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Volumn 22, Issue 13, 2014, Pages 3441-3448
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Discovery of novel oxindole derivatives as potent α-glucosidase inhibitors
a
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Author keywords
Acarbose; Docking studies; Oxindole; Glucosidase
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Indexed keywords
3 (2 CHLOROBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (2 HYDROXY 3 METHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (2 HYDROXY 5 METHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (2 NITROBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (2,3,4 TRIMETHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (2,4 DICHLOROBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (3 ETHOXY 2 HYDROXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (3 HYDROXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (3 METHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (3,4 DIHYDROXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (3,4 DIMETHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (4 ETHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (4 HYDROXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (4 METHOXYBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (4 METHYLBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (4 NITROBENZYLIDENE) 6 CHLOROINDOLIN 2 ONE;
3 (ANTHRACEN 10 YLMETHYLENE) 6 CHLOROINDOLIN 2 ONE;
3 BENZYLIDENE 6 CHLOROINDOLIN 2 ONE;
3 [4 (DIMETHYLAMINO)BENZYLIDENE] 6 CHLOROINDOLIN 2 ONE;
3 [4 (METHYLTHIO)BENZYLIDENE] 6 CHLOROINDOLIN 2 ONE;
4 [(6 CHLORO 2 OXOINDOLIN 3 YLIDENE)METHYL]BENZALDEHYDE;
6 CHLORO 3 (FURAN 2 YLMETHYLENE)INDOLIN 2 ONE;
6 CHLORO 3 (NAPHTHALENE 1 YLMETHYLENE)INDOLIN 2 ONE;
6 CHLORO 3 OXINDOLE DERIVATIVE;
6 CHLOROOXINDOLE;
ACARBOSE;
ALPHA GLUCOSIDASE INHIBITOR;
INDOLE DERIVATIVE;
PIPERIDINE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ALPHA GLUCOSIDASE;
CHLORINATED HYDROCARBON;
ENZYME INHIBITOR;
ARTICLE;
CHEMICAL REACTION;
CONTROLLED STUDY;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ELECTROSPRAY MASS SPECTROMETRY;
ENZYME INHIBITION;
ENZYME INHIBITOR INTERACTION;
IC 50;
IN VITRO STUDY;
MOLECULAR DOCKING;
NUCLEOTIDE SEQUENCE;
PROTON NUCLEAR MAGNETIC RESONANCE;
SACCHAROMYCES CEREVISIAE;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
DRUG DEVELOPMENT;
ENZYMOLOGY;
METABOLISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
ALPHA-GLUCOSIDASES;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DISCOVERY;
ENZYME INHIBITORS;
HYDROCARBONS, CHLORINATED;
INDOLES;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
SACCHAROMYCES CEREVISIAE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84901929620
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2014.04.033 Document Type: Article |
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Times cited : (65)
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References (26)
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