JNJ-63533054

CAS No. 1802326-66-4

JNJ-63533054( JNJ 63533054 | JNJ63533054 | JNJ-63533054 )

Catalog No. M17383 CAS No. 1802326-66-4

JNJ-63533054 is a potent and selective agonist of hGPR139 with an EC50 = 16 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 65 In Stock
5MG 57 In Stock
10MG 85 In Stock
25MG 170 In Stock
50MG 268 In Stock
100MG 434 In Stock
200MG 622 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    JNJ-63533054
  • Note
    Research use only, not for human use.
  • Brief Description
    JNJ-63533054 is a potent and selective agonist of hGPR139 with an EC50 = 16 nM.
  • Description
    JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain and cell penetrant. JNJ 63533054 is selective for GPR139 over a panel of GPCRs, ion channels and transporters, including GPR142 and is orally bioavailable.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    JNJ 63533054 | JNJ63533054 | JNJ-63533054
  • Pathway
    Angiogenesis
  • Target
    Adrenergic Receptor
  • Recptor
    hGPR139
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    1802326-66-4
  • Formula Weight
    316.78
  • Molecular Formula
    C17H17ClN2O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 50 mg/mL 157.84 mM; H2O : < 0.1 mg/mL
  • SMILES
    C[C@@H](c1ccccc1)NC(=O)CNC(=O)c1cc(ccc1)Cl
  • Chemical Name
    3-Chloro-N-[2-oxo-2-[[(1S)-1-phenylethyl]amino]ethyl]benzamide

Shipping & Storage Information

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

Reference

1. Dvorak CA, et al. ACS Med Chem Lett. 2015 Jul 20;6(9):1015-8.
molnova catalog
related products
  • Phentolamine

    Phentolamine mesylate is an alpha-1 and alpha-2 selective adrenergic receptor antagonist.

  • Astragalus polypheno...

    Astragalus polyphenols is a compound isolated from the roots of Polygonum species, inhibits the formation of 5-HETE, HHT and thromboxane B2.

  • Flavone

    Flavons have effects on CYP (P450) activity which are enzymes that metabolize most drugs in the body.