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Volumn 23, Issue 5, 2008, Pages 629-640
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Design, synthesis and evaluation of new 6-substituted-5-benzyloxy-4- oxo-4H-pyran-2-carboxamides as potential Src inhibitors
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Author keywords
Amide bond formation; Cancer; Drug design; Pyran 4 one; Src
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Indexed keywords
3 BENZYLOXY 2 HYDROXYMETHYL 6 [(TETRAHYDRO 2H PYRAN 2 YLOXY)METHYL] 4H PYRAN 4 ONE;
3 BENZYLOXY 2,6 BIS(HYDROXYMETHYL) 4H PYRAN 4 ONE;
3 BENZYLOXY 6 HYDROXYMETHYL 2 (1 HYDROXY 2 METHYLPROPYL) 4H PYRAN 4 ONE;
3 BENZYLOXY 6 HYDROXYMETHYL 2 ISOBUTYL 4H PYRAN 4 ONE;
3 BENZYLOXY 6 HYDROXYMETHYL 2 METHYL 4H PYRAN 4 ONE;
3 HYDROXY 2 HYDROXYMETHYL 6 [(TETRAHYDRO 2H PYRAN 2 YLOXY)METHYL] 4H PYRAN 4 ONE;
3 HYDROXY 2,6 BIS(HYDROXYMETHYL) 4H PYRAN 4 ONE;
3 HYDROXY 6 HYDROXYMETHYL 2 (1 HYDROXY 2 METHYLPROPYL) 4H PYRAN 4 ONE;
5 BENZYLOXY 4 OXO 4H PYRAN 2 CARBOXAMIDE DERIVATIVE;
5 BENZYLOXY 4 OXO 4H PYRAN 2 CARBOXYLIC ACID;
5 BENZYLOXY 4 OXO N PHENYL 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 ISOBUTYL 4 OXO 4H PYRAN 2 CARBOXYLIC ACID;
5 BENZYLOXY 6 ISOBUTYL 4 OXO N PHENYL 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 ISOBUTYL N (2 CHLORO 6 METHYLPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 ISOBUTYL N (2 CHLOROPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 ISOBUTYL N (2,6 DICHLOROPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 ISOBUTYL N (2,6 DIMETHYLPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 METHYL 4 OXO N PHENYL 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 METHYL N (2 CHLORO 6 METHYLPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 METHYL N (2 CHLOROPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 METHYL N (2,6 DICHLOROPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY 6 METHYL N (2,6 DIMETHYLPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY N (2 CHLORO 6 METHYLPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY N (2 CHLOROPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY N (2,6 DICHLOROPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 BENZYLOXY N (2,6 DIMETHYLPHENYL) 4 OXO 4H PYRAN 2 CARBOXAMIDE;
5 HYDROXY 2 [(TETRAHYDRO 2H PYRAN 2 YLOXY)METHYL] 4H PYRAN 4 ONE;
PROTEIN KINASE INHIBITOR;
PROTEIN TYROSINE KINASE INHIBITOR;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ARTICLE;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
PRIORITY JOURNAL;
AMIDES;
ANTINEOPLASTIC AGENTS;
CATALYTIC DOMAIN;
DRUG DISCOVERY;
PROTEIN BINDING;
PROTEIN KINASE INHIBITORS;
SRC-FAMILY KINASES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 53249093798
PISSN: 14756366
EISSN: 14756374
Source Type: Journal
DOI: 10.1080/14756360802205299 Document Type: Article |
Times cited : (6)
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References (19)
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