AJ-76

• Description:

  AJ-76 ((+) -AJ 76; (1S,2R) -AJ 76) is a dopamine autoreceptor antagonist. AJ-76 can increase the synthesis and turnover of dopamine in the rat brain, while having little effect on the synthesis and turnover of serotonin (5-HT) and norepinephrine. AJ-76 can also antagonize the sedative effects of low-dose apomorphine and has a weak antagonistic effect on postsynaptic dopamine receptor[1].

• Product Name Alternative:

  (+) -AJ 76; (1S,2R) -AJ 76

• UNSPSC:

  12352005

• Target:

  Dopamine Receptor

• Type:

  Reference compound

• Related Pathways:

  GPCR/G Protein; Neuronal Signaling

• Applications:

  Neuroscience-Neuromodulation

• Field of Research:

  Neurological Disease

• Assay Protocol:

  https://www.medchemexpress.com/aj-76.html

• Solubility:

  10 mM in DMSO

• Smiles:

  CCCN[C@H]1[C@@H](C)C2=C(C(OC)=CC=C2)CC1

• Molecular Formula:

  C15H23NO

• Molecular Weight:

  233.35

• References & Citations:

  [1]Svensson K, et al. (+) -AJ 76 and (+) -UH 232: central stimulants acting as preferential dopamine autoreceptor antagonists. Naunyn Schmiedebergs Arch Pharmacol. 1986 Nov;334 (3) :234-45.

• Shipping Conditions:

  Room temperature

• Scientific Category:

  Reference compound1

• Clinical Information:

  No Development Reported

• CAS Number:

  [85379-09-5]