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Volumn 44, Issue 2, 2009, Pages 511-518
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Synthesis and biological evaluation of a new family of anti-benzylanilinosulfonamides as CA IX inhibitors
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Author keywords
Carbonic anhydrase; Molecular modeling; Sulfonamide; Tumor associated isoform
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Indexed keywords
ANTI 3 [4 (AMINOSULFONYL)ANILINO] 2 HYDROXY 3 PHENYLPROPANOIC ACID;
ANTI 3 [4 (AMINOSULFONYL)ANILINO] 2 HYDROXY 3 PHENYLPROPANOIC ACID HYDROXYAMIDE POTASSIUM SALT;
ANTI 4 [(2,3 DIHYDROXY 1 PHENYLPROPYL)AMINO] 1 BENZENESULFONAMIDE;
ANTI 4 [[2 (BENZYLOXY) 3 HYDROXY 1 PHENYLPROPYL]AMINO]BENZENESULFONAMIDE;
ANTI BENZYLANILINOSULFONAMIDE DERIVATIVE;
CARBONATE DEHYDRATASE I;
CARBONATE DEHYDRATASE II;
CARBONATE DEHYDRATASE INHIBITOR;
CARBONATE DEHYDRATASE IX;
CARBONATE DEHYDRATASE IX INHIBITOR;
COBALT CHLORIDE;
ETHYL ANTI 3 [4 (AMINOSULFONYL)ANILINO] 2 BENZYLOXY 3 PHENYLPROPANOATE;
ETHYL ANTI 3 [4 (AMINOSULFONYL)ANILINO] 2 HYDROXY 3 PHENYLPROPANOATE;
ETHYLPHENYLGLYCIDATE;
GLYCINE DERIVATIVE;
ISOENZYME;
SULFANILAMIDE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CHEMICAL REACTION;
DERIVATIZATION;
DRUG PROTEIN BINDING;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVE SITE;
ENZYME INHIBITION;
ENZYME SPECIFICITY;
ENZYME STRUCTURE;
HUMAN;
MOLECULAR MODEL;
STEREOCHEMISTRY;
STRUCTURE ACTIVITY RELATION;
STRUCTURE ANALYSIS;
ANTIGENS, NEOPLASM;
BINDING SITES;
CARBONIC ANHYDRASE INHIBITORS;
CARBONIC ANHYDRASES;
HUMANS;
MODELS, MOLECULAR;
PROTEIN BINDING;
STRUCTURE-ACTIVITY RELATIONSHIP;
SULFANILAMIDES;
SULFONAMIDES;
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EID: 60149101971
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2008.03.034 Document Type: Article |
Times cited : (13)
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References (25)
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