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Compile Data Set for Download or QSAR

Found 26 hits Enz. Inhib. hit(s) with all data for assayid = 2 entry = 50014202   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cathepsin K


(Homo sapiens (Human))
BDBM50084655
PNG
(CHEMBL92708 | Calpeptin | Z-Leu-Nle-CHO | [(S)-1-(...)
Show SMILES CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)OCc1ccccc1)C=O |r|
Show InChI InChI=1S/C20H30N2O4/c1-4-5-11-17(13-23)21-19(24)18(12-15(2)3)22-20(25)26-14-16-9-7-6-8-10-16/h6-10,13,15,17-18H,4-5,11-12,14H2,1-3H3,(H,21,24)(H,22,25)/t17-,18-/m0/s1
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n/an/a 0.110n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139490
PNG
(2,2,4,4-tetramethylpentan-3-yl(S)-1,2-dioxo-1-((R)...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)(C)C)C(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C25H40N2O4/c1-9-10-16-19(27-23(30)31-22(24(3,4)5)25(6,7)8)20(28)21(29)26-17(2)18-14-12-11-13-15-18/h11-15,17,19,22H,9-10,16H2,1-8H3,(H,26,29)(H,27,30)/t17-,19+/m1/s1
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n/an/a 0.710n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139481
PNG
((R)-2,2-dimethyl-6-phenylhexan-3-yl(S)-1,2-dioxo-1...)
Show SMILES CCCC[C@H](NC(=O)O[C@H](CCCc1ccccc1)C(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C30H42N2O4/c1-6-7-20-25(27(33)28(34)31-22(2)24-18-12-9-13-19-24)32-29(35)36-26(30(3,4)5)21-14-17-23-15-10-8-11-16-23/h8-13,15-16,18-19,22,25-26H,6-7,14,17,20-21H2,1-5H3,(H,31,34)(H,32,35)/t22-,25+,26-/m1/s1
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n/an/a 0.790n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139496
PNG
((R)-4,4-dimethyl-1-phenylpentan-3-yl(S)-1,2-dioxo-...)
Show SMILES CCCC[C@H](NC(=O)O[C@H](CCc1ccccc1)C(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C29H40N2O4/c1-6-7-18-24(26(32)27(33)30-21(2)23-16-12-9-13-17-23)31-28(34)35-25(29(3,4)5)20-19-22-14-10-8-11-15-22/h8-17,21,24-25H,6-7,18-20H2,1-5H3,(H,30,33)(H,31,34)/t21-,24+,25-/m1/s1
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n/an/a 1.10n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50138842
PNG
(2,4-dimethylpentan-3-yl(S)-1,2-dioxo-1-((R)-1-phen...)
Show SMILES CCCC[C@H](NC(=O)OC(C(C)C)C(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C23H36N2O4/c1-7-8-14-19(25-23(28)29-21(15(2)3)16(4)5)20(26)22(27)24-17(6)18-12-10-9-11-13-18/h9-13,15-17,19,21H,7-8,14H2,1-6H3,(H,24,27)(H,25,28)/t17-,19+/m1/s1
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n/an/a 2.5n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139492
PNG
(CHEMBL355138 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OC(C1CCCC1)C1CCCC1)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C27H40N2O4/c1-3-4-18-23(24(30)26(31)28-19(2)20-12-6-5-7-13-20)29-27(32)33-25(21-14-8-9-15-21)22-16-10-11-17-22/h5-7,12-13,19,21-23,25H,3-4,8-11,14-18H2,1-2H3,(H,28,31)(H,29,32)/t19-,23+/m1/s1
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n/an/a 6.30n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139497
PNG
(3,3-dimethylbutan-2-yl(S)-1,2-dioxo-1-((R)-1-pheny...)
Show SMILES CCCC[C@H](NC(=O)OC(C)C(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C22H34N2O4/c1-7-8-14-18(24-21(27)28-16(3)22(4,5)6)19(25)20(26)23-15(2)17-12-10-9-11-13-17/h9-13,15-16,18H,7-8,14H2,1-6H3,(H,23,26)(H,24,27)/t15-,16?,18+/m1/s1
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n/an/a 20n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139485
PNG
(CHEMBL162041 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OC(CCC)CCC)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C23H36N2O4/c1-5-8-16-20(25-23(28)29-19(12-6-2)13-7-3)21(26)22(27)24-17(4)18-14-10-9-11-15-18/h9-11,14-15,17,19-20H,5-8,12-13,16H2,1-4H3,(H,24,27)(H,25,28)/t17-,20+/m1/s1
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n/an/a 32n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139487
PNG
(CHEMBL163185 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OCC(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C21H32N2O4/c1-6-7-13-17(23-20(26)27-14-21(3,4)5)18(24)19(25)22-15(2)16-11-9-8-10-12-16/h8-12,15,17H,6-7,13-14H2,1-5H3,(H,22,25)(H,23,26)/t15-,17+/m1/s1
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n/an/a 34n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50137790
PNG
(((S)-1-Formyl-pentyl)-carbamic acid tert-butyl est...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C=O
Show InChI InChI=1S/C11H21NO3/c1-5-6-7-9(8-13)12-10(14)15-11(2,3)4/h8-9H,5-7H2,1-4H3,(H,12,14)/t9-/m0/s1
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n/an/a 51n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139483
PNG
(CHEMBL163757 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OC(CC(C)C)CC(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C25H40N2O4/c1-7-8-14-22(27-25(30)31-21(15-17(2)3)16-18(4)5)23(28)24(29)26-19(6)20-12-10-9-11-13-20/h9-13,17-19,21-22H,7-8,14-16H2,1-6H3,(H,26,29)(H,27,30)/t19-,22+/m1/s1
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n/an/a 69n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139499
PNG
(CHEMBL351877 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OC(CC)CC)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C21H32N2O4/c1-5-8-14-18(23-21(26)27-17(6-2)7-3)19(24)20(25)22-15(4)16-12-10-9-11-13-16/h9-13,15,17-18H,5-8,14H2,1-4H3,(H,22,25)(H,23,26)/t15-,18+/m1/s1
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n/an/a 76n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139493
PNG
((S)-4,4-dimethyl-1-phenylpentan-3-yl(S)-1,2-dioxo-...)
Show SMILES CCCC[C@H](NC(=O)O[C@@H](CCc1ccccc1)C(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C29H40N2O4/c1-6-7-18-24(26(32)27(33)30-21(2)23-16-12-9-13-17-23)31-28(34)35-25(29(3,4)5)20-19-22-14-10-8-11-15-22/h8-17,21,24-25H,6-7,18-20H2,1-5H3,(H,30,33)(H,31,34)/t21-,24+,25+/m1/s1
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n/an/a 912n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139484
PNG
(CHEMBL162812 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C20H30N2O4/c1-6-7-13-16(22-19(25)26-20(3,4)5)17(23)18(24)21-14(2)15-11-9-8-10-12-15/h8-12,14,16H,6-7,13H2,1-5H3,(H,21,24)(H,22,25)/t14-,16+/m1/s1
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n/an/a 1.20E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139498
PNG
(CHEMBL163240 | [(S)-1-((R)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)O[C@@H](CCCc1ccccc1)C(C)(C)C)C(=O)C(=O)N[C@H](C)c1ccccc1
Show InChI InChI=1S/C30H42N2O4/c1-6-7-20-25(27(33)28(34)31-22(2)24-18-12-9-13-19-24)32-29(35)36-26(30(3,4)5)21-14-17-23-15-10-8-11-16-23/h8-13,15-16,18-19,22,25-26H,6-7,14,17,20-21H2,1-5H3,(H,31,34)(H,32,35)/t22-,25+,26+/m1/s1
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n/an/a 1.40E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139495
PNG
(((S)-1-Benzylaminooxalyl-pentyl)-carbamic acid ter...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NCc1ccccc1
Show InChI InChI=1S/C19H28N2O4/c1-5-6-12-15(21-18(24)25-19(2,3)4)16(22)17(23)20-13-14-10-8-7-9-11-14/h7-11,15H,5-6,12-13H2,1-4H3,(H,20,23)(H,21,24)/t15-/m0/s1
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n/an/a 2.90E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139480
PNG
((S)-tert-butyl 1,2-dioxo-1-(thiophen-2-ylmethylami...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NCc1cccs1
Show InChI InChI=1S/C17H26N2O4S/c1-5-6-9-13(19-16(22)23-17(2,3)4)14(20)15(21)18-11-12-8-7-10-24-12/h7-8,10,13H,5-6,9,11H2,1-4H3,(H,18,21)(H,19,22)/t13-/m0/s1
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n/an/a 3.40E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139489
PNG
(CHEMBL163555 | [(S)-1-((S)-1-Phenyl-ethylaminooxal...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)N[C@@H](C)c1ccccc1
Show InChI InChI=1S/C20H30N2O4/c1-6-7-13-16(22-19(25)26-20(3,4)5)17(23)18(24)21-14(2)15-11-9-8-10-12-15/h8-12,14,16H,6-7,13H2,1-5H3,(H,21,24)(H,22,25)/t14-,16-/m0/s1
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n/an/a 4.20E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139486
PNG
(((S)-1-Phenethylaminooxalyl-pentyl)-carbamic acid ...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C20H30N2O4/c1-5-6-12-16(22-19(25)26-20(2,3)4)17(23)18(24)21-14-13-15-10-8-7-9-11-15/h7-11,16H,5-6,12-14H2,1-4H3,(H,21,24)(H,22,25)/t16-/m0/s1
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n/an/a 5.00E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139500
PNG
(((S)-1-Aminooxalyl-pentyl)-carbamic acid tert-buty...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(N)=O
Show InChI InChI=1S/C12H22N2O4/c1-5-6-7-8(9(15)10(13)16)14-11(17)18-12(2,3)4/h8H,5-7H2,1-4H3,(H2,13,16)(H,14,17)/t8-/m0/s1
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n/an/a 5.90E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139491
PNG
(((S)-1-Phenylaminooxalyl-pentyl)-carbamic acid ter...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)Nc1ccccc1
Show InChI InChI=1S/C18H26N2O4/c1-5-6-12-14(20-17(23)24-18(2,3)4)15(21)16(22)19-13-10-8-7-9-11-13/h7-11,14H,5-6,12H2,1-4H3,(H,19,22)(H,20,23)/t14-/m0/s1
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n/an/a 6.30E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139482
PNG
(((S)-1-Isopropylaminooxalyl-pentyl)-carbamic acid ...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NC(C)C
Show InChI InChI=1S/C15H28N2O4/c1-7-8-9-11(12(18)13(19)16-10(2)3)17-14(20)21-15(4,5)6/h10-11H,7-9H2,1-6H3,(H,16,19)(H,17,20)/t11-/m0/s1
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n/an/a 9.10E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139494
PNG
(((S)-1-Ethylaminooxalyl-pentyl)-carbamic acid tert...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NCC
Show InChI InChI=1S/C14H26N2O4/c1-6-8-9-10(11(17)12(18)15-7-2)16-13(19)20-14(3,4)5/h10H,6-9H2,1-5H3,(H,15,18)(H,16,19)/t10-/m0/s1
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n/an/a 1.80E+4n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139479
PNG
(((S)-1-Methylaminooxalyl-pentyl)-carbamic acid ter...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NC
Show InChI InChI=1S/C13H24N2O4/c1-6-7-8-9(10(16)11(17)14-5)15-12(18)19-13(2,3)4/h9H,6-8H2,1-5H3,(H,14,17)(H,15,18)/t9-/m0/s1
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n/an/a 2.10E+4n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139488
PNG
(CHEMBL165345 | {(S)-1-[Methyl-((R)-1-phenyl-ethyl)...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)N(C)[C@H](C)c1ccccc1
Show InChI InChI=1S/C21H32N2O4/c1-7-8-14-17(22-20(26)27-21(3,4)5)18(24)19(25)23(6)15(2)16-12-10-9-11-13-16/h9-13,15,17H,7-8,14H2,1-6H3,(H,22,26)/t15-,17+/m1/s1
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n/an/a>1.00E+5n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50139501
PNG
(((S)-1-tert-Butylaminooxalyl-pentyl)-carbamic acid...)
Show SMILES CCCC[C@H](NC(=O)OC(C)(C)C)C(=O)C(=O)NC(C)(C)C
Show InChI InChI=1S/C16H30N2O4/c1-8-9-10-11(17-14(21)22-16(5,6)7)12(19)13(20)18-15(2,3)4/h11H,8-10H2,1-7H3,(H,17,21)(H,18,20)/t11-/m0/s1
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n/an/a>1.00E+5n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibitory activity against human cathepsin K


Bioorg Med Chem Lett 14: 719-22 (2004)


BindingDB Entry DOI: 10.7270/Q2QV3KX1
More data for this
Ligand-Target Pair