Answers are grounded in this paper and cite their sources.
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.
No takes yet. Share an insight, caveat, or question.
Motoyoshi et al. (2004) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: