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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 388.9
BDBM50365012

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 7 hits in this display   
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
Lysosomal Pro-X carboxypeptidase


(Homo sapiens (Human))
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
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n/an/a 31n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PrCP using Mca-Ala-Pro-Lys(Dnp)-OH as substrate after 30 mins by fluorescence analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair
Lysosomal Pro-X carboxypeptidase


(Homo sapiens (Human))
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
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n/an/a 31n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PrCP using Mca-Ala-Pro-Lys(Dnp)-OH as substrate after 30 mins by fluorescence analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair
Lysosomal Pro-X carboxypeptidase


(Mus musculus)
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
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n/an/a 146n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of mouse recombinant PrCP using Mca-Ala-Pro-Lys(Dnp)-OH as substrate after 30 mins by fluorescence analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair
Lysosomal Pro-X carboxypeptidase


(Mus musculus)
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
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n/an/a 146n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of mouse recombinant PrCP using Mca-Ala-Pro-Lys(Dnp)-OH as substrate after 30 mins by fluorescence analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair
Lysosomal Pro-X carboxypeptidase


(Homo sapiens (Human))
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
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B.MOAD
antibodypedia
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PC sid
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Article
PubMed
n/an/a 223n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PrCP using Mca-Ala-Pro-Lys(Dnp)-OH as substrate after 30 mins by fluorescence analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair
Lysosomal Pro-X carboxypeptidase


(Mus musculus)
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
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Article
PubMed
n/an/a 2.21E+3n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of mouse recombinant PrCP assessed as angiotensin 3 cleavage after 8 mins by LC/MS analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair
Lysosomal Pro-X carboxypeptidase


(Mus musculus)
BDBM50365012
PNG
(CHEMBL1950916)
Show SMILES C[C@H](N(C)c1cc(ncn1)N1CCCC(C1)C(C)(C)O)c1ccc(Cl)cc1 |r|
Show InChI InChI=1S/C21H29ClN4O/c1-15(16-7-9-18(22)10-8-16)25(4)19-12-20(24-14-23-19)26-11-5-6-17(13-26)21(2,3)27/h7-10,12,14-15,17,27H,5-6,11,13H2,1-4H3/t15-,17?/m0/s1
Reactome pathway
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UniProtKB/SwissProt

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CHEMBL
PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 2.21E+3n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of mouse recombinant PrCP assessed as angiotensin 3 cleavage after 8 mins by LC/MS analysis


Bioorg Med Chem Lett 22: 1727-30 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.098
BindingDB Entry DOI: 10.7270/Q2GT5NNH
More data for this
Ligand-Target Pair