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12 similar compounds to monomer 50052693

Compile data set for download or QSAR
Wt: 344.3
BDBM16499
Wt: 386.4
BDBM16500
Wt: 374.3
BDBM16501
Wt: 370.3
BDBM16508
Wt: 314.3
BDBM16510
Purchase
Wt: 579.1
BDBM50406629
Wt: 376.8
BDBM50406632
Wt: 468.3
BDBM50406633
Wt: 421.3
BDBM50406635
Wt: 360.4
BDBM50406636
Wt: 445.7
BDBM50406637
Wt: 396.4
BDBM50406638

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 22 hits for monomerid = 16499,16500,16501,16508,16510,50406629,50406632,50406633,50406635,50406636,50406637,50406638   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cathepsin (B and K)


(Homo sapiens (Human))
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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PubMed
3.36n/an/an/an/an/an/an/an/a



National Chemical Laboratory (CSIR-NCL)

Curated by ChEMBL


Assay Description
Inhibition of cathepsin B


Bioorg Med Chem 19: 7129-35 (2011)


Article DOI: 10.1016/j.bmc.2011.09.058
BindingDB Entry DOI: 10.7270/Q2KW5GGT
More data for this
Ligand-Target Pair
Papain


(Carica papaya)
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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PubMed
2.40E+3n/an/an/an/an/an/a6.8n/a



University of Wisconsin

Curated by ChEMBL


Assay Description
Kinetic constant Apparent binding constant (Ki`) for the inhibition of papain conducted in 0.1 M phosphate, pH 6.8, at 30 degree C


J Med Chem 39: 3357-66 (1996)


Article DOI: 10.1021/jm950445b
BindingDB Entry DOI: 10.7270/Q2B56HTP
More data for this
Ligand-Target Pair
Cathepsin B


(Bos taurus (bovine))
BDBM16501
PNG
((2S)-2-[(2S,3R)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Show SMILES CCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)CC)C(O)=O
Show InChI InChI=1S/C16H26N2O8/c1-5-7(3)9(15(22)23)17-13(20)10(8(4)19)18-14(21)11-12(26-11)16(24)25-6-2/h7-12,19H,5-6H2,1-4H3,(H,17,20)(H,18,21)(H,22,23)/t7?,8-,9+,10+,11+,12+/m1/s1
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n/an/a 410n/an/an/an/a6.040



Osaka University of Pharmaceutical Sciences



Assay Description
Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...


J Mol Biol 362: 979-93 (2006)


Article DOI: 10.1016/j.jmb.2006.07.070
BindingDB Entry DOI: 10.7270/Q2DF6PGN
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin B


(Bos taurus (bovine))
BDBM16508
PNG
((2S)-1-[(2S,3S)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Show SMILES CCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)N1CCC[C@H]1C(O)=O
Show InChI InChI=1S/C17H26N2O7/c1-4-9(3)11(15(21)19-8-6-7-10(19)16(22)23)18-14(20)12-13(26-12)17(24)25-5-2/h9-13H,4-8H2,1-3H3,(H,18,20)(H,22,23)/t9-,10-,11-,12-,13-/m0/s1
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n/an/a 120n/an/an/an/a6.040



Osaka University of Pharmaceutical Sciences



Assay Description
Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...


J Mol Biol 362: 979-93 (2006)


Article DOI: 10.1016/j.jmb.2006.07.070
BindingDB Entry DOI: 10.7270/Q2DF6PGN
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin B


(Bos taurus (bovine))
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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n/an/a 40n/an/an/an/a6.040



Osaka University of Pharmaceutical Sciences



Assay Description
Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...


J Mol Biol 362: 979-93 (2006)


Article DOI: 10.1016/j.jmb.2006.07.070
BindingDB Entry DOI: 10.7270/Q2DF6PGN
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin (B and K)


(Homo sapiens (Human))
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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PCBioAssay
n/an/a 1.53n/an/an/an/a6.823



PCMD

Curated by PubChem BioAssay


Assay Description
Screening Center: Penn Center for Molecular Discovery Center Affiliation: University of Pennsylvania Network: Molecular Library Screening Center Netw...


PubChem Bioassay (2008)


BindingDB Entry DOI: 10.7270/Q25T3HTJ
More data for this
Ligand-Target Pair
Cathepsin L1


(Homo sapiens (Human))
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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n/an/a 3.61n/an/an/an/an/an/a



PCMD

Curated by PubChem BioAssay


Assay Description
Screening Center: Penn Center for Molecular Discovery Center Affiliation: University of Pennsylvania Network: Molecular Library Screening Center Netw...


PubChem Bioassay (2008)


BindingDB Entry DOI: 10.7270/Q27D2SJC
More data for this
Ligand-Target Pair
Cathepsin L1


(Homo sapiens (Human))
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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n/an/a<1.63n/an/an/an/an/an/a



PCMD

Curated by PubChem BioAssay


Assay Description
Screening Center: Penn Center for Molecular Discovery Center Affiliation: University of Pennsylvania Network: Molecular Library Screening Center Netw...


PubChem Bioassay (2009)


BindingDB Entry DOI: 10.7270/Q2WH2NDV
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406635
PNG
(CHEMBL63494)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCBr
Show InChI InChI=1S/C17H29BrN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406637
PNG
(CHEMBL61010)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCC(Cl)(Cl)Cl
Show InChI InChI=1S/C17H27Cl3N2O5/c1-9(2)5-6-21-14(23)11(7-10(3)4)22-15(24)12-13(27-12)16(25)26-8-17(18,19)20/h9-13H,5-8H2,1-4H3,(H,21,23)(H,22,24)/t11-,12-,13-/m0/s1
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n/an/a 700n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The ability of compound to inhibit calpain in a preparation of lysed platelets was measured with a caseinolytic assay(assay 1)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406632
PNG
(CHEMBL302897)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCCl
Show InChI InChI=1S/C17H29ClN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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n/an/a 2.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The ability of compound to inhibit calpain in a preparation of lysed platelets was measured with a caseinolytic assay(assay 1)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406636
PNG
(CHEMBL294046)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCF
Show InChI InChI=1S/C17H29FN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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n/an/a 500n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The ability of compound to inhibit calpain in a preparation of lysed platelets was measured with a caseinolytic assay(assay 1)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406629
PNG
(CHEMBL302443)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCC(Br)(Br)Br
Show InChI InChI=1S/C17H27Br3N2O5/c1-9(2)5-6-21-14(23)11(7-10(3)4)22-15(24)12-13(27-12)16(25)26-8-17(18,19)20/h9-13H,5-8H2,1-4H3,(H,21,23)(H,22,24)/t11-,12-,13-/m0/s1
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n/an/a 5.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406632
PNG
(CHEMBL302897)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCCl
Show InChI InChI=1S/C17H29ClN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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n/an/a 300n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406633
PNG
(CHEMBL64647)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCI
Show InChI InChI=1S/C17H29IN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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n/an/a 6.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406635
PNG
(CHEMBL63494)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCBr
Show InChI InChI=1S/C17H29BrN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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n/an/a 1.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The ability of compound to inhibit calpain in a preparation of lysed platelets was measured with a caseinolytic assay(assay 1)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406637
PNG
(CHEMBL61010)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCC(Cl)(Cl)Cl
Show InChI InChI=1S/C17H27Cl3N2O5/c1-9(2)5-6-21-14(23)11(7-10(3)4)22-15(24)12-13(27-12)16(25)26-8-17(18,19)20/h9-13H,5-8H2,1-4H3,(H,21,23)(H,22,24)/t11-,12-,13-/m0/s1
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n/an/a 1.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM16510
PNG
((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(O)=O
Show InChI InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1
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PubMed
n/an/a 40n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The ability of compound to inhibit calpain in a preparation of lysed platelets was measured with a caseinolytic assay(assay 1)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406638
PNG
(CHEMBL64174)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCC(F)(F)F
Show InChI InChI=1S/C17H27F3N2O5/c1-9(2)5-6-21-14(23)11(7-10(3)4)22-15(24)12-13(27-12)16(25)26-8-17(18,19)20/h9-13H,5-8H2,1-4H3,(H,21,23)(H,22,24)/t11-,12-,13-/m0/s1
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PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Calpain1/2


(Homo sapiens (Human))
BDBM50406636
PNG
(CHEMBL294046)
Show SMILES CC(C)CCNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1O[C@@H]1C(=O)OCCF
Show InChI InChI=1S/C17H29FN2O5/c1-10(2)5-7-19-15(21)12(9-11(3)4)20-16(22)13-14(25-13)17(23)24-8-6-18/h10-14H,5-9H2,1-4H3,(H,19,21)(H,20,22)/t12-,13-,14-/m0/s1
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PubMed
n/an/a 3.00E+3n/an/an/an/an/an/a



State University of New York Health Science Center

Curated by ChEMBL


Assay Description
The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)


J Med Chem 35: 2048-54 (1992)


Article DOI: 10.1021/jm00089a015
BindingDB Entry DOI: 10.7270/Q27M094H
More data for this
Ligand-Target Pair
Cathepsin B


(Bos taurus (bovine))
BDBM16499
PNG
((2S)-2-[(2S,3S)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Show SMILES CCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O
Show InChI InChI=1S/C15H24N2O7/c1-5-7(3)9(12(18)16-8(4)14(20)21)17-13(19)10-11(24-10)15(22)23-6-2/h7-11H,5-6H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t7-,8-,9-,10-,11-/m0/s1
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PubMed
n/an/a 23n/an/an/an/a6.040



Osaka University of Pharmaceutical Sciences



Assay Description
Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...


J Mol Biol 362: 979-93 (2006)


Article DOI: 10.1016/j.jmb.2006.07.070
BindingDB Entry DOI: 10.7270/Q2DF6PGN
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cathepsin B


(Bos taurus (bovine))
BDBM16500
PNG
((2S)-2-[(2S,3S)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Show SMILES CCOC(=O)[C@H]1O[C@@H]1C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C(C)CC)C(O)=O
Show InChI InChI=1S/C18H30N2O7/c1-6-9(4)11(15(21)20-12(17(23)24)10(5)7-2)19-16(22)13-14(27-13)18(25)26-8-3/h9-14H,6-8H2,1-5H3,(H,19,22)(H,20,21)(H,23,24)/t9-,10?,11-,12-,13-,14-/m0/s1
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n/an/a 24n/an/an/an/a6.040



Osaka University of Pharmaceutical Sciences



Assay Description
Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...


J Mol Biol 362: 979-93 (2006)


Article DOI: 10.1016/j.jmb.2006.07.070
BindingDB Entry DOI: 10.7270/Q2DF6PGN
More data for this
Ligand-Target Pair
3D
3D Structure (docked)