Synthetic replacement of the methylamino group of neocarzinostatin chromophore with hydroxyl prohibits thiol activation in organic solvents and diminishes the rate and efficiency of thiol-promoted DNA cleavage in water
摘要:
A synthesis of the neocarzinostatin chromophore analog 2, in which the 2'-N-methylamino group of the natural product has been replaced by a hydroxyl group, is described. Thiol addition experiments in organic solvents and DNA-cleavage studies in aqueous solution are also described, and provide further support for the proposed participation of the carbohydrate methylamino group in neocarzinostatin activation. (C) 1999 Elsevier Science Ltd. All rights reserved.
Synthetic replacement of the methylamino group of neocarzinostatin chromophore with hydroxyl prohibits thiol activation in organic solvents and diminishes the rate and efficiency of thiol-promoted DNA cleavage in water
摘要:
A synthesis of the neocarzinostatin chromophore analog 2, in which the 2'-N-methylamino group of the natural product has been replaced by a hydroxyl group, is described. Thiol addition experiments in organic solvents and DNA-cleavage studies in aqueous solution are also described, and provide further support for the proposed participation of the carbohydrate methylamino group in neocarzinostatin activation. (C) 1999 Elsevier Science Ltd. All rights reserved.