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BDBM50244288 CHEMBL4076334

SMILES: CCOc1ccc(Cc2nc3cc(ccc3n2CCC(C)C)C(=O)Nc2ccccc2)cc1

InChI Key: InChIKey=UYOHDNVAVCHIJW-UHFFFAOYSA-N

Data: 1 KI  3 IC50

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 4 hits for monomerid = 50244288   
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
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50244288
PNG
(CHEMBL4076334)
Show SMILES CCOc1ccc(Cc2nc3cc(ccc3n2CCC(C)C)C(=O)Nc2ccccc2)cc1
Show InChI InChI=1S/C28H31N3O2/c1-4-33-24-13-10-21(11-14-24)18-27-30-25-19-22(28(32)29-23-8-6-5-7-9-23)12-15-26(25)31(27)17-16-20(2)3/h5-15,19-20H,4,16-18H2,1-3H3,(H,29,32)
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Article
PubMed
1.44E+4n/an/an/an/an/an/an/an/a



Julius Maximilian University of W£rzburg

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55950 from human CB2 receptor expressed in HEK cell membranes after 3 hrs by scintillation counting method


J Med Chem 61: 1646-1663 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01760
BindingDB Entry DOI: 10.7270/Q2RJ4MWK
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50244288
PNG
(CHEMBL4076334)
Show SMILES CCOc1ccc(Cc2nc3cc(ccc3n2CCC(C)C)C(=O)Nc2ccccc2)cc1
Show InChI InChI=1S/C28H31N3O2/c1-4-33-24-13-10-21(11-14-24)18-27-30-25-19-22(28(32)29-23-8-6-5-7-9-23)12-15-26(25)31(27)17-16-20(2)3/h5-15,19-20H,4,16-18H2,1-3H3,(H,29,32)
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Article
PubMed
n/an/a 1.58E+4n/an/an/an/an/an/a



Julius Maximilian University of W£rzburg

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55950 from human CB2 receptor expressed in HEK cell membranes after 3 hrs by scintillation counting method


J Med Chem 61: 1646-1663 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01760
BindingDB Entry DOI: 10.7270/Q2RJ4MWK
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50244288
PNG
(CHEMBL4076334)
Show SMILES CCOc1ccc(Cc2nc3cc(ccc3n2CCC(C)C)C(=O)Nc2ccccc2)cc1
Show InChI InChI=1S/C28H31N3O2/c1-4-33-24-13-10-21(11-14-24)18-27-30-25-19-22(28(32)29-23-8-6-5-7-9-23)12-15-26(25)31(27)17-16-20(2)3/h5-15,19-20H,4,16-18H2,1-3H3,(H,29,32)
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PubMed
n/an/a 1.26E+3n/an/an/an/an/an/a



Julius Maximilian University of W£rzburg

Curated by ChEMBL


Assay Description
Inhibition of human BChE using BTC iodide as substrate preincubated for 4.5 mins followed by substrate addition measured after 2.5 mins by Ellman's m...


J Med Chem 61: 1646-1663 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01760
BindingDB Entry DOI: 10.7270/Q2RJ4MWK
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50244288
PNG
(CHEMBL4076334)
Show SMILES CCOc1ccc(Cc2nc3cc(ccc3n2CCC(C)C)C(=O)Nc2ccccc2)cc1
Show InChI InChI=1S/C28H31N3O2/c1-4-33-24-13-10-21(11-14-24)18-27-30-25-19-22(28(32)29-23-8-6-5-7-9-23)12-15-26(25)31(27)17-16-20(2)3/h5-15,19-20H,4,16-18H2,1-3H3,(H,29,32)
PDB
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Article
PubMed
n/an/a 1.20E+3n/an/an/an/an/an/a



Julius Maximilian University of W£rzburg

Curated by ChEMBL


Assay Description
Inhibition of human BChE using BTC iodide as substrate preincubated for 4.5 mins followed by substrate addition measured after 2.5 mins by Ellman's m...


J Med Chem 61: 1646-1663 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01760
BindingDB Entry DOI: 10.7270/Q2RJ4MWK
More data for this
Ligand-Target Pair