P123
Int J. Antimicrob. Agents. 2013 Nov;42(5):410-5.
Deciphering azole resistance mechanisms with a focus on transcription factor-encoding genes TAC1, MRR1 and UPC2 in a set of fluconazole-resistant clinical isolates of Candida albicans.
P122
Bioorg. Med. Chem. Lett. 2013, 23, 6784-6788.
Synthesis of novel 7-substituted pyrido[2',3':4,5]furo[3,2-d]pyrimidin-4-amines and their N-aryl analogues and evaluation of their inhibitory activity against Ser/Thr Kinases.
P121
Eur. J. Med. Chem., 2013, 69, 823-832.
Synthesis and antiproliferative activity of benzofuran-based analogs of cercosporamide against non-small cell lung cancer cell lines.
P120
Clin. Microbiol. Infect. 2013 Mar 7.
Evaluation of two matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) systems for the identification of Candida species.
doi: 10.1111/1469-0691.12210.
P119
Journal of Natural Sciences Research, 2013, vol3 N°6 31-37.
Antiplasmodial efficacity of fruit extract and cladodes of Opuntia ficus-indica.
P118
J. Clin. Microbiol. 2013, Jun 19. PMID: 23784120.
Multilocus sequence typing of Pneumocystis jirovecii from clinical samples: how many and which loci ?
P117
Tetrahedron Lett., 2013, 54, 5378-5382.
Exploration of versatile reactions on 2-chloro-3-nitroimidazo[1,2-a]pyridine: expanding structural diversity of C2- and C3-functionalized imidazo[1,2-a]pyridines.
P116
Tetrahedron, 2013, 69, 3182-3191.
Novel synthesis of angular thiazolo[5,4-f] and [4,5-h]quinazolines, preparation of their linear thiazolo[4,5-g] and [5,4-g]quinazoline analogs.
P115
Phytochemistry Letters, 2013; 6(3):498-503.
Anti-AGEs and antiparasitic activity of an original prenylated isoflavonoid and flavanones isolated from Derris ferruginea.
P114
ACS Med. Chem. Lett., 2013, 4, 288-292.
Discovery of a novel broad-spectrum antifungal agent, derived from albaconazole.
P113
Eur. J. Med. Chem. 2013, 59, 283-295.
Synthesis and biological evaluation of N-aryl-7-methoxybenzo[b]furo[3,2-d]pyrimidin-4-amines and their N-arylbenzo[b]thieno[3,2-d]pyrimidin-4-amine analogues as dual inhibitors of CLK1 and DYRK1A kinases.
P112
J. Het. Chem., 2013, 50, 1187-1197.
Efficient new synthesis of N-arylbenzo[b]furo[3,2-d]pyrimidin-4-amines and their benzo[b]thieno[3,2-d]pyrimidin-4-amine analogues via a microwave-assisted Dimroth rearrangement.