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Design and synthesis of 2,6-disubstituted-8-amino imidazo[1,2a]pyridines, a promising privileged structure.
Bioorg Med Chem. 2018 Jul 23;26(12):3296-3307. doi: 10.1016/j.bmc.2018.04.057. Epub 2018 Apr 30.
Bioorg Med Chem. 2018.
PMID: 29753566
Free article.
Design and synthesis of fused tetrahydroisoquinoline-iminoimidazolines.
Moas-Héloire V, Renault N, Batalha V, Arias AR, Marchivie M, Yous S, Deguine N, Buée L, Chavatte P, Blum D, Lopes L, Melnyk P, Agouridas L.
Moas-Héloire V, et al. Among authors: agouridas l.
Eur J Med Chem. 2015 Dec 1;106:15-25. doi: 10.1016/j.ejmech.2015.10.030. Epub 2015 Oct 19.
Eur J Med Chem. 2015.
PMID: 26513641
Free article.
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Design, synthesis and evaluation of 2-aryl benzoxazoles as promising hit for the A2A receptor.
Duroux R, Renault N, Cuelho JE, Agouridas L, Blum D, Lopes LV, Melnyk P, Yous S.
Duroux R, et al. Among authors: agouridas l.
J Enzyme Inhib Med Chem. 2017 Dec;32(1):850-864. doi: 10.1080/14756366.2017.1334648.
J Enzyme Inhib Med Chem. 2017.
PMID: 28661196
Free PMC article.
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Antagonists of the adenosine A2A receptor based on a 2-arylbenzoxazole scaffold: Investigation of the C5- and C7-positions to enhance affinity.
Duroux R, Agouridas L, Renault N, El Bakali J, Furman C, Melnyk P, Yous S.
Duroux R, et al. Among authors: agouridas l.
Eur J Med Chem. 2018 Jan 20;144:151-163. doi: 10.1016/j.ejmech.2017.12.007. Epub 2017 Dec 5.
Eur J Med Chem. 2018.
PMID: 29268131
Free article.
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