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Biosci Biotechnol Biochem ; 68(10): 2178-82, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15502365

ABSTRACT

The structure-activity relationship for FR901464, a potent cell-cycle inhibitor, was examined by synthesizing its analogs. A versatile method for converting FR901464 was devised. This method made it possible to synthesize biologically active FR901464-biotin conjugates which could be used to isolate the binding proteins.


Subject(s)
Biotin/chemistry , Biotinylation , Cell Cycle/drug effects , Pyrans/chemistry , Spiro Compounds/chemistry , Pyrans/analysis , Pyrans/chemical synthesis , Pyrans/pharmacology , Spiro Compounds/analysis , Spiro Compounds/chemical synthesis , Spiro Compounds/pharmacology , Structure-Activity Relationship
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