|
Volumn 7, Issue 9, 2009, Pages 1868-1877
|
Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: Development of potent proteasome inhibitors by a stereochemical diversity-oriented strategy
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ACID EQUIVALENTS;
ACTIVE COMPOUNDS;
ANTI-CANCER DRUGS;
BIOLOGICAL EVALUATIONS;
DIVERSITY-ORIENTED APPROACHES;
LACTACYSTIN;
PROTEASOME INHIBITORS;
REGIO-ISOMERS;
REGIOISOMER;
SYNTHETIC PRECURSORS;
TARGET COMPOUNDS;
THREE-DIMENSIONAL STRUCTURES;
AMINATION;
AMINES;
AMINO ACIDS;
CHEMICAL COMPOUNDS;
ISOMERS;
LEAD COMPOUNDS;
ORGANIC ACIDS;
PROPANE;
STEREOCHEMISTRY;
THREE DIMENSIONAL;
STRATEGIC PLANNING;
BELACTOSIN A;
ENZYME INHIBITOR;
PEPTIDE;
PROTEASOME;
ARTICLE;
CELL SURVIVAL;
CHEMICAL STRUCTURE;
CHEMISTRY;
DRUG ANTAGONISM;
DRUG EFFECT;
HELA CELL;
HUMAN;
ISOMERISM;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
CELL SURVIVAL;
ENZYME INHIBITORS;
HELA CELLS;
HUMANS;
ISOMERISM;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
PEPTIDES;
PROTEASOME ENDOPEPTIDASE COMPLEX;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
|
EID: 64549086299
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/b900384c Document Type: Article |
Times cited : (41)
|
References (41)
|