Indexed keywords
2 (4 BROMOPHENYL) N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]ETHANAMINE;
3 OXOACYL ACYL CARRIER PROTEIN SYNTHASE;
3 OXOACYL ACYL CARRIER PROTEIN SYNTHASE III INHIBITOR;
4 BROMO N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]ANILINE;
4 CHLORO N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]ANILINE;
5 CHLORO N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]PYRIDIN 2 AMINE;
ACYLTRANSFERASE INHIBITOR;
ANTIBIOTIC AGENT;
KANAMYCIN B;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 1 (4 METHOXYPHENYL)METHANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 1 (FURAN 2 YL)METHANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 1 [4 (TRIFLUOROMETHYL)PHENYL]METHANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 1 PHENYLETHANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 1 PHENYLMETHANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 1H PYRAZOL 3 AMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 2 (3H INDOL 2 YL)ETHANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 4 FLUOROANILINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE] 4 METHOXYANILIN;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]ANILINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]BUTAN 1 AMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]CYCLOHEXANAMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]DODECAN 1 AMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]HEXADECAN 1 AMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]HEXAN 1 AMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]METHYLPROPAN 2 AMINE;
N [(3,4 DIHYDRO 2H BENZO[B][1,4]DIOXEPIN 7 YL)METHYLENE]OCTAN 1 AMINE;
SCHIFF BASE;
UNCLASSIFIED DRUG;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
BACILLUS SUBTILIS;
CONTROLLED STUDY;
DRUG CONFORMATION;
DRUG DESIGN;
DRUG POTENCY;
DRUG PROTEIN BINDING;
DRUG SYNTHESIS;
ENZYME ACTIVE SITE;
ENZYME INHIBITION;
ESCHERICHIA COLI;
IC 50;
MINIMUM INHIBITORY CONCENTRATION;
MOLECULAR DOCKING;
NONHUMAN;
PHARMACOPHORE;
PRIORITY JOURNAL;
PSEUDOMONAS FLUORESCENS;
STAPHYLOCOCCUS AUREUS;
STRUCTURE ACTIVITY RELATION;
3-OXOACYL-(ACYL-CARRIER-PROTEIN) SYNTHASE;
ANTI-BACTERIAL AGENTS;
BINDING SITES;
CATALYTIC DOMAIN;
ENZYME INHIBITORS;
ESCHERICHIA COLI;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR DOCKING SIMULATION;
SCHIFF BASES;
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