208989-27-9Relevant articles and documents
Synthesis and monoamine transporter binding properties of 2,3-diaryltropanes
Kotturi, Sharadsrikar V.,Jiang, Songchun,Chang, An-Chih,Abraham, Philip,Navarro, Hernán A.,Kuhar, Michael J.,Carroll, F. Ivy
, p. 7437 - 7444 (2007/10/03)
Synthetic procedures were developed for the synthesis of 2β,3β- and 2α,3α-diaryltropanes. These compounds are analogues of the 3-aryltropane-2β-carboxylic acid methyl ester class of monoamine uptake inhibitors, where the 2β-carbomethoxy group has been rep
N-phenylalkyl-substituted tropane analogs of boat conformation with high selectivity for the dopamine versus serotonin transporter
Prakash,Tamiz, Amir P.,Araldi, Gian Luca,Zhang, Mei,Johnson, Kenneth M.,Kozikowski, Alan P.
, p. 3325 - 3328 (2007/10/03)
A series of N-phenylalkyl-substituted tropane analogs of boat conformation was synthesized, and these tropanes were evaluated for their ability to inhibit high affinity uptake of dopamine (DA) and serotonin (5HT) into striatal nerve endings (synaptosomes). Some of these compounds exhibit high affinity for the DA transporter with a 5-HT/DA transporter selectivity ratio of >50.
Synthesis and biological properties of new 2β-alkyl- and 2β-aryl-3- (substituted phenyl)tropane derivatives: Stereochemical effect of C-3 on affinity and selectivity for neuronal dopamine and serotonin transporters
Kozikowski, Alan P.,Araldi, Gian Luca,Prakash,Zhang, Mei,Johnson, Kenneth M.
, p. 4973 - 4982 (2007/10/03)
In our efforts to identify molecules that might act as cocaine antagonists or cocaine partial agonists, we have been involved in efforts to further elucidate the nature of cocaine's binding to the dopamine transporter (DAT) through strategic modifications