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BDBM50170882 CHEMBL3804856

SMILES: NC(CNC1CCCCC1)P(O)(=O)CC(Cc1ccccc1)C(O)=O

InChI Key: InChIKey=DDFITBNCTUGZCA-UHFFFAOYSA-N

Data: 5 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50170882   
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
Aminopeptidase N


(Homo sapiens (Human))
BDBM50170882
PNG
(CHEMBL3804856)
Show SMILES NC(CNC1CCCCC1)P(O)(=O)CC(Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C18H29N2O4P/c19-17(12-20-16-9-5-2-6-10-16)25(23,24)13-15(18(21)22)11-14-7-3-1-4-8-14/h1,3-4,7-8,15-17,20H,2,5-6,9-13,19H2,(H,21,22)(H,23,24)
PDB

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PC cid
PC sid
UniChem
PubMed
275n/an/an/an/an/an/an/an/a



Wroclaw University of Technology

Curated by ChEMBL


Assay Description
Inhibition of recombinant human alanyl aminopeptidase M1 using Ala-AMC as substrate preincubated for 30 to 60 mins followed by substrate addition mea...


Eur J Med Chem 117: 187-96 (2016)


BindingDB Entry DOI: 10.7270/Q2BC41F8
More data for this
Ligand-Target Pair
Aminopeptidase N


(Sus scrofa (Pig))
BDBM50170882
PNG
(CHEMBL3804856)
Show SMILES NC(CNC1CCCCC1)P(O)(=O)CC(Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C18H29N2O4P/c19-17(12-20-16-9-5-2-6-10-16)25(23,24)13-15(18(21)22)11-14-7-3-1-4-8-14/h1,3-4,7-8,15-17,20H,2,5-6,9-13,19H2,(H,21,22)(H,23,24)
PDB

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PC cid
PC sid
UniChem
PubMed
3.83E+3n/an/an/an/an/an/an/an/a



Wroclaw University of Technology

Curated by ChEMBL


Assay Description
Inhibition of pig kidney alanyl aminopeptidase M1 using Ala-AMC as substrate preincubated for 30 to 60 mins followed by substrate addition measured f...


Eur J Med Chem 117: 187-96 (2016)


BindingDB Entry DOI: 10.7270/Q2BC41F8
More data for this
Ligand-Target Pair
Aminopeptidase


(Homo sapiens (Human))
BDBM50170882
PNG
(CHEMBL3804856)
Show SMILES NC(CNC1CCCCC1)P(O)(=O)CC(Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C18H29N2O4P/c19-17(12-20-16-9-5-2-6-10-16)25(23,24)13-15(18(21)22)11-14-7-3-1-4-8-14/h1,3-4,7-8,15-17,20H,2,5-6,9-13,19H2,(H,21,22)(H,23,24)
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7.94E+3n/an/an/an/an/an/an/an/a



Wroclaw University of Technology

Curated by ChEMBL


Assay Description
Inhibition of human ERAP2 preincubated for 30 to 60 mins followed by addition of Arg-AMC as substrate measured for 15 mins by spectrofluorimetric met...


Bioorg Med Chem Lett 26: 4122-6 (2016)


Article DOI: 10.1016/j.bmcl.2016.06.062
BindingDB Entry DOI: 10.7270/Q2TT4SW1
More data for this
Ligand-Target Pair
Leucine aminopeptidase (LAP)


(Sus scrofa (Pig))
BDBM50170882
PNG
(CHEMBL3804856)
Show SMILES NC(CNC1CCCCC1)P(O)(=O)CC(Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C18H29N2O4P/c19-17(12-20-16-9-5-2-6-10-16)25(23,24)13-15(18(21)22)11-14-7-3-1-4-8-14/h1,3-4,7-8,15-17,20H,2,5-6,9-13,19H2,(H,21,22)(H,23,24)
GoogleScholar
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PC sid
UniChem
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2.83E+4n/an/an/an/an/an/an/an/a



Wroclaw University of Technology

Curated by ChEMBL


Assay Description
Inhibition of porcine kidney leucine aminopeptidase M17 using Leu-AMC as substrate preincubated for 30 to 60 mins followed by substrate addition meas...


Eur J Med Chem 117: 187-96 (2016)


BindingDB Entry DOI: 10.7270/Q2BC41F8
More data for this
Ligand-Target Pair
Aminopeptidase


(Homo sapiens (Human))
BDBM50170882
PNG
(CHEMBL3804856)
Show SMILES NC(CNC1CCCCC1)P(O)(=O)CC(Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C18H29N2O4P/c19-17(12-20-16-9-5-2-6-10-16)25(23,24)13-15(18(21)22)11-14-7-3-1-4-8-14/h1,3-4,7-8,15-17,20H,2,5-6,9-13,19H2,(H,21,22)(H,23,24)
PDB
MMDB

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PC cid
PC sid
UniChem
Article
PubMed
>2.50E+5n/an/an/an/an/an/an/an/a



Wroclaw University of Technology

Curated by ChEMBL


Assay Description
Inhibition of human ERAP1 preincubated for 30 to 60 mins followed by addition of Leu-AMC as substrate measured for 15 mins by spectrofluorimetric met...


Bioorg Med Chem Lett 26: 4122-6 (2016)


Article DOI: 10.1016/j.bmcl.2016.06.062
BindingDB Entry DOI: 10.7270/Q2TT4SW1
More data for this
Ligand-Target Pair