Chellappan_2006_J.Med.Chem_49_2673

Reference

Title : Synthesis and pharmacological evaluation of novel 9- and 10-substituted cytisine derivatives. Nicotinic ligands of enhanced subtype selectivity - Chellappan_2006_J.Med.Chem_49_2673
Author(s) : Chellappan SK , Xiao Y , Tueckmantel W , Kellar KJ , Kozikowski AP
Ref : Journal of Medicinal Chemistry , 49 :2673 , 2006
Abstract :

We report the synthesis and pharmacological properties of several cytisine derivatives. Among them, two 10-substituted derivatives showed much higher selectivities for the alpha4beta2 nAChR subtype in binding assays than cytisine. The 9-vinyl derivative was found to have a very similar agonist activity profile to that of cytisine.

PubMedSearch : Chellappan_2006_J.Med.Chem_49_2673
PubMedID: 16640326

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Citations formats

Chellappan SK, Xiao Y, Tueckmantel W, Kellar KJ, Kozikowski AP (2006)
Synthesis and pharmacological evaluation of novel 9- and 10-substituted cytisine derivatives. Nicotinic ligands of enhanced subtype selectivity
Journal of Medicinal Chemistry 49 :2673

Chellappan SK, Xiao Y, Tueckmantel W, Kellar KJ, Kozikowski AP (2006)
Journal of Medicinal Chemistry 49 :2673