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Volumn 21, Issue 11, 2013, Pages 3080-3089
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Synthesis and evaluation of 7-chloro-4-(piperazin-1-yl)quinoline- sulfonamide as hybrid antiprotozoal agents
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Author keywords
Antiprotozoal agents; Cytotoxicity; Docking; Entamoeba histolytica; Homology modeling; Plasmodium falciparum; Sulfonamides
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Indexed keywords
4 [[4 (7 CHLOROQUINOLIN 4 YL)PIPERAZIN 1 YL]SULFONYL] N ACETYLANILINE;
7 CHLORO 4 (PIPERAZIN 1 YL)QUINOLINESULFONAMIDE DERIVATIVE;
7 CHLORO 4 [4 (2 NAPHTHYLSULFONYL)PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 (METHYLSULFONYL)PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 (PHENYLSULFONYL)PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 (PROPYLSULFONYL)PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 [(2,5 DICHLOROPHENYL)SULFONYL]PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 [(2-NITROPHENYL)SULFONYL]PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 [(4 CHLOROPHENYL)SULFONYL]PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 [(4 METHOXYPHENYL)SULFONYL]PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 [(4 METHYLPHENYL)SULFONYL]PIPERAZIN 1 YL]QUINOLINE;
7 CHLORO 4 [4 [(4 TERT BUTYLPHENYL)SULFONYL]PIPERAZIN 1 YL]QUINOLINE;
ANTIPROTOZOAL AGENT;
CHLOROQUINE;
DIHYDROPTEROATE SYNTHASE;
HEMATIN;
QUININE;
UNCLASSIFIED DRUG;
ANTIMALARIAL ACTIVITY;
ARTICLE;
CONTROLLED STUDY;
CRYSTAL STRUCTURE;
DRUG SCREENING;
DRUG SYNTHESIS;
ENTAMOEBA HISTOLYTICA;
ENZYME ACTIVE SITE;
HUMAN;
HUMAN CELL;
IC 50;
MOLECULAR DOCKING;
NONHUMAN;
PLASMODIUM FALCIPARUM;
AMINO ACID SEQUENCE;
ANTIPROTOZOAL AGENTS;
CELL SURVIVAL;
CHLOROQUINE;
CRYSTALLOGRAPHY, X-RAY;
DIHYDROPTEROATE SYNTHASE;
DRUG RESISTANCE;
ENTAMOEBA HISTOLYTICA;
ERYTHROCYTES;
HEMEPROTEINS;
HEMOLYSIS;
HUMANS;
MOLECULAR DOCKING SIMULATION;
MOLECULAR SEQUENCE DATA;
PIPERAZINES;
PLASMODIUM FALCIPARUM;
PROTOZOAN PROTEINS;
QUININE;
QUINOLINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
ENTAMOEBA HISTOLYTICA;
PLASMODIUM FALCIPARUM;
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EID: 84877795200
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2013.03.052 Document Type: Article |
Times cited : (54)
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References (48)
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