ABT 724 trihydrochloride

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Names

[ CAS No. ]:
587870-77-7

[ Name ]:
ABT 724 trihydrochloride

[Synonym ]:
MFCD08703101
1H-Benzimidazole, 2-[[4-(2-pyridinyl)-1-piperazinyl]methyl]-, hydrochloride (1:3)
2-{[4-(2-Pyridinyl)-1-piperazinyl]methyl}-1H-benzimidazole trihydrochloride
2-{[4-(Pyridin-2-yl)piperazin-1-yl]methyl}-1H-benzimidazole trihydrochloride
ABT-724 trihydrochloride

Chemical & Physical Properties

[ Molecular Formula ]:
C17H22Cl3N5

[ Molecular Weight ]:
402.749

[ Exact Mass ]:
401.094086

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ RIDADR ]:
NONH for all modes of transport

Articles

Effects of selective dopaminergic compounds on a delay-discounting task.

Behav. Pharmacol. 22 , 300-11, (2011)

Impulsivity is widely regarded as a multidimensional trait that encompasses two or more distinct patterns of behavior, and dopaminergic systems are implicated in the expression of impulsive behavior i...

Dopamine D4 receptor involvement in the discriminative stimulus effects in rats of LSD, but not the phenethylamine hallucinogen DOI.

Psychopharmacology 203 , 265-77, (2009)

Lysergic acid diethylamide (LSD) differs from other types of hallucinogens in that it possesses direct dopaminergic effects. The exact nature of this component has not been elucidated.The present stud...

Penile erection and yawning induced by dopamine D2-like receptor agonists in rats: influence of strain and contribution of dopamine D2, but not D3 and D4 receptors.

Behav. Pharmacol. 20 , 303-11, (2009)

Dopamine (DA) is implicated in penile erection (PE) and yawning (YA) in rats through activation of D2-like receptors. However, the exact role of each subtype (D2, D3 and D4) of this receptor family in...


More Articles


Related Compounds

  • abt 724 trihydrochloride
  • ABT 724 trihydrochloride
  • ABT-724
  • ABT 639
  • ABT-089
  • 2-(4-(2-((2S,5R)-2-cyano-5-ethynylpyrrolidin-1-yl)-2-oxoethylamino)-4-methylpiperidin-1-yl)isonicotinic acid L-malate
  • 2-(Bromomethyl)-3,3-dimethyl-2-(2-methylpropoxy)bicyclo[2.2.1]heptane
  • tert-butyl N-ethyl-N-[3-iodo-2-methyl-2-(2-methylpropoxy)propyl]carbamate
  • 1-[1-Bromo-2-(2-methylpropoxy)propan-2-yl]-2-fluorobenzene
  • Tert-butyl 3-(iodomethyl)-3-(2-methylpropoxy)piperidine-1-carboxylate
  • 1-Bromo-2-[2-iodo-1-(2-methylpropoxy)ethyl]benzene
  • 1-Bromo-2-[1-bromo-2-(2-methylpropoxy)propan-2-yl]benzene
  • 3-Iodo-4-(2-methylpropoxy)-1lambda6-thiolane-1,1-dione
  • 1-{[(3-Bromo-1,4-dichlorobutan-2-yl)oxy]methyl}-2-chlorobenzene
  • tert-butyl N-[3-bromo-2-methyl-2-(3-methylbutoxy)propyl]-N-ethylcarbamate
  • 4-(Bromomethyl)-4-(3-methylbutoxy)oxane
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