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@ARTICLE{Glykofridi:256473,
author = {Glykofridi, Pigi and Tziouri, Vassiliki-Eleni and
Xanthopoulos, Konstantinos and Vlachou, Maria-Eirini and
Silva-Correia, Susana and Fischer, Anna-Lisa and Thüne,
Katrin and Hatzidimitriou, Antonios and Zerr, Inga and
Schmitz, Matthias and Sklaviadis, Theodoros and
Hadjipavlou-Litina, Dimitra and Papagiannopoulou, Dionysia},
title = {{S}ynthesis, structural characterization and study of
antioxidant and anti-{P}r{PS}c properties of flavonoids and
their rhenium({I})-tricarbonyl complexes.},
journal = {Journal of biological inorganic chemistry},
volume = {28},
number = {2},
issn = {0949-8257},
address = {New York},
publisher = {Springer},
reportid = {DZNE-2023-00335},
pages = {235 - 247},
year = {2023},
note = {CC BY},
abstract = {This study aims at the synthesis and initial biological
evaluation of novel rhenium-tricarbonyl complexes of
3,3',4',5,7-pentahydroxyflavone (quercetin),
3,7,4΄-trihydroxyflavone (resokaempferol),
5,7-dihydroxyflavone (chrysin) and
4΄,5,7-trihydroxyflavonone (naringenin) as neuroprotective
and anti-PrP agents. Resokaempferol was synthesized from
2,2΄,4-trihydroxychalcone by H2O2/NaOH. The
rhenium-tricarbonyl complexes of the type
fac-[Re(CO)3(Fl)(sol)] were synthesized by reacting the
precursor fac-[Re(CO)3(sol)3]+ with an equimolar amount of
the flavonoids (Fl) quercetin, resokaempferol, chrysin and
naringenin and the solvent (sol) was methanol or water. The
respective Re-flavonoid complexes were purified by
semi-preparative HPLC and characterized by spectroscopic
methods. Furthermore, the structure of Re-chrysin was
elucidated by X-ray crystallography. Initial screening of
the neuroprotective properties of these compounds included
the in vitro assessment of the antioxidant properties by the
DPPH assay as well as the anti-lipid peroxidation of
linoleic acid in the presence of AAPH and their ability to
inhibit soybean lipoxygenase. From the above studies, it was
concluded that the complexes' properties are mainly
correlated with the structural characteristics and the
presence of the flavonoids. The flavonoids and their
respective Re-complexes were also tested in vitro for their
ability to inhibit the formation and aggregation of the
amyloid-like abnormal prion protein, PrPSc, by employing the
real-time quaking-induced conversion assay with recombinant
PrP seeded with cerebrospinal fluid from patients with
Creutzfeldt-Jakob disease. All the compounds blocked de novo
abnormal PrP formation and aggregation.},
keywords = {Flavonoids: chemistry / Humans / Antioxidants: pharmacology
/ Rhenium: chemistry / Quercetin / Hydrogen Peroxide /
Crystallography, X-Ray / Flavonoids: pharmacology / PrPSc
Proteins: drug effects / PrPSc Proteins: metabolism /
Organometallic Compounds: chemistry / Organometallic
Compounds: pharmacology / Flavonoids (NLM Chemicals) /
Anti-oxidant (Other) / Flavonoids (Other) / Lipid
peroxidation (Other) / Lipoxygenase (Other) / Prion diseases
(Other) / Rhenium complexes (Other) / Antioxidants (NLM
Chemicals) / Rhenium (NLM Chemicals) / Quercetin (NLM
Chemicals) / Hydrogen Peroxide (NLM Chemicals) /
5-deoxykaempferol (NLM Chemicals) / chrysin (NLM Chemicals)
/ naringenin (NLM Chemicals) / PrPSc Proteins (NLM
Chemicals) / Organometallic Compounds (NLM Chemicals)},
cin = {AG Zerr / Ext UMG Zerr / AG Fischer},
cid = {I:(DE-2719)1440011-1 / I:(DE-2719)5000037 /
I:(DE-2719)1410002},
pnm = {353 - Clinical and Health Care Research (POF4-353) / 352 -
Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-353 / G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36695886},
pmc = {pmc:PMC9981504},
doi = {10.1007/s00775-022-01986-9},
url = {https://pub.dzne.de/record/256473},
}