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19 similar compounds to monomer 50138844

Compile data set for download or QSAR
Wt: 434.5
BDBM50138847
Wt: 420.5
BDBM50138848
Wt: 408.5
BDBM50138849
Wt: 380.4
BDBM50138851
Wt: 394.5
BDBM50138855
Wt: 420.5
BDBM50138865
Wt: 422.5
BDBM50138872
Wt: 448.5
BDBM50138877
Wt: 446.5
BDBM50154146
Wt: 448.5
BDBM50154150
Wt: 432.5
BDBM50154152
Wt: 420.5
BDBM50154153
Wt: 392.4
BDBM50154158
Wt: 418.5
BDBM50154160
Wt: 366.4
BDBM50154161
Displayed 1 to 15 (of 19 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 23 hits for monomerid = 50138847,50138848,50138849,50138851,50138855,50138865,50138872,50138877,50154146,50154150,50154152,50154153,50154158,50154160,50154161   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cathepsin K


(Rattus norvegicus)
BDBM50138848
PNG
(CHEMBL155592 | [(S)-1-(2-Cyclopropylmethyl-2H-pyra...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1CC1CC1
Show InChI InChI=1S/C22H36N4O4/c1-6-7-8-17(24-22(29)30-20(14(2)3)15(4)5)19(27)21(28)25-18-11-12-23-26(18)13-16-9-10-16/h11-12,14-17,20H,6-10,13H2,1-5H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 1.70E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154161
PNG
(CHEMBL360630 | [1-(2-Methyl-2H-pyrazol-3-ylaminoox...)
Show SMILES CCCC[C@H](NC(=O)OCC(C)(C)CC)C(=O)C(=O)Nc1ccnn1C
Show InChI InChI=1S/C18H30N4O4/c1-6-8-9-13(20-17(25)26-12-18(3,4)7-2)15(23)16(24)21-14-10-11-19-22(14)5/h10-11,13H,6-9,12H2,1-5H3,(H,20,25)(H,21,24)/t13-/m0/s1
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n/an/a 1.20E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138849
PNG
(CHEMBL157224 | [(S)-1-(2-Isopropyl-2H-pyrazol-3-yl...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C(C)C
Show InChI InChI=1S/C21H36N4O4/c1-8-9-10-16(23-21(28)29-19(13(2)3)14(4)5)18(26)20(27)24-17-11-12-22-25(17)15(6)7/h11-16,19H,8-10H2,1-7H3,(H,23,28)(H,24,27)/t16-/m0/s1
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n/an/a 1.00E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138851
PNG
(CHEMBL152633 | [(S)-1-(2-Methyl-2H-pyrazol-3-ylami...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C
Show InChI InChI=1S/C19H32N4O4/c1-7-8-9-14(21-19(26)27-17(12(2)3)13(4)5)16(24)18(25)22-15-10-11-20-23(15)6/h10-14,17H,7-9H2,1-6H3,(H,21,26)(H,22,25)/t14-/m0/s1
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n/an/a 32n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138855
PNG
(CHEMBL345136 | [(S)-1-(2-Ethyl-2H-pyrazol-3-ylamin...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1CC
Show InChI InChI=1S/C20H34N4O4/c1-7-9-10-15(22-20(27)28-18(13(3)4)14(5)6)17(25)19(26)23-16-11-12-21-24(16)8-2/h11-15,18H,7-10H2,1-6H3,(H,22,27)(H,23,26)/t15-/m0/s1
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n/an/a 1.50E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138855
PNG
(CHEMBL345136 | [(S)-1-(2-Ethyl-2H-pyrazol-3-ylamin...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1CC
Show InChI InChI=1S/C20H34N4O4/c1-7-9-10-15(22-20(27)28-18(13(3)4)14(5)6)17(25)19(26)23-16-11-12-21-24(16)8-2/h11-15,18H,7-10H2,1-6H3,(H,22,27)(H,23,26)/t15-/m0/s1
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n/an/a 26n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138865
PNG
(CHEMBL155148 | [(S)-1-(2-Cyclobutyl-2H-pyrazol-3-y...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C1CCC1
Show InChI InChI=1S/C22H36N4O4/c1-6-7-11-17(24-22(29)30-20(14(2)3)15(4)5)19(27)21(28)25-18-12-13-23-26(18)16-9-8-10-16/h12-17,20H,6-11H2,1-5H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 1.10E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138847
PNG
(CHEMBL155123 | [(S)-1-(2-Cyclopentyl-2H-pyrazol-3-...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C1CCCC1
Show InChI InChI=1S/C23H38N4O4/c1-6-7-12-18(25-23(30)31-21(15(2)3)16(4)5)20(28)22(29)26-19-13-14-24-27(19)17-10-8-9-11-17/h13-18,21H,6-12H2,1-5H3,(H,25,30)(H,26,29)/t18-/m0/s1
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n/an/a 1.10E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138851
PNG
(CHEMBL152633 | [(S)-1-(2-Methyl-2H-pyrazol-3-ylami...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C
Show InChI InChI=1S/C19H32N4O4/c1-7-8-9-14(21-19(26)27-17(12(2)3)13(4)5)16(24)18(25)22-15-10-11-20-23(15)6/h10-14,17H,7-9H2,1-6H3,(H,21,26)(H,22,25)/t14-/m0/s1
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n/an/a 1.70E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138872
PNG
(CHEMBL346739 | [(S)-1-(2-Isobutyl-2H-pyrazol-3-yla...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1CC(C)C
Show InChI InChI=1S/C22H38N4O4/c1-8-9-10-17(24-22(29)30-20(15(4)5)16(6)7)19(27)21(28)25-18-11-12-23-26(18)13-14(2)3/h11-12,14-17,20H,8-10,13H2,1-7H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 2.70E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138848
PNG
(CHEMBL155592 | [(S)-1-(2-Cyclopropylmethyl-2H-pyra...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1CC1CC1
Show InChI InChI=1S/C22H36N4O4/c1-6-7-8-17(24-22(29)30-20(14(2)3)15(4)5)19(27)21(28)25-18-11-12-23-26(18)13-16-9-10-16/h11-12,14-17,20H,6-10,13H2,1-5H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 27n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138877
PNG
(CHEMBL346102 | [(S)-1-(2-Cyclohexyl-2H-pyrazol-3-y...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C1CCCCC1
Show InChI InChI=1S/C24H40N4O4/c1-6-7-13-19(26-24(31)32-22(16(2)3)17(4)5)21(29)23(30)27-20-14-15-25-28(20)18-11-9-8-10-12-18/h14-19,22H,6-13H2,1-5H3,(H,26,31)(H,27,30)/t19-/m0/s1
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n/an/a 22n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Rattus norvegicus)
BDBM50138877
PNG
(CHEMBL346102 | [(S)-1-(2-Cyclohexyl-2H-pyrazol-3-y...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C1CCCCC1
Show InChI InChI=1S/C24H40N4O4/c1-6-7-13-19(26-24(31)32-22(16(2)3)17(4)5)21(29)23(30)27-20-14-15-25-28(20)18-11-9-8-10-12-18/h14-19,22H,6-13H2,1-5H3,(H,26,31)(H,27,30)/t19-/m0/s1
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n/an/a>1.20E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of cystiene protease cathepsin K of rat


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138872
PNG
(CHEMBL346739 | [(S)-1-(2-Isobutyl-2H-pyrazol-3-yla...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1CC(C)C
Show InChI InChI=1S/C22H38N4O4/c1-8-9-10-17(24-22(29)30-20(15(4)5)16(6)7)19(27)21(28)25-18-11-12-23-26(18)13-14(2)3/h11-12,14-17,20H,8-10,13H2,1-7H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 39n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138865
PNG
(CHEMBL155148 | [(S)-1-(2-Cyclobutyl-2H-pyrazol-3-y...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C1CCC1
Show InChI InChI=1S/C22H36N4O4/c1-6-7-11-17(24-22(29)30-20(14(2)3)15(4)5)19(27)21(28)25-18-12-13-23-26(18)16-9-8-10-16/h12-17,20H,6-11H2,1-5H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 15n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138849
PNG
(CHEMBL157224 | [(S)-1-(2-Isopropyl-2H-pyrazol-3-yl...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C(C)C
Show InChI InChI=1S/C21H36N4O4/c1-8-9-10-16(23-21(28)29-19(13(2)3)14(4)5)18(26)20(27)24-17-11-12-22-25(17)15(6)7/h11-16,19H,8-10H2,1-7H3,(H,23,28)(H,24,27)/t16-/m0/s1
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n/an/a 17n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154146
PNG
(CHEMBL362292 | [1-(2-Cyclohexyl-2H-pyrazol-3-ylami...)
Show SMILES CCCC[C@H](NC(=O)OCC1(CC)CCC1)C(=O)C(=O)Nc1ccnn1C1CCCCC1
Show InChI InChI=1S/C24H38N4O4/c1-3-5-12-19(26-23(31)32-17-24(4-2)14-9-15-24)21(29)22(30)27-20-13-16-25-28(20)18-10-7-6-8-11-18/h13,16,18-19H,3-12,14-15,17H2,1-2H3,(H,26,31)(H,27,30)/t19-/m0/s1
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n/an/a 58n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154150
PNG
(CHEMBL363950 | {1-[2-(3,3-Dimethyl-butyl)-2H-pyraz...)
Show SMILES CCCC[C@H](NC(=O)OCC1(CC)CCC1)C(=O)C(=O)Nc1ccnn1CCC(C)(C)C
Show InChI InChI=1S/C24H40N4O4/c1-6-8-10-18(26-22(31)32-17-24(7-2)12-9-13-24)20(29)21(30)27-19-11-15-25-28(19)16-14-23(3,4)5/h11,15,18H,6-10,12-14,16-17H2,1-5H3,(H,26,31)(H,27,30)/t18-/m0/s1
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n/an/a 71n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154152
PNG
(CHEMBL184212 | [1-(2-Cyclopentyl-2H-pyrazol-3-ylam...)
Show SMILES CCCC[C@H](NC(=O)OCC1(CC)CCC1)C(=O)C(=O)Nc1ccnn1C1CCCC1
Show InChI InChI=1S/C23H36N4O4/c1-3-5-11-18(25-22(30)31-16-23(4-2)13-8-14-23)20(28)21(29)26-19-12-15-24-27(19)17-9-6-7-10-17/h12,15,17-18H,3-11,13-14,16H2,1-2H3,(H,25,30)(H,26,29)/t18-/m0/s1
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n/an/a 83n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154153
PNG
(CHEMBL185403 | [1-(2-Isobutyl-2H-pyrazol-3-ylamino...)
Show SMILES CCCC[C@H](NC(=O)OCC1(CC)CCC1)C(=O)C(=O)Nc1ccnn1CC(C)C
Show InChI InChI=1S/C22H36N4O4/c1-5-7-9-17(24-21(29)30-15-22(6-2)11-8-12-22)19(27)20(28)25-18-10-13-23-26(18)14-16(3)4/h10,13,16-17H,5-9,11-12,14-15H2,1-4H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 76n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154160
PNG
(CHEMBL361911 | [1-(2-Cyclopropylmethyl-2H-pyrazol-...)
Show SMILES CCCC[C@H](NC(=O)OCC1(CC)CCC1)C(=O)C(=O)Nc1ccnn1CC1CC1
Show InChI InChI=1S/C22H34N4O4/c1-3-5-7-17(24-21(29)30-15-22(4-2)11-6-12-22)19(27)20(28)25-18-10-13-23-26(18)14-16-8-9-16/h10,13,16-17H,3-9,11-12,14-15H2,1-2H3,(H,24,29)(H,25,28)/t17-/m0/s1
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n/an/a 51n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50154158
PNG
(CHEMBL425535 | [1-(2-Methyl-2H-pyrazol-3-ylaminoox...)
Show SMILES CCCC[C@H](NC(=O)OCC1(CC)CCCC1)C(=O)C(=O)Nc1ccnn1C
Show InChI InChI=1S/C20H32N4O4/c1-4-6-9-15(17(25)18(26)23-16-10-13-21-24(16)3)22-19(27)28-14-20(5-2)11-7-8-12-20/h10,13,15H,4-9,11-12,14H2,1-3H3,(H,22,27)(H,23,26)/t15-/m0/s1
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n/an/a 135n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory potency against human Cathepsin K


J Med Chem 47: 5049-56 (2004)


Article DOI: 10.1021/jm0400799
BindingDB Entry DOI: 10.7270/Q27H1J39
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138847
PNG
(CHEMBL155123 | [(S)-1-(2-Cyclopentyl-2H-pyrazol-3-...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)Nc1ccnn1C1CCCC1
Show InChI InChI=1S/C23H38N4O4/c1-6-7-12-18(25-23(30)31-21(15(2)3)16(4)5)20(28)22(29)26-19-13-14-24-27(19)17-10-8-9-11-17/h13-18,21H,6-12H2,1-5H3,(H,25,30)(H,26,29)/t18-/m0/s1
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n/an/a 20n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Concentration required to inhibit 50% of cysteine protease cathepsin K of human


J Med Chem 47: 588-99 (2004)


Article DOI: 10.1021/jm030373l
BindingDB Entry DOI: 10.7270/Q29S1QF7
More data for this
Ligand-Target Pair