Small molecules selectively targeting sigma-1 receptor for the treatment of neurological diseases

N Ye, W Qin, S Tian, Q Xu, EA Wold… - Journal of medicinal …, 2020 - ACS Publications
The sigma-1 (σ1) receptor, an enigmatic protein originally classified as an opioid receptor
subtype, is now understood to possess unique structural and functional features of its own …

Discovery of novel quinazoline-2-aminothiazole hybrids containing a 4-piperidinylamide linker as potential fungicides against the phytopathogenic fungus Rhizoctonia …

M Ding, N Wu, Q Lin, Y Yan, Y Yang… - Journal of Agricultural …, 2022 - ACS Publications
A total of 29 novel quinazoline-2-aminothiazole hybrids containing a 4-piperidinylamide
linker were designed, synthesized, and evaluated for their anti-microbial properties against …

[HTML][HTML] Sigma-1 receptor as a potential pharmacological target for the treatment of neuropathology

AV Bolshakova, EO Kukanova, AN Gainullina… - … Journal: Physics and …, 2016 - Elsevier
Sigma receptors are usually classified as a separate class of intracellular receptors. Among
them the sigma-1 receptor has been the most studied regarding its pharmacological …

Neuroprotection in non-transgenic and transgenic mouse models of Alzheimer's disease by positive modulation of σ1 receptors

T Maurice, JN Volle, M Strehaiano, L Crouzier… - Pharmacological …, 2019 - Elsevier
Abstract The sigma-1 (σ 1) receptor is an endoplasmic reticulum (ER) chaperone protein,
enriched in mitochondria-associated membranes. Its activation triggers physiological …

Aryl sulfonium salt electron donor-acceptor complexes for halogen atom transfer: Isocyanides as tunable coupling partners

H Zhao, VD Cuomo, JA Rossi-Ashton, DJ Procter - Chem, 2024 - cell.com
The photoactivation of sulfonium salt EDA (electron donor-acceptor) complexes provides a
mild platform for aryl-radical-mediated halogen atom transfer activation of a wide range of …

Synthesis, cytotoxicity and antiviral evaluation of new series of imidazo [4, 5-g] quinoline and pyrido [2, 3-g] quinoxalinone derivatives

I Briguglio, R Loddo, E Laurini, M Fermeglia… - European Journal of …, 2015 - Elsevier
Linear aromatic N-tricyclic compounds with promising antiviral activity and minimal
cytotoxicity were prepared and analyzed in the last years. Specifically, the pyrido [2, 3-g] …

Design, Synthesis, Antifungal Activity, and Mechanism of Action of New Piperidine-4-carbohydrazide Derivatives Bearing a Quinazolinyl Moiety

Y Yang, S Liu, T Yan, M Yi, H Li… - Journal of Agricultural and …, 2024 - ACS Publications
A series of new piperidine-4-carbohydrazide derivatives bearing a quinazolinyl moiety were
prepared and evaluated for their fungicidal activities against agriculturally important fungi …

Discovery of novel indolylarylsulfones as potent HIV-1 NNRTIs via structure-guided scaffold morphing

T Zhao, Q Meng, D Kang, J Ji, E De Clercq… - European Journal of …, 2019 - Elsevier
For more in-depth exploration of the chemical space around the entrance channel of HIV-1
reverse transcriptase (RT), a series of novel indolylarylsulfones (IASs) bearing different …

New neurogenic lipoic-based hybrids as innovative Alzheimer's drugs with σ-1 agonism and β-secretase inhibition

M Estrada, C Pérez, E Soriano, E Laurini… - Future Medicinal …, 2016 - Taylor & Francis
Background: Neurogenic agents emerge as innovative drugs for the treatment of Alzheimer's
disease (AD), whose pathological complexity suggests strengthening research in the multi …

Synthesis and Structure–Affinity Relationships of Spirocyclic Benzopyrans with Exocyclic Amino Moiety

E Kronenberg, F Weber, S Brune… - Journal of Medicinal …, 2019 - ACS Publications
σ1 and/or σ2 receptors play a crucial role in pathological conditions such as pain,
neurodegenerative disorders, and cancer. A set of spirocyclic cyclohexanes with diverse O …