation.(In Vivo):In collagen-induced arthritis (CIA) mice model, L-161982 (5 mg/kg; i.p.) reduces arthritis lesions and lesion progression. L-161982 shows less joint swelling and lower arthritis score after 35 days post immunization.
  • In Vitro
    L-161982 (10 μM; 2 hours) blocks PGE2-stimulated cell proliferation of HCA-7 cells.L-161982 (10 μM; 1 hour) blocks PGE2-stimulated ERK phosphorylation in HCA-7 cells.L-161982 induces apoptosis, cell cycle arrest, and inhibits prostaglandin E2-induced proliferation in oral squamous carcinoma Tca8113 cells. Cell Proliferation Assay Cell Line:HCA-7 cells Concentration:10 μM Incubation Time:2 hours Result:Blocked PGE2-induced cell proliferation.
  • In Vivo
    L-161982 (5?mg/kg; i.p.; once per day for 2 weeks) reduces arthritis lesions and lesion progression in CIA mice. Animal Model:Female DBA/1 mice of 6 to 8?weeks old (collagen-induced arthritis (CIA) mice model)Dosage:5?mg/kg Administration:i.p.; once per day for 2 weeks Result:Showed less joint swelling and lower arthritis score after 35?days post immunization.
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Prostaglandin Receptor
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    147776-06-5
  • Formula Weight
    654.72
  • Molecular Formula
    C32H29F3N4O4S2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (152.74 mM)
  • SMILES
    CCCCc1nn(-c2ccccc2C(F)(F)F)c(=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)c1sccc1C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Maljuri? N, et al. Quantitative structure -retention relationship modeling of selected antipsychotics and their impurities in green liquid chromatography using cyclodextrin mobile phases. Anal Bioanal Chem. 2018 Apr;410(10):2533-2550.
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