| Literature DB >> 29576509 |
Hua Cheng1, Wei Song1, Ren Nie1, Yu-Xia Wang2, Hui-Lian Li1, Xiang-Sheng Jiang1, Jun-Jun Wu1, Cheng Chen3, Qiong-You Wu4.
Abstract
Succinate-cytochrome c reductase (SCR) is composed of a mixture of mitochondrial complex II (succinate-ubiquinone oxidoreductase) and complex III (cytochrome bc1 complex). Meanwhile, complexes II and III are two promising targets of numerous antibiotics and fungicides. With an aim to identify new lead structures for SCR, complex II or III, a new series of 4-aryloxy-N-arylanilines were synthesized by introducing a 4-aryloxy phenyl group as one of the aryl groups in diaryl amines. With the economic Cu(OAc)2·H2O as the optimal copper promoter, a simple and facile protocol was utilized to afford 24 target products in 56-93% yields. Furthermore, extensive screening results suggested variable inhibitory activities of these compounds against SCR. Exceptionally, compounds 7k-7n showed excellent inhibition potency with their IC50 values in the nanomolar range, demonstrating higher potency than the commercial controls (penthiopyrad and azoxystrobin) by over one order of magnitude.Entities:
Keywords: 4-Aryloxy-N-arylanilines; Inhibitory activities; Mitochondrial complex II; Mitochondrial complex III; Succinate-cytochrome c reductase (SCR); Synthesis
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Year: 2018 PMID: 29576509 DOI: 10.1016/j.bmcl.2018.03.014
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823