Thierry Cresteil
Overview
Explore the profile of Thierry Cresteil including associated specialties, affiliations and a list of published articles.
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68
Citations
752
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Recent Articles
1.
Djehal A, Krayem M, Najem A, Hammoud H, Cresteil T, Nebigil C, et al.
Eur J Med Chem
. 2018 Jul;
155:880-888.
PMID: 29960207
Prohibitins 1 and 2 (PHB1/2) are scaffold proteins that are involved in both melanogenesis and oncogenic pathways. We hypothesized that a PHB1 ligand, melanogenin, may display anti-cancer effects in addition...
2.
Mignani S, El Brahmi N, Cresteil T, Majoral J
Oncology
. 2018 Mar;
94(5):324-328.
PMID: 29533961
The metallo-phosphorus dendrimer 1G3-Cu (generation 3 dendrimer bearing 48 conjugated copper(II) on its surface) has antiproliferative activity related to its capacity to activate Bax translocation. In the present study, we...
3.
Mignani S, El Brahmi N, El Kazzouli S, Laurent R, Ladeira S, Caminade A, et al.
Mol Pharm
. 2017 Sep;
14(11):4087-4097.
PMID: 28960997
Original metallophosphorus dendrimers (generation 3, 48 terminal groups) have been prepared via the complexation of phosphorus dendrimers bearing imino-pyridino end groups with Au(III) or with both Au(III) and Cu(II). The...
4.
Mignani S, El Brahmi N, Eloy L, Poupon J, Nicolas V, Steinmetz A, et al.
Eur J Med Chem
. 2017 Mar;
132:142-156.
PMID: 28350998
A multivalent phosphorus dendrimer 1G and its corresponding Cu-complex, 1G-Cu have been recently identified as agents retaining high antiproliferative potency. This antiproliferative capacity was preserved in cell lines overexpressing the...
5.
Jourdan J, Since M, El Kihel L, Lecoutey C, Corvaisier S, Legay R, et al.
ChemMedChem
. 2017 Mar;
12(12):913-916.
PMID: 28342294
Herein we describe the drug design steps developed to increase the radical scavenging and β-amyloid aggregation inhibitory activities of a previously described series of benzylidenephenylpyrrolizinones. Among the newly synthesized derivatives,...
6.
Mignani S, El Brahmi N, El Kazzouli S, Eloy L, Courilleau D, Caron J, et al.
Eur J Med Chem
. 2016 Jul;
122:656-673.
PMID: 27448922
The well-known diuretic Ethacrynic acid (EA, Edecrin), showing low anti-proliferative activities, was chemically modified at different positions. The new EA derivatives have been tested in vitro in anti-proliferative assays on...
7.
Betzer J, Nuter F, Chtchigrovsky M, Hamon F, Kellermann G, Ali S, et al.
Bioconjug Chem
. 2016 Apr;
27(6):1456-70.
PMID: 27115175
G-quadruplex structures (G4) are promising anticancerous targets. A great number of small molecules targeting these structures have already been identified through biophysical methods. In cellulo, some of them are able...
8.
Jourdan J, Since M, El Kihel L, Lecoutey C, Corvaisier S, Legay R, et al.
Eur J Med Chem
. 2016 Apr;
114:365-79.
PMID: 27046230
This work describes the synthesis and the biological evaluation of novel benzylidenephenylpyrrolizinones as potential antioxidant, metal chelating or amyloid β (βA) aggregation inhibitors. Some derivatives exhibited interesting results in regard...
9.
Agnaniet H, Jolinom Mbot E, Keita O, Fehrentz J, Ankli A, Gallud A, et al.
BMC Complement Altern Med
. 2016 Feb;
16:71.
PMID: 26906899
Background: Diabetes mellitus is a metabolic disorder which is rising globally in rich and developing countries. In the African region this rate is the highest, with 20 million diagnosed diabetics....
10.
Fontaine F, Hequet A, Voisin-Chiret A, Bouillon A, Lesnard A, Cresteil T, et al.
Eur J Med Chem
. 2015 Mar;
95:185-98.
PMID: 25817769
In response to the extensive use of antibiotics, bacteria have evolved numerous mechanisms of defense against antimicrobial agents. Among them, extrusion of the antimicrobial agents outside the bacterial cell through...