Found 318 with Last Name = 'sosic' and Initial = 'i' 
Affinity DataKi: 2.50E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 3.30E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 3.30E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
TargetUDP-N-acetylglucosamine 1-carboxyvinyltransferase(Escherichia coli K-12 (Enterobacteria))
University of Ljubljana
University of Ljubljana
TargetUDP-N-acetylglucosamine 1-carboxyvinyltransferase 2(Staphylococcus aureus (Firmicutes))
University of Ljubljana
University of Ljubljana
Affinity DataKi: 3.60E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 4.00E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 4.40E+3nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 4.40E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 4.50E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 5.00E+3nMAssay Description:Uncompetitive inhibition of human recombinant cathepsin B endopeptidase activity using Z-Arg-Arg-AMC substrate assessed as inhibition constant for en...More data for this Ligand-Target Pair
Affinity DataKi: 5.40E+3nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 6.00E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 7.20E+3nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 7.40E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 8.00E+3nMAssay Description:Mixed inhibition of human recombinant cathepsin B exopeptidase activity using Abz-Gly-Ile-Val-Arg-Ala-Lys(Dnp)-OH substrate assessed as inhibition co...More data for this Ligand-Target Pair
Affinity DataKi: 8.95E+3nMAssay Description:Mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 9.00E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 9.10E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 9.50E+3nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 9.70E+3nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.01E+4nMAssay Description:Mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.02E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.03E+4nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 1.05E+4nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 1.08E+4nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 1.11E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.13E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.19E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.19E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.30E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.38E+4nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 1.48E+4nMAssay Description:Mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.56E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
TargetUDP-N-acetylglucosamine 1-carboxyvinyltransferase(Enterobacter cloacae (Enterobacteria))
University of Ljubljana
University of Ljubljana
Affinity DataKi: 1.66E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 1.90E+4nMAssay Description:Uncompetitive inhibition of human recombinant cathepsin B endopeptidase activity using Z-Arg-Arg-AMC substrate assessed as inhibition constant for en...More data for this Ligand-Target Pair
Affinity DataKi: 2.19E+4nMAssay Description:Partial mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as su...More data for this Ligand-Target Pair
Affinity DataKi: 2.30E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 2.30E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 2.40E+4nMAssay Description:Noncompetitive inhibition of human recombinant cathepsin B exopeptidase activity using Abz-Gly-Ile-Val-Arg-Ala-Lys(Dnp)-OH substrateMore data for this Ligand-Target Pair
Affinity DataKi: 2.43E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 2.83E+4nMAssay Description:Mixed-type inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 3.20E+4nMAssay Description:Uncompetitive inhibition of human recombinant cathepsin B endopeptidase activity using Z-Arg-Arg-AMC substrate assessed as inhibition constant for en...More data for this Ligand-Target Pair
Affinity DataKi: 3.40E+4nMAssay Description:Noncompetitive inhibition of human recombinant cathepsin B exopeptidase activity using Abz-Gly-Ile-Val-Arg-Ala-Lys(Dnp)-OH substrateMore data for this Ligand-Target Pair
Affinity DataKi: 3.41E+4nMAssay Description:Reversible inhibition of human recombinant cathepsin B assessed as formation of fluorescent degradation product AMC using Z-Arg-Arg-AMC as substrate ...More data for this Ligand-Target Pair
Affinity DataKi: 3.60E+4nMAssay Description:Mixed inhibition of human recombinant cathepsin B exopeptidase activity using Abz-Gly-Ile-Val-Arg-Ala-Lys(Dnp)-OH substrate assessed as inhibition co...More data for this Ligand-Target Pair
Affinity DataKi: 3.80E+4nMAssay Description:Noncompetitive inhibition of human recombinant cathepsin B exopeptidase activity using Abz-Gly-Ile-Val-Arg-Ala-Lys(Dnp)-OH substrateMore data for this Ligand-Target Pair
Affinity DataKi: 3.95E+4nMAssay Description:Mixed inhibition of cathepsin B (unknown origin) endopeptidase activity assessed as inhibition constant for enzyme-substrate-inhibitor complexMore data for this Ligand-Target Pair
3D Structure (crystal)