1-Aminoisoquinoline as benzamidine isoster in the design and synthesis of orally active thrombin inhibitors.
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P. van Galen | C. V. van Boeckel | P J van Galen | J. Rewinkel | H. Lucas | A. Noach | T. van Dinther | A. Rood | A. Jenneboer | T G van Dinther | C A van Boeckel | J B Rewinkel | H Lucas | A B Noach | A M Rood | A J Jenneboer | P. J. van Galen
[1] Sangsoo Kim,et al. Rational design of selective thrombin inhibitors , 1997 .
[2] P. Artursson,et al. Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells. , 1991, Biochemical and biophysical research communications.
[3] Richard A. Engh,et al. DERIVATIVES OF 4-AMINO-PYRIDINE AS SELECTIVE THROMBIN INHIBITORS , 1997 .
[4] D. D. Perrin. Dissociation Constants of Organic Bases in Aqueous Solution , 1965 .
[5] J. Stürzebecher,et al. Cyclic amides of N alpha-arylsulfonylaminoacylated 4-amidinophenylalanine--tight binding inhibitors of thrombin. , 1983, Thrombosis research.
[6] P. Grootenhuis,et al. Peptide-derived transition state analogue inhibitors of thrombin; synthesis, activity and selectivity. , 1995, Bioorganic & medicinal chemistry.
[7] F. T. Tyson. Synthesis of Isoquinoline Acids , 1939 .