Results 51 to 60 of about 605 (157)

Structure-retention relationship study of arylpiperazines by linear multivariate modeling

open access: yes, 2010
A quantitative structure retention relationship study has been performed to correlate the retention of 33 newly synthesized arylpiperazines with their molecular characteristics, using thin-layer chromatography.
Andrić, Filip   +11 more
core   +1 more source

Discovery of Bishomo(hetero)arylpiperazines as Novel Multifunctional Ligands Targeting Dopamine D3 and Serotonin 5-HT1A and 5-HT2A Receptors

open access: yes, 2016
As a continuation of our efforts to develop innovative ligands for D3, 5-HT1A, and 5-HT2A receptors with low propensity to block hERG channels, we propose a series bishetero(homo)arylpiperazines 5a−m as novel and potent multifunctional ligands ...
Karin Sandager-Nielsen (1714315)   +16 more
core   +1 more source

Ionization constants and partition coefficients of 1-arylpiperazine derivatives

open access: yesJournal of Pharmacy and Pharmacology, 1985
AbstractThe ionization constant (pKa and liposolubilities (log P) of fourteen 1-arylpiperazines were determined by n-octanol/buffer partition. pKa varied little across the entire series. Log P values ranged from less than 1 to about 2 for the highly lipophilic derivatives of the preset series.
S, Caccia, M H, Fong, R, Urso
openaire   +2 more sources

5-HT1A- versus D2-Receptor Selectivity of Flesinoxan and Analogous N4-Substituted N1-Arylpiperazines

open access: yes, 2016
We investigated the structural requirements for high 5-HT1A affinity of the agonist flesinoxan and its selectivity versus D2 receptors. For this purpose a series of arylpiperazine congeners of flesinoxan were synthesized and evaluated for their ability ...
Martin Th. M. Tulp (2665003)   +7 more
core   +1 more source

Synthesis and pharmacological evaluation of N-{4-[2-(4-arylpiperazin-1- yl)ethyl]phenyl} arylamides [PDF]

open access: yes, 2019
Serotonin 5HT1a receptor belongs to a class of G-protein coupled receptors. It serves as a potential target for neurological disorders such as depression, anxiety etc.
Dukic-Stefanovic, Sladjana   +5 more
core   +3 more sources

Mixed dopaminergic/serotonergic properties of several 2-substituted 4-[2-(5-benzimidazole)ethyl]-1-arylpiperazines

open access: yes, 1998
A series of substituted 4-[2-(5-benzimidazole)ethyl]-arylpiperazines was synthesized by introducing different substituents into position 2 of benzimidazole ring of 4-[2-(N,N-di-n-propylamino)ethyl]-1,2-diaminobenzenes.
Kostić Rajačić, Slađana   +2 more
core   +1 more source

Poster Sessions

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Discovery and Preliminary Structure–Activity Relationship of Arylpiperazines as Novel, Brain-Penetrant Antiprion Compounds

open access: yes, 2016
Creutzfeldt-Jakob disease and kuru in humans, BSE in cattle, and scrapie in sheep are fatal neurodegenerative disorders. Such illnesses are caused by the conversion and accumulation of a misfolded pathogenic isoform (termed PrPSc) of a normally benign ...
Stanley B. Prusiner (190817)   +5 more
core   +1 more source

Binding of Arylpiperazines, (Aryloxy)propanolamines, and Tetrahydropyridylindoles to the 5-HT1A Receptor:  Contribution of the Molecular Lipophilicity Potential to Three-Dimensional Quantitative Structure−Affinity Relationship Models

open access: yes, 2016
A set of 280 5-HT1A receptor ligands were selected from available literature data according to predefined criteria and subjected to three-dimensional quantitative structure−affinity relationship analysis using comparative molecular field analysis.
Pierre-Alain Carrupt (522894)   +3 more
core   +1 more source

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