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  1. Pubblicazioni

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

Rivista
Codice:
E060692
ISSN:
0223-5234
  • Dati Generali

Dati Generali

Pubblicazioni (19)

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6-Fluorophenylbenzohydrazides inhibit Mycobacterium tuberculosis growth through alteration of tryptophan biosynthesis
Articolo
Anti-Candida activity and cytotoxicity of a large library of new N-substituted-1,3-thiazolidin-4-one derivatives
Articolo
Biological evaluation and structure-activity relationships of imidazole-based compounds as antiprotozoal agents
Articolo
Comprehensive structural investigation of a potent and selective CXCR4 antagonist via crosslink modification
Articolo
Design and synthesis of 6-arylpyridine-tethered sulfonamides as novel selective inhibitors of carbonic anhydrase IX with promising antitumor features toward the human colorectal cancer
Articolo
Discovery of N-aryl-naphthylamines as in vitro inhibitors of the interaction between HIV integrase and the cofactor LEDGF/p75
Articolo
Disulfide bond replacement with non-reducible side chain to tail macrolactamization for the development of potent and selective CXCR4 peptide antagonists endowed with flanking binding sites
Articolo
Exploring the role of chloro and methyl substitutions in 2-phenylthiomethyl-benzoindole derivatives for 5-LOX enzyme inhibition
Articolo
Improving the solubility of a new class of antiinflammatory pharmacodynamic hybrids, that release nitric oxide and inhibit cycloxygenase-2 isoenzyme
Articolo
In vivo potent BM635 analogue with improved drug-like properties
Articolo
New deferiprone derivatives as multi-functional cholinesterase inhibitors. Design, synthesis and in vitro evaluation
Articolo
Protective effect of piceatannol and bioactive stilbene derivatives against hypoxia-induced toxicity in H9c2 cardiomyocytes and structural elucidation as 5-LOX inhibitors
Articolo
Pyridinyl- and pyridazinyl-3,6-diazabicyclo[3.1.1]heptane-anilines: Novel selective ligands with subnanomolar affinity for α4β2nACh receptors
Articolo
SAR analysis of new anti-TB drugs currently in pre-clinical and clinical development
Articolo
Synthesis and cytotoxicity of novel (thiazol-2-yl)hydrazine derivatives as promising anti-Candida agents
Articolo
Synthesis, anti-Candida activity, and cytotoxicity of new (4-(4-iodophenyl)thiazol-2-yl)hydrazine derivatives
Articolo
Synthesis, biological evaluation and quantitative structure-active relationships of 1,3-thiazolidin-4-one derivatives. A promising chemical scaffold endowed with high antifungal potency and low cytotoxicity
Articolo
Therapeutic potential for coxibs-nitric oxide releasing hybrids in cystic fibrosis
Articolo
Towards understanding the molecular recognition process in prokaryotic zinc-finger domain
Articolo
No Results Found
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