109953-22-2Relevant academic research and scientific papers
INHIBITORS OF HUMAN LEUCOCYTE ELASTASE. PEPTIDES INCORPORATING AN &α-AZANORVALINE RESIDUE OR A THIOMETHYLENE LINKAGE IN PLACE OF A PEPTIDE BOND
Dutta, Anand S.,Giles, Michael, B.,Gormley, James J.,Williams, Joseph C.,Kusner, Edward J.
, p. 111 - 120 (2007/10/02)
Peptides containing an α-azanorvaline residue at the C-terminus and N- group at the N-terminus have been made as inhibitors of human leucocyte elastase.A number of analogues with an amide bond replaced by a thiomethylene group have also been prepared.The analogues were tested against leucocyte elastase using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as a substrate and the results were obtained as IC50 values.Both types of analogues inhibited the leucocyte elastase; the most potent of these was N--L-valyl-L-prolyl-α-azanorvaline phenyl ester ( 2 ) ( IC50 0.28 μM, Ki 0.02 μM ).
Inhibitors of Porcine Pancreatic Elastase. Peptides Incorporating &α-Aza-amino Acid Residues in the P1 Position
Dutta, Anand S.,Giles, Michael B.,Williams, Joseph C.
, p. 1655 - 1664 (2007/10/02)
Inhibitors of porcine pancreatic elastase based on one of the repeating peptide sequences (Gly-Val-Gly-Val-Ala) present in elastin have been prepared.Most of these contain an α-aza-amino acid benzyl ester group at the C-terminus and an N-(1-methoxycarbon
