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Volumn 97, Issue , 2015, Pages 32-41
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Design, synthesis and antibacterial activity of cinnamaldehyde derivatives as inhibitors of the bacterial cell division protein FtsZ
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Author keywords
Antibacterial activity; Cell division inhibitory activity; Cinnamaldehyde derivatives; Design; FtsZ; Synthesis
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Indexed keywords
(4 METHOXYPHENYL)CINNAMAMIDE;
1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL) 3 (3,4,5 TRIMETHOXYPHENYL)PROP 2 EN 1 ONE;
1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL) 3 (4 NITROPHENYL)PROP 2 EN 1 ONE;
1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL) 3 PSHENYLPROP 2 EN 1 ONE;
3 (2 CHLOROPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1YL)PROP 2 EN 1 ONE;
3 (2 METHOXYPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL)PROP 2 EN 1 ONE;
3 (2,4 DICHLOROPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL)PROP 2 EN 1 ONE;
3 (2,4 DICHLOROPHENYL) N (4 METHOXYPHENYL)ACRYLAMIDE;
3 (2,4 DICHLOROPHENYL) N HEXYLACRYLAMIDE;
3 (2,4 DICHLOROPHENYL) N ISOPROPYLACRYLAMIDE;
3 (2,4 DICHLOROPHENYL) N PROPYLACRYLAMIDE;
3 (3,4 DIMETHOXYPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL)PROP 2 EN 1 ONE;
3 (3,4 DIMETHOXYPHENYL) N (PROP 2 YNYL)ACRYLAMIDE;
3 (4 CHLOROPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1YL)PROP 2 EN 1 ONE;
3 (4 FLUOROPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1YL)PROP 2 EN 1 ONE;
3 (4 METHOXYPHENYL) 1 (2 METHYL 1H BENZO[D]IMIDAZOL 1 YL)PROP 2 EN 1 ONE;
3 (4 METHOXYPHENYL) N (PYRIDIN 3 YL)ACRYLAMIDE;
3 (4 NITROPHENYL) N (PROP 2 YNYL)ACRYLAMIDE;
3 (4 NITROPHENYL) N PROPYLACRYLAMIDE;
AMINO ACID;
ANTIBIOTIC AGENT;
CINNAMALDEHYDE DERIVATIVE;
FTSZ PROTEIN;
GUANOSINE TRIPHOSPHATASE;
N BUTYL 3 (2,4 DICHLOROPHENYL)ACRYLAMIDE;
N BUTYL 3 (4 CYANOPHENYL)ACRYLAMIDE;
N BUTYL 3 (4 NITROPHENYL)ACRYLAMIDE;
N ISOPROPYL 3 (4 NITROPHENYL)ACRYLAMIDE;
N [3 (2 METHYL 1H IMIDAZOL 1 YL) 5 (TRIFLUOROMETHYL)PHENYL] 3 (4 NITROPHENYL)ACRYLAMIDE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ACROLEIN;
ANTIINFECTIVE AGENT;
BACTERIAL PROTEIN;
CINNAMALDEHYDE;
CYTOSKELETON PROTEIN;
FTSZ PROTEIN, BACTERIA;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
BACTERIAL CELL;
BACTERIAL CLEARANCE;
BACTERIAL STRAIN;
BINDING SITE;
CELL DIVISION;
CONCENTRATION (PARAMETERS);
DRUG DESIGN;
DRUG EFFICACY;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME INHIBITION;
HYDROGEN BOND;
HYDROPHOBICITY;
IN VITRO STUDY;
LIGHT SCATTERING;
MITOSIS INHIBITION;
NONHUMAN;
PROTEIN POLYMERIZATION;
STAPHYLOCOCCUS AUREUS;
ANALOGS AND DERIVATIVES;
ANTAGONISTS AND INHIBITORS;
CHEMICAL STRUCTURE;
CHEMISTRY;
DRUG EFFECTS;
SYNTHESIS;
ACROLEIN;
ANTI-BACTERIAL AGENTS;
BACTERIAL PROTEINS;
CELL DIVISION;
CYTOSKELETAL PROTEINS;
DRUG DESIGN;
MOLECULAR STRUCTURE;
STAPHYLOCOCCUS AUREUS;
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EID: 84928666657
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2015.04.048 Document Type: Article |
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Times cited : (66)
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References (29)
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