Indexed keywords
2 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)MALONIC ACID;
2 (5,9,13 TRIMETHYLTETRADECA 2,4,8,12 TETRAENOYLAMINO)MALONIC ACID;
3 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLIDENE)MALONIC ACID;
3 OXO 3 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLOXY)PROPANOIC ACID;
4 OXO 4 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLOXY)BUTANOIC ACID;
5,9,13 TRIMETHYL N (PHENYLSULFONYL)TETRADECA 4,8,12 TRIENAMIDE;
5,9,13 TRIMETHYLTETRADECA 2,4,8,12 TETRAENAMIDE;
5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENAMIDE;
5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYLSULFAMIC ACID;
8,12,16 TRIMETHYL 4 OXOHEPTADECA 7,11,15 TRIENOIC ACID;
9,13,17 TRIMETHYL 5 OXO OCTADECA 8,12,16 TRIENOIC ACID;
DIETHYL 2 (3 (4,4,5,5 TETRAMETHYL 1,3,2 DIOXABOROLAN2 YL)MALONATE;
DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 2,4,8,12 TETRAENOYLAMINO)MALONATE;
DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYL)PENTANEDIOATE;
DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYL)SUCCINATE;
DIETHYL 2 (5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENOYLAMINO)MALONATE;
DIETHYL 2 [3 (5 FORMYL 1 METHYL 1H IMIDAZOL 2 YL)ALLYL]MALONATE;
DIETHYL 2 [3 (5 FORMYL 1 METHYL 1H IMIDAZOL 2 YL)PROPYL)MALONATE;
DIETHYL 2 [3 [5 ((TERT BUTYLDIMETHYLSILYLOXY)METHYL) 1 METHYL 1H IMIDAZOL 2 YL)MALONATE;
DIETHYL 2 [3 [5 ((TERT BUTYLDIMETHYLSILYLOXY)METHYL) 1 METHYL 1H IMIDAZOL 2 YL]PROPYL]MALONATE;
DIMETHYL 2 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYL)MALONATE;
DIMETHYL 3 (3,7,11 TRIMETHYLDODECA 2,6,10 TRIENYLIDENE)MALONATE;
DOCETAXEL;
ETHYL 7,11,15 TRIMETHYL 3 OXOHEXADECA 6,10,14 TRIENOATE;
FARNESYL DIPHOSPHATE;
IMIDAZOLE;
MALONIC ACID;
N HYDROXY 5,9,13 TRIMETHYLTETRADECA 4,8,12 TRIENAMIDE;
PROTEIN FARNESYLTRANSFERASE INHIBITOR;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ARTICLE;
CONTROLLED STUDY;
DRUG SCREENING;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME BINDING;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
KINETICS;
BINDING SITES;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DRUG SCREENING ASSAYS, ANTITUMOR;
FARNESYLTRANSTRANSFERASE;
HUMANS;
KINETICS;
MOLECULAR STRUCTURE;
PARASITIC SENSITIVITY TESTS;
PLASMODIUM FALCIPARUM;
POLYISOPRENYL PHOSPHATES;
SESQUITERPENES;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
TRYPANOSOMA BRUCEI BRUCEI;
TRYPANOSOMA;
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Replacement of the succinyl moiety by a malonyl group does not change the activity (unpublished results).
Replacement of the succinyl moiety by a malonyl group does not change the activity (unpublished results).
50
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′ is the inhibitor dissociation constant of the enzyme-substrate-inhibitor complex.
′ is the inhibitor dissociation constant of the enzyme-substrate-inhibitor complex.
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