Indexed keywords
1 [4 (THYMIN 1 YL)BUT 2 ENYL] 5,6 DIHYDRO 1H IMIDAZO[4,5,1 IJ]QUINOLIN 2(4H) ONE;
1 [[4 (5 BROMOURACIL 1 YL)BUT 2 ENYL]] 5,6 DIHYDRO 1H,4H 1,2,5 THIADIAZOLO[4,3,2 IJ]QUINOLIN 2,2 DIOXIDE;
1 [[4 (THYMIN 1 YL)BUT 2 ENYL]] 5,6 DIHYDRO 1H,4H 1,2,5 THIADIAZOLO[4,3,2 IJ]QUINOLIN 2,2 DIOXIDE;
5 ACETAMIDO 1 [4 (THYMIN 1 YL)BUT 2 ENYL] 5,6 DIHYDRO 1H IMIDAZO[4,5,1 IJ]QUINOLIN 2(4H) ONE;
5 AMINO 1 [4 (THYMIN 1 YL)BUT 2 ENYL] 5,6 DIHYDRO 1H IMIDAZO[4,5,1 IJ]QUINOLIN 2(4H) ONE;
8 ACETAMIDO 1 [4 (THYMIN 1 YL)BUT 2 ENYL] 5,6 DIHYDRO 1H IMIDAZO[4,5,1 IJ]QUINOLIN 2(4H) ONE;
8 AMINO 1 [4 (THYMIN 1 YL)BUT 2 ENYL] 5,6 DIHYDRO 1H IMIDAZO[4,5,1 IJ]QUINOLIN 2(4H) ONE;
ACYCLIC NUCLEOSIDE;
ANTIMYCOBACTERIAL AGENT;
IMIDAZOQUINOLINE DERIVATIVE;
IODOBENZENE;
THYMIDINE PHOSPHATE;
UNCLASSIFIED DRUG;
UREA DERIVATIVE;
ACETYLATION;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
CATALYSIS;
CYCLIZATION;
DRUG DESIGN;
DRUG SYNTHESIS;
ENZYME INHIBITION;
MYCOBACTERIUM BOVIS;
MYCOBACTERIUM SMEGMATIS;
NONHUMAN;
OXIDATION;
DRUG DESIGN;
ENZYME INHIBITORS;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
MYCOBACTERIUM TUBERCULOSIS;
NUCLEOSIDE-PHOSPHATE KINASE;
NUCLEOSIDES;
QUINOLONES;
SOLUBILITY;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
4
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