Unknown

Dataset Information

0

Microtiter plate-based chemistry and in situ screening: SuFEx-enabled lead discovery of selective AChE inhibitors.


ABSTRACT: Sulphur fluoride exchange (SuFEx) is a category of click chemistry that enables covalent linking of modular units through sulphur connective hubs. Here, we reported an efficient synthesis and in situ screening method for building a library of sulphonamides on the picomolar scale by SuFEx reaction between a sulphonyl fluoride (RSO2F) core and primary or secondary amines. This biocompatible SuFEx reaction would allow us to rapidly synthesise sulphonamide molecules, and evaluate their ChE inhibitory activity. Compound T14-A24 was identified as a reversible, competitive, and selective AChE inhibitor (Ki = 22 nM). The drug-like evaluation showed that T14-A24 had benign BBB penetration, remarkable neuroprotective effect, and safe toxicological profile. In vivo behavioural study showed that T14-A24 treatment improved the Aβ1 - 42-induced cognitive impairment, significantly prevented the effects of Aβ1 - 42 toxicity. Therefore, this SuFEx click reaction can accelerate the discovery of lead compounds.

SUBMITTER: Tang K 

PROVIDER: S-EPMC10388794 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Microtiter plate-based chemistry and in situ screening: SuFEx-enabled lead discovery of selective AChE inhibitors.

Tang Kun K   Li Huan-Huan HH   Wu Chengyao C   Zhang Shi-Long SL   Yang Jian-Guo JG   Tang Wenjian W   Qin Hua-Li HL  

Journal of enzyme inhibition and medicinal chemistry 20231201 1


Sulphur fluoride exchange (SuFEx) is a category of click chemistry that enables covalent linking of modular units through sulphur connective hubs. Here, we reported an efficient synthesis and <i>in situ</i> screening method for building a library of sulphonamides on the picomolar scale by SuFEx reaction between a sulphonyl fluoride (RSO<sub>2</sub>F) core and primary or secondary amines. This biocompatible SuFEx reaction would allow us to rapidly synthesise sulphonamide molecules, and evaluate t  ...[more]

Similar Datasets

| S-EPMC6192542 | biostudies-literature
| S-EPMC7751259 | biostudies-literature
| S-EPMC6754619 | biostudies-literature
| S-EPMC11145270 | biostudies-literature
| S-EPMC8867595 | biostudies-literature
| S-EPMC2866662 | biostudies-literature
| S-EPMC9881234 | biostudies-literature
| S-EPMC8864708 | biostudies-literature
| S-EPMC10935723 | biostudies-literature
| S-EPMC9090990 | biostudies-literature