Synthesis and anti-staphylococcal activity of new 4-diazopyrazole derivatives

European Journal of Medicinal Chemistry

Volumn 58, Issue , 2012, Pages 64-71

  Raimondi, Maria Valeria ^a   Maggio, Benedetta ^a   Raffa, Demetrio ^a   Plescia, Fabiana ^a   Cascioferro, Stella ^a   Cancemi, Gabriella ^a   Schillaci, Domenico ^a   Cusimano, Maria Grazia ^a   Vitale, Maria ^b   Daidone, Giuseppe ^a  

^a UNIVERSITY OF PALERMO   (Italy)

^b ISTITUTO ZOOPROFILATTICO SPERIMENTALE DELLA SICILIA A MIRRI   (Italy)

Author keywords

4 Diazopyrazoles; Anti biofilm activity; Anti staphylococcal activity

Indexed keywords

(4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)(PHENYLACETYL)AZANIDE; (4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)(PHENYLCARBAMOYL)AZANIDE; (4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)[(3,4 DICHLOROPHENYL)CARBAMOYL]AZANIDE; (4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)[(4 METHOXY 2 NITROPHENYL)CARBAMOYL]AZANIDE; (4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)[(4 METHOXYPHENYL)ACETYL]AZANIDE; (4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)[(4 NITROPHENYL)CARBAMOYL]AZANIDE; [(4 BUTOXY 2 NITROPHENYL)CARBAMOYL](4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)AZANIDE; [(4 CHLOROPHENYL)ACETYL](4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)AZANIDE; [(4 CHLOROPHENYL)CARBAMOYL](4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)AZANIDE; [[4 (BENZYLOXY) 3 NITROPHENYL]CARBAMOYL] (4 DIAZONIO 1,3 DIMETHYL 1H PYRAZOL 5 YL)AZANIDE; ACETIC ACID; ANTIBIOTIC AGENT; NITROUS ACID; PYRAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTISTAPHYLOCOCCAL ACTIVITY; ARTICLE; BACTERIAL STRAIN; BIOFILM; CHEMICAL REACTION; COLONY FORMING UNIT; DRUG SYNTHESIS; METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STAPHYLOCOCCUS AUREUS; STAPHYLOCOCCUS EPIDERMIDIS; STRUCTURE ACTIVITY RELATION; SUBSTITUTION REACTION;

ANTI-BACTERIAL AGENTS; AZO COMPOUNDS; BIOFILMS; DOSE-RESPONSE RELATIONSHIP, DRUG; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; PYRAZOLES; STAPHYLOCOCCUS AUREUS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84867620523     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2012.09.041     Document Type: Article

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