BindingDB logo
myBDB logout

PubMed code 20022504

Compile data set for download or QSAR
Found 9 hits of Enzyme Inhibition Constant Data   
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
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM21281
PNG
((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)
Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r|
Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
PDB
UniChem

Patents


Similars

PDB
Article
PubMed
2.10n/an/an/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human recombinant CB2 receptor expressed in HEK293 cells after 90 mins


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM21281
PNG
((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)
Show SMILES Cc1c(C(=O)c2cccc3ccccc23)c2cccc3OC[C@@H](CN4CCOCC4)n1c23 |r|
Show InChI InChI=1S/C27H26N2O3/c1-18-25(27(30)22-9-4-7-19-6-2-3-8-21(19)22)23-10-5-11-24-26(23)29(18)20(17-32-24)16-28-12-14-31-15-13-28/h2-11,20H,12-17H2,1H3/t20-/m1/s1
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
PDB
UniChem

Patents


Similars

Article
PubMed
9.20n/an/an/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human recombinant CB1 receptor expressed in HEK293 cells after 90 mins


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50171299
PNG
(CHEMBL190662 | Cyclohexanecarboxylic acid pentadec...)
Show SMILES CCCCCCCCCCCCCCCNC(=O)C1CCCCC1
Show InChI InChI=1S/C22H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-23-22(24)21-18-15-14-16-19-21/h21H,2-20H2,1H3,(H,23,24)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.50E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of NAAA


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50309176
PNG
(CHEMBL190429 | N-Pentadecyl-benzamide | N-pentadec...)
Show SMILES CCCCCCCCCCCCCCCNC(=O)c1ccccc1
Show InChI InChI=1S/C22H37NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-23-22(24)21-18-15-14-16-19-21/h14-16,18-19H,2-13,17,20H2,1H3,(H,23,24)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 8.30E+3n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of NAAA


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50309177
PNG
(CHEMBL590884 | cyclopentyl palmitate)
Show SMILES CCCCCCCCCCCCCCCC(=O)OC1CCCC1
Show InChI InChI=1S/C21H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-19-21(22)23-20-17-15-16-18-20/h20H,2-19H2,1H3
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.00E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAAA expressed in human HEK293 cells assessed as conversion of [1,2-14C]palmitoylethanolamine to [1,2-14C]ethanolamin...


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50171299
PNG
(CHEMBL190662 | Cyclohexanecarboxylic acid pentadec...)
Show SMILES CCCCCCCCCCCCCCCNC(=O)C1CCCCC1
Show InChI InChI=1S/C22H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-23-22(24)21-18-15-14-16-19-21/h21H,2-20H2,1H3,(H,23,24)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.70E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of human recombinant NAAA expressed in human HEK293 cells assessed as conversion of [1,2-14C]palmitoylethanolamine to [1,2-14C]ethanolamin...


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50171291
PNG
(CHEMBL139056 | Hexadecanoic acid cyclohexyl ester ...)
Show SMILES CCCCCCCCCCCCCCCC(=O)OC1CCCCC1
Show InChI InChI=1S/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-22(23)24-21-18-15-14-16-19-21/h21H,2-20H2,1H3
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.90E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of NAAA


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50171286
PNG
(3-Hydroxy-N-pentadecyl-propionamide | CHEMBL423904...)
Show SMILES CCCCCCCCCCCCCCCNC(=O)CCO
Show InChI InChI=1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-18(21)15-17-20/h20H,2-17H2,1H3,(H,19,21)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 3.20E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of NAAA


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase


(Homo sapiens (Human))
BDBM50171294
PNG
(CHEMBL138543 | HEXADECYLPROPIONATE | Propionic aci...)
Show SMILES CCCCCCCCCCCCCCCCOC(=O)CC
Show InChI InChI=1S/C19H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-19(20)4-2/h3-18H2,1-2H3
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 5.40E+4n/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Inhibition of NAAA


Bioorg Med Chem Lett 20: 1210-3 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.134
BindingDB Entry DOI: 10.7270/Q2319W1H
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%