Journal of Medicinal Chemistry p. 2094 - 2101 (1991)
Update date:2022-08-03
Topics:
Liu
Coward
Two diastereomers of the potent spermidine synthases inhibitor S-adenosyl-1,8-diamino-3-thiooctane have been prepared in high (>96% de) storeochemical purity. Two synthetic routes were investigated, one based on asymmetric induction and the other involving an enantiomeric synthesis. The latter route gave the desired products in >96% de, whereas the synthesis based on asymmetric induction resulted in only 80% in the final product. Evaluation of the two diastereomers as inhibitors of spermidine synthase showed that the R diastereomer is a more potent inhibitor than the S diastereomer.
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