Design, synthesis and comparison of water-soluble phthalocyanine/porphyrin analogues and their inhibition effects on Aβ42 fibrillization. Issue 14 (18th June 2021)

• Record Type: Journal Article
• Authors: Xu, Weiyuan; Gao, Chao; Sun, Xinyang; Tai, William Chi-Shing; Lung, Hong Lok; Law, Ga-Lai
• Is Part Of: Inorganic chemistry frontiers. Volume 8:Issue 14(2021)
• Page Start: 3501
• Page End: 3513
• Publication Date: 2021-06-18
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d1qi00237f
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : A series of ZnPorp and ZnPc conjugates were synthesized and compared by their inhibitory effects on Aβ42 fibrillization. We show that ZnPc conjugates designed with a good hydrophilic–hydrophobic balance are deemed as better inhibitors. Abstract : The misfolding and fibrillization of β amyloid (Aβ) is a major pathological hallmark of Alzheimer's disease (AD) and creates an important niche for developing targeted probe and drug designs. Phthalocyanine and porphyrin analogues are known to interact with Aβ species and interrupt their aggregation, and in this study we show that by conjugating with small molecules that can function as Aβ aggregation blockers such as curcumin and bexarotene, drug candidates with improved potential can be developed. In this work, we investigated porphyrin zinc (ZnPorp) analogues and phthalocyanine zinc (ZnPc) conjugates and compared their inhibitory effects on the formation of Aβ42 fibrils. We show that probe designs with a good hydrophilic–hydrophobic balance as observed with the ZnPc conjugate analogues are deemed as better inhibitors in modulating Aβ42 aggregation.