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Chemical Compound Review

Lopac-D-132     3-[2-(dipropylamino)ethyl]- 1H-indole-5...

Synonyms: Dipropyl-5-CT, SureCN8891095, DP-5-CT, DP5CT, CCG-204501, ...
 
 
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High impact information on DP-5-CT

  • Concentration-response curves were generated for inhibition of forskolin-stimulated adenylyl cyclase activity by 5-HT and the selective 5-HT1A agonist N,N-dipropyl-5-carboxamidotryptamine (DP-5-CT) [1].
  • Adenylyl cyclase activity in CHO-K1 cells transiently transfected with GP2-7 was stimulated by several analogues of 5-HT with the following order of potency: 5-CT > 5-HT = 5-MeOT > dipropyl-5-CT > 8-OH-DPAT [2].
  • 4. Dipropyl-5-CT selectively depressed MSR and CON SLOW (IC50 90-170 nM) but was less potent than 5-CT [3].
 

Anatomical context of DP-5-CT

 

Analytical, diagnostic and therapeutic context of DP-5-CT

References

 
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