Compile Data Set for Download or QSAR
Found 38 with Last Name = 'bova' and Initial = 'f'
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322349((R)-Methyl4-(2-(3-((adamantan-1-ylcarbamoyloxy)met...)copy SMILEScopy InChI
Affinity DataKi:  2.60nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322349((R)-Methyl4-(2-(3-((adamantan-1-ylcarbamoyloxy)met...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50257018((E)-methyl4-(2-((R,Z)-3-((4-chloro-2-(trifluoromet...)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322342((R)-Methyl4-(2-(7-chloro-3-((4-chloro-2-(trifluoro...)copy SMILEScopy InChI
Affinity DataKi:  87nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50157741(CHEMBL374508 | E-64 | E64)copy SMILEScopy InChI
Affinity DataKi:  290nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322342((R)-Methyl4-(2-(7-chloro-3-((4-chloro-2-(trifluoro...)copy SMILEScopy InChI
Affinity DataKi:  460nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322343((R)-Methyl4-(2-(5-(4-bromophenyl)-3-((4-chloro-2-(...)copy SMILEScopy InChI
Affinity DataKi:  470nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50257018((E)-methyl4-(2-((R,Z)-3-((4-chloro-2-(trifluoromet...)copy SMILEScopy InChI
Affinity DataKi:  810nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322341(CHEMBL1171803 | Methyl4-(2-((R)-3-((4-chloro-2-(tr...)copy SMILEScopy InChI
Affinity DataKi:  870nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322346((R)-Methyl4-(2-(3-((naphthalen-1-ylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  930nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322343((R)-Methyl4-(2-(5-(4-bromophenyl)-3-((4-chloro-2-(...)copy SMILEScopy InChI
Affinity DataKi:  1.56E+3nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322341(CHEMBL1171803 | Methyl4-(2-((R)-3-((4-chloro-2-(tr...)copy SMILEScopy InChI
Affinity DataKi:  2.22E+3nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322345((R)-Methyl4-(2-(3-((4-methoxyphenylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  2.23E+3nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322347((R)-Methyl4-(2-(3-((butylcarbamoyloxy)methyl)-2-ox...)copy SMILEScopy InChI
Affinity DataKi:  2.70E+3nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322346((R)-Methyl4-(2-(3-((naphthalen-1-ylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  3.48E+3nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCysteine protease(Trypanosoma brucei rhodesiense)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322345((R)-Methyl4-(2-(3-((4-methoxyphenylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  4.30E+3nMAssay Description:Inhibition of Trypanosoma brucei rhodesiense rhodesain after 10 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322342((R)-Methyl4-(2-(7-chloro-3-((4-chloro-2-(trifluoro...)copy SMILEScopy InChI
Affinity DataKi:  6.10E+3nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50257018((E)-methyl4-(2-((R,Z)-3-((4-chloro-2-(trifluoromet...)copy SMILEScopy InChI
Affinity DataKi:  7.30E+3nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50257018((E)-methyl4-(2-((R,Z)-3-((4-chloro-2-(trifluoromet...)copy SMILEScopy InChI
Affinity DataKi:  8.40E+3nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322344((R)-Methyl4-(2-(3-((4-chloro-2-(trifluoromethyl)ph...)copy SMILEScopy InChI
Affinity DataKi:  1.09E+4nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322345((R)-Methyl4-(2-(3-((4-methoxyphenylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322346((R)-Methyl4-(2-(3-((naphthalen-1-ylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  1.22E+4nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322348((R)-Methyl4-(2-(3-((cyclohexylcarbamoyloxy)methyl)...)copy SMILEScopy InChI
Affinity DataKi:  1.24E+4nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322349((R)-Methyl4-(2-(3-((adamantan-1-ylcarbamoyloxy)met...)copy SMILEScopy InChI
Affinity DataKi:  1.37E+4nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322345((R)-Methyl4-(2-(3-((4-methoxyphenylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  1.51E+4nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322347((R)-Methyl4-(2-(3-((butylcarbamoyloxy)methyl)-2-ox...)copy SMILEScopy InChI
Affinity DataKi:  2.04E+4nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322346((R)-Methyl4-(2-(3-((naphthalen-1-ylcarbamoyloxy)me...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+4nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322342((R)-Methyl4-(2-(7-chloro-3-((4-chloro-2-(trifluoro...)copy SMILEScopy InChI
Affinity DataKi:  2.98E+4nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322341(CHEMBL1171803 | Methyl4-(2-((R)-3-((4-chloro-2-(tr...)copy SMILEScopy InChI
Affinity DataKi:  3.91E+4nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322344((R)-Methyl4-(2-(3-((4-chloro-2-(trifluoromethyl)ph...)copy SMILEScopy InChI
Affinity DataKi:  5.99E+4nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322349((R)-Methyl4-(2-(3-((adamantan-1-ylcarbamoyloxy)met...)copy SMILEScopy InChI
Affinity DataKi:  6.50E+4nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322348((R)-Methyl4-(2-(3-((cyclohexylcarbamoyloxy)methyl)...)copy SMILEScopy InChI
Affinity DataKi:  7.65E+4nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322348((R)-Methyl4-(2-(3-((cyclohexylcarbamoyloxy)methyl)...)copy SMILEScopy InChI
Affinity DataKi:  8.90E+4nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322344((R)-Methyl4-(2-(3-((4-chloro-2-(trifluoromethyl)ph...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetFalcipain 2(Plasmodium falciparum)
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322347((R)-Methyl4-(2-(3-((butylcarbamoyloxy)methyl)-2-ox...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of Plasmodium falciparum recombinant falcipain-2 after 10 minMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322343((R)-Methyl4-(2-(5-(4-bromophenyl)-3-((4-chloro-2-(...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+5nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322341(CHEMBL1171803 | Methyl4-(2-((R)-3-((4-chloro-2-(tr...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+5nMAssay Description:Inhibition of human cathepsin LMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed
TargetCathepsin B(Homo sapiens (Human))
Universit£ di Messina

Curated by ChEMBL
LigandPNGBDBM50322343((R)-Methyl4-(2-(5-(4-bromophenyl)-3-((4-chloro-2-(...)copy SMILEScopy InChI
Affinity DataKi: >1.50E+5nMAssay Description:Inhibition of human cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3G1RPubMed