Indexed keywords
1 [(6 METHYL 2,2 DIOXIDO 1,2,3 OXATHIAZIN 4 YL)OXY]PROPAN 2 ONE;
2 [(6 METHYL 2,2 DIOXIDO 1,2,3 OXATHIAZIN 4YL)OXY] 1 PHENYLETHANONE;
3 (2 FLUOROBENZYL) 6 METHYL 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
3 (2,6 DIFLUOROBENZYL) 6 METHYL 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
3 (3 BROMOBENZYL) 6 METHYL 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
3 (3 FLUOROBENZYL) 6 METHYL 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
4 [(2 BROMOBENZYL)OXY] 6 METHYL 1,2,3 OXATHIAZINE 2,2 DIOXIDE;
4 [(3 FLUOROBENZYL)OXY] 6 METHYL 1,2,3 OXATHIAZINE 2,2 DIOXIDE;
4 [(6 METHYL 2,2 DIOXIDO 4 OXO 1,2,3 OXATHIAZIN 3(4H) YL)METHYL]BENZONITRILE;
6 METHYL 3 (2 NITROBENZYL) 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
6 METHYL 3 (2 OXO 2 PHENYLETHYL) 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
6 METHYL 3 (2 OXOPROPYL) 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
6 METHYL 3 (3 NITROBENZYL) 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
6 METHYL 3 (PROP 2 EN 1 YL) 1,2,3 OXATHIAZIN 4(3H)ONE 2,2 DIOXIDE;
6 METHYL 4 (PROP 2 EN 1 YLOXY) 1,2,3 OXATHIAZINE 2,2 DIOXIDE;
6 METHYL 4 (PROP 2 YN 1 YLOXY) 1,2,3 OXATHIAZINE 2,2 DIOXIDE;
6 METHYL 4 [(2 NITROBENZYL)OXY] 1,2,3 OXATHIAZINE 2,2 DIOXIDE;
6 METHYL 4 [(3 NITROBENZYL)OXY] 1,2,3 OXATHIAZINE 2,2 DIOXIDE;
ACESULFAME;
ACESULFAME DERIVATIVE;
ANTINEOPLASTIC AGENT;
CARBONATE DEHYDRATASE IX;
CARBONATE DEHYDRATASE XII;
E6 METHYL 3 [2 (3 NITROPHENYL) 2 OXOETHYL] 1,2,3 OXATHIAZIN 4 (3H)ONE;
ETHYL (6 METHYL 2,2 DIOXIDO 4 OXO 1,2,3 OXATHIAZIN 3(4H)YL)ACETATE;
ETHYL [(6 METHYL 2,2 DIOXIDO 1,2,3 OXATHIAZIN 4YL)OXY]ACETATE;
UNCLASSIFIED DRUG;
[(6 METHYL 2,2 DIOXIDO 1,2,3 OXATHIAZIN 4 YL)OXY]ACETONITRILE;
ACETOSULFAME;
CARBONATE DEHYDRATASE;
CARBONATE DEHYDRATASE INHIBITOR;
ISOPROTEIN;
SULFAMIC ACID;
SULFONIC ACID DERIVATIVE;
THIAZINE DERIVATIVE;
ARTICLE;
CANCER CELL LINE;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
MOLECULAR MODEL;
PHARMACOPHORE;
ANTAGONISTS AND INHIBITORS;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
METABOLISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
CARBONIC ANHYDRASE INHIBITORS;
CARBONIC ANHYDRASES;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HUMANS;
MOLECULAR STRUCTURE;
PROTEIN ISOFORMS;
STRUCTURE-ACTIVITY RELATIONSHIP;
SULFONIC ACIDS;
THIAZINES;
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