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SMILES: CN1CCN(CC1)c1nccc2[nH]c(cc12)-c1nc(CCc2ccc(Cl)cc2)no1

InChI Key: InChIKey=JLFKBORRFRIWDY-UHFFFAOYSA-N

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50185537   
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
Nociceptin receptor


(Homo sapiens (Human))
BDBM50185537
PNG
(2-(3-(4-chlorophenethyl)-1,2,4-oxadiazol-5-yl)-4-(...)
Show SMILES CN1CCN(CC1)c1nccc2[nH]c(cc12)-c1nc(CCc2ccc(Cl)cc2)no1
Show InChI InChI=1S/C22H23ClN6O/c1-28-10-12-29(13-11-28)21-17-14-19(25-18(17)8-9-24-21)22-26-20(27-30-22)7-4-15-2-5-16(23)6-3-15/h2-3,5-6,8-9,14,25H,4,7,10-13H2,1H3
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PC cid
PC sid
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Similars

Article
PubMed
n/an/a 40n/an/an/an/an/an/a



Banyu Tsukuba Research Institute

Curated by ChEMBL


Assay Description
Displacement of [125I][Tyr14]N/OFQ from ORL1 receptor transfected in CHO cells


Bioorg Med Chem Lett 16: 3569-73 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.086
BindingDB Entry DOI: 10.7270/Q2N879D1
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))
BDBM50185537
PNG
(2-(3-(4-chlorophenethyl)-1,2,4-oxadiazol-5-yl)-4-(...)
Show SMILES CN1CCN(CC1)c1nccc2[nH]c(cc12)-c1nc(CCc2ccc(Cl)cc2)no1
Show InChI InChI=1S/C22H23ClN6O/c1-28-10-12-29(13-11-28)21-17-14-19(25-18(17)8-9-24-21)22-26-20(27-30-22)7-4-15-2-5-16(23)6-3-15/h2-3,5-6,8-9,14,25H,4,7,10-13H2,1H3
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 199n/an/an/an/an/an/a



Banyu Tsukuba Research Institute

Curated by ChEMBL


Assay Description
Antagonist activity against ORL1 receptor by GTPgammaS assay


Bioorg Med Chem Lett 16: 3569-73 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.086
BindingDB Entry DOI: 10.7270/Q2N879D1
More data for this
Ligand-Target Pair