Indexed keywords
1 (3 CHLOROPHENYL) 2 (5 PHENYL 1,3,4 OXADIAZOL 2 YLTHIO)ETHANONE;
1 (3 CHLOROPHENYL) 2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 (3 FLUOROPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 (3 FLUOROPHENYL) 2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 (3 HYDROXYPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 (3 HYDROXYPHENYL) 2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 (3 METHOXYPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 (3 NITROPHENYL) 2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 (3,4 DICHLOROPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 (4 BROMOPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 (4 BROMOPHENYL) 2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 (4 CHLOROPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 (4 CHLOROPHENYL) 2 [[5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 (4 METHOXYPHENYL) 2 [(5 PHENYL 1,3,4 OXADIAZOL 2 YL)SULFANYL] 1 ETHANONE;
1 [1,1' BIPHENYL] 4 YL 2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
1 [1,1' BIPHENYL] 4 YL 2 [[5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 ETHANONE;
2 [5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YLTHIO] 1 (3 HYDROXYPHENYL)ETHANONE;
2 [[5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 (2 METHOXYPHENYL) 1 ETHANONE;
2 [[5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 (3 FLUOROPHENYL) 1 ETHANONE;
2 [[5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 (3 METHOXYPHENYL) 1 ETHANONE;
2 [[5 (4 CHLOROPHENYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 (4 METHOXYPHENYL) 1 ETHANONE;
2 [[5 [4 (BENZYLOXY)PHENYL] 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 (2 METHOXYPHENYL) 1 ETHANONE;
2 [[5 [4 (BENZYLOXY)PHENYL] 1,3,4 OXADIAZOL 2 YL]SULFANYL] 1 (4 METHOXYPHENYL) 1 ETHANONE;
3 [2 [[5 (3 PYRIDINYL) 1,3,4 OXADIAZOL 2 YL]SULFANYL]ACETYL] 2H CHROMEN 2 ONE;
ALPHA GLUCOSIDASE INHIBITOR;
CARBONATE DEHYDRATASE II;
OXADIAZOLE DERIVATIVE;
PHOSPHODIESTERASE I;
THIADIAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ALPHA GLUCOSIDASE;
CARBONATE DEHYDRATASE;
CARBONATE DEHYDRATASE INHIBITOR;
GLYCOSIDASE INHIBITOR;
PHOSPHODIESTERASE INHIBITOR;
3T3 CELL LINE;
ANIMAL CELL;
ARTICLE;
COMPETITIVE INHIBITION;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DIABETIC PATIENT;
DISSOCIATION CONSTANT;
DRUG CYTOTOXICITY;
DRUG EFFICACY;
DRUG INDICATION;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
ENZYME KINETICS;
ENZYME SPECIFICITY;
HYPERGLYCEMIA;
IC50;
IN VITRO STUDY;
MTT ASSAY;
NONHUMAN;
POSTPRANDIAL STATE;
RAT;
ANIMAL;
ANTAGONISTS AND INHIBITORS;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
METABOLISM;
MOUSE;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
3T3 CELLS;
ALPHA-GLUCOSIDASES;
ANIMALS;
CARBONIC ANHYDRASE INHIBITORS;
CARBONIC ANHYDRASES;
DOSE-RESPONSE RELATIONSHIP, DRUG;
GLYCOSIDE HYDROLASE INHIBITORS;
MICE;
MOLECULAR STRUCTURE;
OXADIAZOLES;
PHOSPHODIESTERASE I;
PHOSPHODIESTERASE INHIBITORS;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIADIAZOLES;
2
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