TY  - GEN 
AU  - Zoidis, G.
AU  - Loza García, María Isabel
AU  - Catto, M.
PY  - 2022
SN  - 1422-8599
UR  - http://hdl.handle.net/20.500.11940/20048
AB  - [EN] Based on previously highlighted structural features, the development of highly selective 5-HT1A receptor inhibitors is closely linked to the incorporation of a 4-alkyl-1-arylpiperazine scaffold on them. In this paper, we present the synthesis of...
LA  - en
TI  - Design, Synthesis and 5-HT1A Binding Affinity of N-(3-(4-(2-Methoxyphenyl)piperazin-1-yl)propyl)tricyclo[3.3.1.13,7 ]decan-1-amine and N-(3-(4-(2-Methoxyphenyl) piperazin-1-yl)propyl)-3,5-dimethyl-tricylo[3.3.1.13,7 ]decan-1-amine
DO  - 10.3390/M1353
KW  - AS Santiago
KW  - IDIS
VL  - 2022
ER  -