AP1189 acetate

CAS No. 959850-74-9

AP1189 acetate( —— )

Catalog No. M28790 CAS No. 959850-74-9

AP1189 acetate is a biased agonist at melanocortin 1 and melanocortin 3 receptors.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 104 In Stock
5MG 79 In Stock
10MG 129 In Stock
25MG 235 In Stock
50MG 342 In Stock
100MG 486 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    AP1189 acetate
  • Note
    Research use only, not for human use.
  • Brief Description
    AP1189 acetate is a biased agonist at melanocortin 1 and melanocortin 3 receptors.
  • Description
    AP1189 acetate is a biased agonist at melanocortin 1 and melanocortin 3 receptors.(In Vitro):Added to macrophage cultures, AP1189 reduced cytokine release, an effect reliant on both MC1 and MC3 as evident from the use of Mc1r(-/-) and Mc3r(-/-) macrophages. No melanogenesis was induced by AP1189 in B16-F10 melanocytes.(In Vivo):Oral AP1189 elicited anti-inflammatory actions in peritonitis and, upon administration at the peak of inflammation, accelerated the resolution phase by ~3-fold.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Melanocortin Receptor
  • Recptor
    calmodulin
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    959850-74-9
  • Formula Weight
    358.35
  • Molecular Formula
    C16H18N6O4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=[N+](C1=CC=CC=C1N2C(/C=C/C=N/NC(N)=N)=CC=C2)[O-].CC(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Noriko Koizumi, et al. Combined agent for cell therapy of corneal endothelial cell. US10959997B2
molnova catalog
related products
  • MSG 606

    Potent human MC1 receptor antagonist (IC50 = 17 nM). Also partial agonist at human MC3 and MC5 receptors (EC50 values are 59 and 1300 nM, respectively). Exhibits binding affinity for A375 melanoma cells in vitro. Reverses morphine-induced hyperalgesia in female mice, with no effect in male mice. γMSH analog.

  • [D-Trp8]-γ-MSH

    Selective melanocortin 3 (MC3) receptor agonist (IC50 values are 6.7, 340 and 600 nM for human MC3, MC5 and MC4 receptors respectively). Displays anti-inflammatory efficacy.

  • Setmelanotide Acetat...

    Setmelanotide Acetate(920014-72-8 free base) (RM-493 Acetate) is a selective agonist of melanocortin 4 receptor (MC4R)(human and rat MC4R with EC50s of 0.27 nM and 0.28 nM, respectively).