Virtual Screening and Structure-Based Discovery of Indole Acylguanidines as Potent β-secretase (BACE1) Inhibitors
Proteolytic cleavage of amyloid precursor protein by β-secretase (BACE1) is a key step in generating the N-terminal of β-amyloid (Aβ), which further forms into amyloid plaques that are considered as the hallmark of Alzheimer’s disease. Inhibitors of BACE1 can reduce the levels of Aβ and thus have a...
Main Authors: | Bing Xiong, Yechun Xu, Jingkang Shen, Xin Wang, Lanping Ma, Tiantian Chen, Wuyan Chen, Yiquan Zou, Li Li |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2013-05-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/18/5/5706 |
Similar Items
-
Targeting the Oncoprotein Smoothened by Small Molecules: Focus on Novel Acylguanidine Derivatives as Potent Smoothened Inhibitors
by: Silvia Pietrobono, et al.
Published: (2018-12-01) -
Theoretical investigation and design of some indole derivatives as potent β-glucuronidase inhibitors
by: Muhammad Tukur Ibrahim, et al.
Published: (2020-07-01) -
Discovery of indole-3-butyric acid derivatives as potent histone deacetylase inhibitors
by: Yiming Chen, et al.
Published: (2021-01-01) -
Identification of Novel and Potent Indole-Based Benzenesulfonamides as Selective Human Carbonic Anhydrase II Inhibitors: Design, Synthesis, In Vitro, and In Silico Studies
by: Ahmed Elkamhawy, et al.
Published: (2022-02-01) -
2-[(2-Fluorophenyl)(1H-indol-3-yl)methyl]-1H-indole
by: R. Anil Kumar, et al.
Published: (2016-06-01)