z-logo
Premium
Synthesis, Characterization and Antibacterial Activity of New 5‐( o ‐Chlorophenyl)‐3‐( o , p ‐dichlorophenyl)‐4,5‐dihydropyrazol‐1‐yl Oxime Ester Derivatives
Author(s) -
LIU XinHua,
SONG BaoAn,
ZHU HaiLiang,
ZUO RenBing
Publication year - 2008
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.200890095
Subject(s) - chemistry , dna gyrase , bacillus subtilis , oxime , antibacterial activity , minimum inhibitory concentration , escherichia coli , staphylococcus aureus , pseudomonas aeruginosa , in vitro , bacteria , stereochemistry , proton nmr , carbon 13 nmr , medicinal chemistry , biochemistry , genetics , biology , gene
Ten new 1‐(5‐(2‐chlorophenyl)‐3‐(2,4‐dichlorophenyl)‐4,5‐dihydropyrazol‐1‐yl) oxime ester derivatives were synthesized and characterized by elemental analysis, HRMS and 1 H NMR data. All the compounds have been screened for their antibacterial potential in vitro against Bacillus subtilis , Staphylococcus aureus , Escherichia coli and Pseudomonas aeruginosa . The results show that 7c and 7f possess significant activity with the minimum inhibitory concentrations (MIC) value of 1.562 µg/mL against all the four bacteria. Compounds 7c , 7d and 7f show moderate inhibition against the DNA gyrase (IC 50 =1.6–2.5 µg/mL). On the basis of the biological result, the structure‐activity relationship was discussed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom