Laboratoire de Chimie de Coordination UPR 8241

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Laborde, J., Deraeve, C., de Mesquita Vieira, F. G., Sournia-Saquet, A., Rechignat, L., Drumond Villela, A., Lopes Abbadi, B., Souza Macchi, F., Pissinati, K., Bizarro, C. V., Machado, P., Augusto Basso, L., Pratviel, G., Gonzaga de França Lopes, L., Silva Sousa, E. H., et al. (2018). Synthesis and mechanistic investigation of iron(II) complexes of isoniazid and derivatives as a redox-mediated activation strategy for anti-tuberculosis therapy. J. Inorg. Biochem., 179, 71–81.
Paloque, L., Witkowski, B., Lelievre, J., Ouji, M., Ben Haddou, T., Ariey, F., Robert, A., Augereau, J. - M., Menard, D., Meunier, B., & Benoit-Vical, F. (2018). Endoperoxide-based compounds: cross-resistance with artemisinins and selection of a Plasmodium falciparum lineage with a K13 non-synonymous polymorphism. J. Antimicrob. Chemother., 73(2), 395–403.
Zhang, C., Bourgeade Delmas, S., Fernández Alvarez, A., Valentin, A., Hemmert, C., & Gornitzka, H. (2018). Synthesis, characterization, and antileishmanial activity of neutral N-heterocyclic carbenes gold(I) complexes. Eur. J. Med. Chem., 143, 1635–1643.
Zhang, W., Huang, D., Huang, M., Huang, J., Wang, D., Liu, X., Nguyen, M., Vendier, L., Mazères, S., Robert, A., Liu, Y., & Meunier, B. (2018). Preparation of tetradentate copper chelators as potential anti‐Alzheimer agents. ChemMedChem, 13(7), 684–704.
Zhang, W., Huang, M., Bijani, C., Liu, Y., Robert, A., & Meunier, B. (2018). Synthesis and characterization of copper-specific tetradendate ligands as potential treatment for Alzheimer's disease. C. R. Chimie, 21(5), 475–483.
Zhang, W., Liu, Y., Hureau, C., Robert, A., & Meunier, B. (2018). N4‐Tetradentate chelators efficiently regulate copper homeostasis and prevent ROS production induced by copper‐amyloid‐β1–16. Chem. – Eur. J., 24(31), 7825–7829.


Alassane, S. K., Nicolau-Travers, M. L., Menard, S., Andreoletti, O., Cambus, J. P., Gaudre, N., Wlodarczyk, M., Blanchard, N., Berry, A., Abbes, S., Colonge, D., Faye, B., Augereau, J. M., Lacroux, C., Iriart, X., et al. (2017). Young Sprague Dawley rats infected by Plasmodium berghei: A relevant experimental model to study cerebral malaria. Plos One, 12(7), e0181300.
Alvarez-Perez, M., Frutos, M., Viso, A., Fernandez de la Pradilla, R., de la Torre, M. C., Sierra, M. A., Gornitzka, H., & Hemmert, C. (2017). Gold(I)-catalyzed cycloisomerization-dimerization cascade of benzene-tethered 1,6-enynes. J. Org. Chem., 82(14), 7546–7554.
Avello, M. G., Frutos, M., de la Torre, M. C., Viso, A., Velado, M., de la Pradilla, R. F., Sierra, M. A., Gornitzka, H., & Hemmert, C. (2017). Chiral sulfur functional groups as definers of the chirality at the metal in Ir and Rh half-sandwich complexes: A combined CD/X-ray study. Chem. – Eur. J., 23(58), 14523–14531.
Fourmy, K., Gouygou, M., Dechy-Cabaret, O., & Benoit-Vical, F. (2017). Gold(I) complexes bearing phosphole ligands: Synthesis and antimalarial activity. C.R. Chimie, 20(4), 333–338.
Frutos, M., Ortuno, M. A., Lledos, A., Viso, A., Fernandez de la Pradilla, R., de la Torre, M. C., Sierra, M. A., Gornitzka, H., & Hemmert, C. (2017). Desulfinylation of Ag(I) sulfinyl mesoionic carbenes: Preparation of C-unsubstituted Au(I)–1,2,3-triazole carbene complexes. Org. Lett., 19(4), 822–825.
Laborde, J., Deraeve, C., & Bernardes-Genisson, V. (2017). Update of antitubercular prodrugs from a molecular perspective: Mechanisms of action, bioactivation pathways, and associated resistance. ChemMedChem, 12(20), 1657–1676.
Lee, V. Y., Ota, K., Ito, Y., Gapurenko, O. A., Sekiguchi, A., Minyaev, R. M., Minkin, V. I., & Gornitzka, H. (2017). Bis(stibahousene). J. Am. Chem. Soc., 139(39), 13897–13902.
Mvumbi, D. M., Bobanga, T. L., Kayembe, J. M. N., Mvumbi, G. L., Situakibanza, H. N. T., Benoit-Vical, F., Melin, P., De Mol, P., & Hayette, M. P. (2017). Molecular surveillance of Plasmodium falciparum resistance to artemisinin-based combination therapies in the Democratic Republic of Congo. Plos One, 12(6), e0179142.
Nguyen, M., Huang, M., Liu, Y., Meunier, B., & Robert, A. (2017). Is iron associated with amyloid involved in the oxidative stress of Alzheimer's disease? C. R. Chimie, 20(11), 987–989.
Nguyen, M., Meunier, B., & Robert, A. (2017). Catechol-based ligands as potential metal chelators inhibiting redox activity in Alzheimer's disease. Eur. J. Inorg. Chem., 2017(25), 3198–3204.
Nguyen, M., Vendier, L., Stigliani, J. - L., Meunier, B., & Robert, A. (2017). Structures of the copper and zinc complexes of PBT2, a chelating agent evaluated as potential drug for neurodegenerative diseases. Eur. J. Inorg. Chem., 2017(3), 600–608.
Vasquez-Ocmin, P., Haddad, M., Gadea, A., Jullian, V., Castillo, D., Paloque, L., Cerapio, J. P., Bourdy, G., & Sauvain, M. (2017). A new phthalide derivative from Peperomia nivalis. Nat. Prod. Res., 31(2), 138–142.
Zebiri, I., Haddad, M., Duca, L., Sauvain, M., Paloque, L., Cabanillas, B., Rengifo, E., Behr, J. - B., & Voutquenne-Nazabadioko, L. (2017). Biological activities of triterpenoids from Poraqueiba sericea stems. Nat. Prod. Res., 31(11), 1333–1338.
Zhang, D., Cochrane, J. R., Di Pietro, S., Guy, L., Gornitzka, H., Dutasta, J. - P., & Martinez, A. (2017). “Breathing” motion of a modulable molecular cavity. Chem. – Eur. J., 23(27), 6495–6498.