Abstract:
:Starting from the compound (3,4-dimethoxyphenyl)(2-(3,4-dimethoxyphenyl)cyclopent-1-en-1-yl)methanone (4), two diols and three tetrol derivatives were synthesised. Morover, from the reactions of 1,3-dimethoxybenzene and 1,4-dimethoxybenzene with adipoyl chloride, fifteen new along with nine known compounds were obtained. For the characterizations of compounds, spectroscopic methods such as NMR including DEPT, COSY, HMQC and HMBC experiments and X-ray diffraction were used. The antioxidant activities of novel synthesized seventeen molecules were investigated by analytical methods like ABTS•+ and DPPH• scavenging. Also, reducing power these molecules were investigated by Fe3+, Cu2+, and [Fe3+-(TPTZ)2]3+. Some of the molecules record powerful antioxidant profile when compared to putative standards. The inhibition effects of the phenols compounds against AChE and BChE activities were analysed. Also, these phenols were found as effective inhibitors for AChE, hCA I, hCA II, and BChE with Kis in the range of 122.95 ± 18.41-351.31 ± 69.12 nM for hCA I, 62.35 ± 9.03-363.17 ± 180.1 nM for hCA II, 134.57 ± 3.99-457.43 ± 220.10 nM for AChE, and 27.06 ± 9.12-72.98 ± 9.53 nM for BChE, respectively.
journal_name
Bioorg Chemjournal_title
Bioorganic chemistryauthors
Artunc T,Menzek A,Taslimi P,Gulcin I,Kazaz C,Sahin Edoi
10.1016/j.bioorg.2020.103884subject
Has Abstractpub_date
2020-07-01 00:00:00pages
103884eissn
0045-2068issn
1090-2120pii
S0045-2068(20)30292-3journal_volume
100pub_type
杂志文章abstract::Several novel N-substituted N-nitrosohydroxylamines were synthesized. They all inhibited mushroom tyrosinase, but the type of inhibition was different depending on the substituent. Some N-(mono- or dihydroxybenzyl)-N-nitrosohydroxylamines exhibited uncompetitive inhibition with respect to L-dopa. Among them, compound ...
journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/S0045-2068(03)00026-9
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2015.09.002
更新日期:2015-12-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2017.12.010
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2019.103329
更新日期:2019-12-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/0045-2068(92)90019-y
更新日期:1992-01-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
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更新日期:2019-10-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2018.12.013
更新日期:2019-04-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章,评审
doi:10.1016/j.bioorg.2013.11.004
更新日期:2014-02-01 00:00:00
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pub_type: 杂志文章
doi:10.1016/j.bioorg.2020.103690
更新日期:2020-04-01 00:00:00
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pub_type: 杂志文章
doi:10.1016/j.bioorg.2020.103981
更新日期:2020-08-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2018.08.012
更新日期:2018-12-01 00:00:00
abstract::The 3'-amino and carboxy functionalize thymidines execute their ribonucleolytic inhibition activity for angiogenin. These modified nucleosidic molecules inhibit the ribonucleolytic activity of angiogenin in a competitive manner like the other conventional nucleotidic inhibitors, which have been confirmed from kinetic ...
journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2013.11.005
更新日期:2014-02-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2020.104304
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更新日期:2019-08-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
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更新日期:2020-01-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
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更新日期:2020-09-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2006.11.006
更新日期:2007-04-01 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2019.03.067
更新日期:2019-07-01 00:00:00
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journal_title:Bioorganic chemistry
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更新日期:2019-07-01 00:00:00
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更新日期:2020-12-11 00:00:00
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journal_title:Bioorganic chemistry
pub_type: 杂志文章
doi:10.1016/j.bioorg.2020.104276
更新日期:2020-11-01 00:00:00
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