Therapeutic targeting of α7 nicotinic acetylcholine receptors

RL Papke, NA Horenstein, H Khoshbouei - Pharmacological Reviews, 2021 - Elsevier
The α7-type nicotinic acetylcholine receptor is one of the most unique and interesting of all
the members of the cys-loop superfamily of ligand-gated ion channels. Since it was first …

5-Amino-pyrazoles: potent reagents in organic and medicinal synthesis

A Shaabani, MT Nazeri, R Afshari - Molecular diversity, 2019 - Springer
Amino-pyrazoles have proven to be a class of fascinating and privileged organic tools for the
construction of diverse heterocyclic or fused heterocyclic scaffolds. This review presents …

Novel therapeutic strategies for dementia

R Cacabelos, C Torrellas, I Carrera… - CNS & Neurological …, 2016 - ingentaconnect.com
Dementia represents a major problem of health and disability, with a relevant economic
impact on our society. Despite important advances in pathogenesis, diagnosis and …

Synthesis and biological activities of indolizine derivatives as alpha-7 nAChR agonists

Y Xue, J Tang, X Ma, Q Li, B Xie, Y Hao, H Jin… - European Journal of …, 2016 - Elsevier
Human α7 nicotinic acetylcholine receptor (nAChR) is a promising therapeutic target for the
treatment of schizophrenia accompanied with cognitive impairment. Herein, we report the …

3-((Hetera) cyclobutyl) azetidines,“stretched” analogues of piperidine, piperazine, and morpholine: Advanced building blocks for drug discovery

IO Feskov, AV Chernykh, YO Kuchkovska… - The Journal of …, 2018 - ACS Publications
Four 3-((hetera) cyclobutyl) azetidine-based isosteres of piperidine, piperazine, and
morpholine were designed and synthesized on up to gram scale. The key step of the …

Syntheses, spectroscopic investigation and electronic properties of two sulfonamide derivatives: a combined experimental and quantum chemical approach

A Mahmood, T Akram, EB de Lima - Journal of Molecular Structure, 2016 - Elsevier
Two sulfonamides derivatives, N-phenethyl-4-methylbenzenesulfonamide (1) and N-(4-
hydroxyphenethyl)-4-methylbenzenesulfonamide (2), were successfully synthesized and …

Novel N-(Heterocyclylphenyl)benzensulfonamide Sharing an Unreported Binding Site with T-Cell Factor 4 at the β-Catenin Armadillo Repeats Domain as an …

M Nalli, L Di Magno, Y Wen, X Liu… - ACS Pharmacology & …, 2023 - ACS Publications
Despite intensive efforts, no inhibitors of the Wnt/β-catenin signaling pathway have been
approved so far for the clinical treatment of cancer. We synthesized novel N …

Design of α7 nicotinic acetylcholine receptor ligands using the (het) Aryl-1, 2, 3-triazole core: Synthesis, in vitro evaluation and SAR studies

A Ouach, F Pin, E Bertrand, J Vercouillie… - European Journal of …, 2016 - Elsevier
We report here the synthesis of a large library of 1, 2, 3-triazole derivatives which were in
vitro tested as α7 nAchR ligands. The SAR study revealed that several crucial factors are …

Design and synthesis of N-(1-(6-(substituted phenyl)-pyridazin-3-yl)-piperidine-3-yl)-amine derivatives as JMJD6 inhibitors

Y Qian, M Ao, B Li, Z Kuang, X Wang, Y Cao, J Li… - Bioorganic …, 2022 - Elsevier
JMJD6 is a member of the JmjC domain-containing family and has been identified as a
promising therapeutic target for treating estrogen-induced and triple-negative breast cancer …

The recent development of α7 nicotinic acetylcholine receptor (nAChR) ligands as therapeutic candidates for the treatment of central nervous system (CNS) diseases

C Beinat, S D. Banister, M Herrera… - Current Pharmaceutical …, 2016 - benthamdirect.com
Homomeric α7 nicotinic acetylcholine receptors (nAChRs) are implicated in the regulation of
cognitive processes such as memory and attention and have potential as therapeutic targets …