1-Aminoisoquinoline as benzamidine isoster in the design and synthesis of orally active thrombin inhibitors
作者:J.B.M. Rewinkel、H. Lucas、P.J.M. van Galen、A.B.J. Noach、T.G. van Dinther、A.M.M. Rood、A.J.S.M. Jenneboer、C.A.A. van Boeckel
DOI:10.1016/s0960-894x(99)00069-4
日期:1999.3
Replacement of the highly basic benzamidine moiety of NAPAP by the moderately basic 1-aminoisoquinoline moiety resulted in thrombin inhibitors with improved selectivity towards trypsin and enhanced Caco-2 cell permeability. (C) 1999 Elsevier Science Ltd. All rights reserved.