European journal of medicinal chemistry

Label

• European journal of medicinal chemistry (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• Fluorescence study for selecting specific ligands toward HER2 receptor: An example of receptor fragment approach (Articolo in rivista) (Prodotto della ricerca)
• 1,2-Dihydro-2-oxopyridine-3-carboxamides: the C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor. (Articolo in rivista) (Prodotto della ricerca)
• 2-Arylbenzofuran-based molecules as multipotent Alzheimer's disease modifying agents. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• New indolylarylsulfones as highly potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 1,2-Dihydro-2-oxopyridine-3-carboxamides: The C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Investigations on the 4-quinolone-3-carboxylic acid motif. 6. Synthesis and pharmacological evaluation of 7-substituted quinolone-3-carboxamide derivatives as high affinity ligands for cannabinoid receptors. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Design, synthesis and biological evaluation of biphenylamide derivatives as Hsp90 C-terminal inhibitors (Articolo in rivista) (Prodotto della ricerca)
• Novel pyrazole derivatives as neutral CB1 antagonists with significant activity towards food intake (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Design, synthesis and biological evaluation of biphenylamide derivatives as Hsp90 C-terminal inhibitors (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Tricyclic pyrazoles. Part 6. Benzofuro[3,2-c]pyrazole: A versatile architecture for CB2 selective ligands (Articolo in rivista) (Prodotto della ricerca)
• Resveratrol interferes with the aggregation of membrane-bound human-IAPP: A molecular dynamics study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Three-dimensional quantitative structure-selectivity relationships analysis guided rational design of a highly selective ligand for the cannabinoid receptor 2. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Synthesis and biological evaluation of novel delta (?) opioid receptor ligands with diazatricyclodecane skeletons (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)

Alternative label

• Eur. j. med. chem. (literal)
• European journal of medicinal chemistry. (literal)

Language

• mul (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn

• 1768-3254 (literal)

Preferred label

• European journal of medicinal chemistry (literal)

Publisher

• Elsevier [Paris] : FRA (literal)

Incoming links:

Rivista

• 2-Arylbenzofuran-based molecules as multipotent Alzheimer's disease modifying agents. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Investigations on the 4-quinolone-3-carboxylic acid motif. 6. Synthesis and pharmacological evaluation of 7-substituted quinolone-3-carboxamide derivatives as high affinity ligands for cannabinoid receptors. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Fluorescence study for selecting specific ligands toward HER2 receptor: An example of receptor fragment approach (Articolo in rivista) (Prodotto della ricerca)
• Novel pyrazole derivatives as neutral CB1 antagonists with significant activity towards food intake (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 1,2-Dihydro-2-oxopyridine-3-carboxamides: The C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Three-dimensional quantitative structure-selectivity relationships analysis guided rational design of a highly selective ligand for the cannabinoid receptor 2. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Resveratrol interferes with the aggregation of membrane-bound human-IAPP: A molecular dynamics study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Tricyclic pyrazoles. Part 6. Benzofuro[3,2-c]pyrazole: A versatile architecture for CB2 selective ligands (Articolo in rivista) (Prodotto della ricerca)
• New indolylarylsulfones as highly potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Design, synthesis and biological evaluation of biphenylamide derivatives as Hsp90 C-terminal inhibitors (Articolo in rivista) (Prodotto della ricerca)
• Design, synthesis and biological evaluation of biphenylamide derivatives as Hsp90 C-terminal inhibitors (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Synthesis and biological evaluation of novel delta (?) opioid receptor ligands with diazatricyclodecane skeletons (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 1,2-Dihydro-2-oxopyridine-3-carboxamides: the C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor. (Articolo in rivista) (Prodotto della ricerca)