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Volumn 19, Issue 15, 2011, Pages 4460-4472
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Design, synthesis and evaluation of N-benzoylindazole derivatives and analogues as inhibitors of human neutrophil elastase
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Author keywords
1 Benzoylindazoles; Human neutrophil elastase; Indazoles; Inhibitors; Structure activity relationship
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Indexed keywords
1 (2 METHOXYBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID PHENYLAMIDE;
1 (3 AMINOBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (3 AMINOBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID PHENYLAMIDE;
1 (3 METHOXYBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (3 METHOXYBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID METHYL ESTER;
1 (3 METHOXYBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID PHENYLAMIDE;
1 (3 METHYLBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID METHYL ESTER;
1 (3 METHYLBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID PROPYL ESTER;
1 (3 TERT BUTOXYCARBONYLAMINO BENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (3,4,5 TRIMETHOXYBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (4 CYANOBENZOYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (NAPHTHALENE 1 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (PYRIDINE 4 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (PYRIDINE 4 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID PHENYLAMIDE;
1 (THIOPHENE 3 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 (THIOPHENE 3 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID METHYL ESTER;
1 (THIOPHENE 3 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID PHENYLAMIDE;
1 (THIOPHENE 3 CARBONYL) 1H INDAZOLE 3 CARBOXYLIC ACID PROPYL ESTER;
1 BENZOYL 1H INDAZOLE 3 CARBOXYLIC ACID METHYL ESTER;
1 BENZOYL 1H INDAZOLE 3 CARBOXYLIC ACID PHENYLAMIDE;
1 BUTYRYL 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 CYCLOPENTANECARBONYL 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1 PROPIONYL 1H INDAZOLE 3 CARBOXYLIC ACID ETHYL ESTER;
1H INDAZOLE 3 CARBOXYLIC ACID 2,2,2 TRIFLUOROETHYL ESTER;
[3 (3 PHENYLCARBAMOYL INDAZOLE 1 CARBONYL)PHENYL]CARBAMIC ACID TERT BUTYL ESTER;
INDAZOLE DERIVATIVE;
LEUKOCYTE ELASTASE INHIBITOR;
N BENZOYLINDAZOLE DERIVATIVE;
SIVELESTAT;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ARTICLE;
BINDING SITE;
BIOLOGICAL ACTIVITY;
CONCENTRATION RESPONSE;
DRUG DESIGN;
DRUG SCREENING;
DRUG STABILITY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
ENZYME SPECIFICITY;
HUMAN;
IC 50;
MOLECULAR DOCKING;
MOLECULAR MODEL;
STRUCTURE ACTIVITY RELATION;
DRUG DESIGN;
ENZYME INHIBITORS;
HUMANS;
INDAZOLES;
INHIBITORY CONCENTRATION 50;
LEUKOCYTE ELASTASE;
MODELS, MOLECULAR;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 79960558163
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2011.06.036 Document Type: Article |
Times cited : (33)
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References (52)
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