ML-184

CAS No. 794572-10-4

ML-184( CID2440433 )

Catalog No. M22218 CAS No. 794572-10-4

ML-184 is a potent synthetic agonist of GPR55 with EC50 of 0.26 μM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 80 In Stock
5MG 77 In Stock
10MG 132 In Stock
25MG 242 In Stock
50MG 356 In Stock
100MG 538 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ML-184
  • Note
    Research use only, not for human use.
  • Brief Description
    ML-184 is a potent synthetic agonist of GPR55 with EC50 of 0.26 μM.
  • Description
    ML-184 is a potent synthetic agonist of GPR55 with EC50 of 0.26 μM.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    CID2440433
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    GPR55
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    794572-10-4
  • Formula Weight
    470.63
  • Molecular Formula
    C25H34N4O3S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 12.5 mg/mL (26.56 mM)
  • SMILES
    O=S(C1=CC=C(N2CCCC2)C(C(N3CCN(C4=CC=CC(C)=C4C)CC3)=O)=C1)(N(C)C)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Celorrio M , Rojo-Bustamante, Estefanía, Fernández-Suárez, Diana, et al. GPR55: A therapeutic target for Parkinson's disease?[J]. Neuropharmacology, 2017, 125:319-332.
molnova catalog
related products
  • CTOP

    Potent and selective μ opioid receptor antagonist (Ki values are 0.96 and >10,000 nM for μ and δ receptors respectively). Causes behavioral effects on central administration in vivo. Also increases K+ currents in rat locus ceruleus neurons in vitro via a μ receptor independent mechanism.

  • Nalfurafine hydrochl...

    Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1,200 nM, respectively).

  • [Nphe1]Nociceptin(1-...

    Selective and competitive nociceptin receptor antagonist, devoid of any agonist activity. Binds selectively to recombinant nociceptin receptors (pKi = 8.4), and competitively antagonizes the actions of nociceptin in vitro and in vivo.