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- Publications
- Influence
Structural and thermodynamical properties of CuII amyloid-β16/28 complexes associated with Alzheimer’s disease
- Luc Guilloreau, L. Damian, Y. Coppel, H. Mazarguil, M. Winterhalter, P. Faller
- Chemistry, Medicine
- JBIC Journal of Biological Inorganic Chemistry
- 22 August 2006
The aggregation of the peptide amyloid-β (Aβ) to form amyloid plaques is a key event in Alzheimer’s disease. It has been shown that CuII can bind to soluble Aβ and influence its aggregation… Expand
Amyloid‐Beta Peptide Forms Monomeric Complexes With CuII and ZnII Prior to Aggregation
- Christine Talmard, Luc Guilloreau, Y. Coppel, H. Mazarguil, P. Faller
- Chemistry
- 22 January 2007
The aggregation of the peptide amyloid-b (Ab) into fibrils is considered to be a key event in Alzheimer’s disease. In vivo, the most prevalent forms of Ab consist of 40 (Ab40) or 42 amino acids… Expand
Characterization of the ZnII Binding to the Peptide Amyloid‐β1–16 linked to Alzheimer's Disease
- Yasmina Mekmouche, Y. Coppel, +4 authors P. Faller
- Chemistry, Medicine
- Chembiochem : a European journal of chemical…
- 5 September 2005
Aggregation of the human peptide amyloid‐β (Aβ) is a key event in Alzheimer's disease (AD). Zinc ions play an important role in AD and in Aβ aggregation. In vitro, ZnII binds to Aβ and accelerates… Expand
NMR characterization of covalent adducts obtained by alkylation of heme with the antimalarial drug artemisinin
- A. Robert, Y. Coppel, B. Meunier
- Chemistry
- 15 November 2002
Abstract The peroxide function of artemisinin has been activated by iron(II)–heme generated in situ from iron(III)–protoporphyrin–IX or iron(III)–protoporphyrin–IX dimethylester and a reducing agent.… Expand
Solution conformation of an abasic DNA undecamer duplex d(CGCACXCACGC) x d(GCGTGTGTGCG): the unpaired thymine stacks inside the helix.
- Y. Coppel, N. Berthet, C. Coulombeau, J. García, J. Lhomme
- Chemistry, Medicine
- Biochemistry
- 22 April 1997
The three-dimensional structural analysis of DNA undecamer 5'd(C1G2C3A4C5X6C7A8C9G10C11)3', 3'd(G22C21G20T19G18T17G16T15G14C13G12)5' duplex in which the X residue is a modified abasic site… Expand
Amyloid-beta peptide forms monomeric complexes with Cu(II) and Zn(II) prior to aggregation.
- Christine Talmard, Luc Guilloreau, Y. Coppel, H. Mazarguil, P. Faller
- Medicine
- Chembiochem : a European journal of chemical…
- 2007
Aurasperone F – a new member of the naphtho-gamma-pyrone class isolated from a cultured microfungus, Aspergillus niger C-433
- N. Bouras, F. Mathieu, Y. Coppel, A. Lebrihi
- Chemistry, Medicine
- Natural product research
- 1 October 2005
A novel dimeric naphtho-γ-pyrone, named aurasperone F (1), was isolated from the fermentation broth of the culture extracts of Aspergillus niger C-433, isolated from grapes, along with the known… Expand
Dithiolopyrrolone antibiotic formation induced by adding valeric acid to the culture broth of Saccharothrix algeriensis.
- R. Merrouche, N. Bouras, +4 authors A. Lebrihi
- Biology, Medicine
- Journal of natural products
- 27 May 2010
Three new antibiotics were isolated from the fermentation broth of Saccharothrix algeriensis NRRL B-24137 and characterized as the dithiolopyrrolone derivatives valerylpyrrothine (1),… Expand
Purification and structure elucidation of three naturally bioactive molecules from the new terrestrial Streptomyces sp. TN17 strain
- S. Smaoui, L. Mellouli, A. Lebrihi, Y. Coppel, Lilia Fourati Ben Fguira, F. Mathieu
- Chemistry, Medicine
- Natural product research
- 16 February 2011
Thirty litres of fermentation broth was extracted from the newly isolated Streptomyces sp. strain TN17 and various separation and purification steps led to the isolation of three pure bioactive… Expand
Oxidation of photochromic spirooxazines by coinage metal cations. Part I. Reaction with AgNO3 : formation and characterisation of silver particles
- P. Uznanski, C. Amiens, B. Donnadieu, Y. Coppel, B. Chaudret
- Chemistry
- 2001
Thermal oxidation of the zwitterionic form of two photochromic spirooxazines: 1,3-dihydro-1,3,3-trimethylspiro(2H-indole-2,3′-[3H]naphth[2,1-b]-[1,4]oxazine)
(1) and… Expand