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BDBM50350149 CHEMBL1814312

SMILES: COc1ccc(cc1CC=C)-c1cc(CC=C)cc(NC(C)=O)c1O

InChI Key: InChIKey=KNYQXFHNRYTONS-UHFFFAOYSA-N

Data: 1 KI  3 EC50

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 = 50350149   
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))
BDBM50350149
PNG
(CHEMBL1814312)
Show SMILES COc1ccc(cc1CC=C)-c1cc(CC=C)cc(NC(C)=O)c1O
Show InChI InChI=1S/C21H23NO3/c1-5-7-15-11-18(21(24)19(12-15)22-14(3)23)16-9-10-20(25-4)17(13-16)8-6-2/h5-6,9-13,24H,1-2,7-8H2,3-4H3,(H,22,23)
PDB

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



Universit£ di Pisa

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human CB2 receptor expressed in CHO cell membranes after 2 hrs


Eur J Med Chem 116: 252-266 (2016)


Article DOI: 10.1016/j.ejmech.2016.03.072
BindingDB Entry DOI: 10.7270/Q2DJ5HHP
More data for this
Ligand-Target Pair
GABA-A receptor; GABA-A site (alpha1/beta2 interface)


(Homo sapiens (Human))
BDBM50350149
PNG
(CHEMBL1814312)
Show SMILES COc1ccc(cc1CC=C)-c1cc(CC=C)cc(NC(C)=O)c1O
Show InChI InChI=1S/C21H23NO3/c1-5-7-15-11-18(21(24)19(12-15)22-14(3)23)16-9-10-20(25-4)17(13-16)8-6-2/h5-6,9-13,24H,1-2,7-8H2,3-4H3,(H,22,23)
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Article
PubMed
n/an/an/an/a 3.80E+3n/an/an/an/a



University of Vienna

Curated by ChEMBL


Assay Description
Modulation of GABA Aalpha1beta2 receptor expressed in Xenopus laevis oocytes assessed as potentiation of GABA-induced chloride current at holding pot...


J Med Chem 54: 5349-61 (2011)


Article DOI: 10.1021/jm200186n
BindingDB Entry DOI: 10.7270/Q2QR4XGP
More data for this
Ligand-Target Pair
GABA-A receptor; alpha-1/beta-2/gamma-2


(Homo sapiens (Human))
BDBM50350149
PNG
(CHEMBL1814312)
Show SMILES COc1ccc(cc1CC=C)-c1cc(CC=C)cc(NC(C)=O)c1O
Show InChI InChI=1S/C21H23NO3/c1-5-7-15-11-18(21(24)19(12-15)22-14(3)23)16-9-10-20(25-4)17(13-16)8-6-2/h5-6,9-13,24H,1-2,7-8H2,3-4H3,(H,22,23)
PDB

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PubMed
n/an/an/an/a 5.30E+3n/an/an/an/a



University of Graz

Curated by ChEMBL


Assay Description
Allosteric modulation of GABAAalpha1beta2gamma2s receptor (unknown origin) expressed in Xenopus laevis oocytes assessed as potentiation of GABA-induc...


Bioorg Med Chem 23: 6757-62 (2015)


BindingDB Entry DOI: 10.7270/Q2WQ05KM
More data for this
Ligand-Target Pair
GABA-A receptor; alpha-1/beta-2/gamma-2


(Homo sapiens (Human))
BDBM50350149
PNG
(CHEMBL1814312)
Show SMILES COc1ccc(cc1CC=C)-c1cc(CC=C)cc(NC(C)=O)c1O
Show InChI InChI=1S/C21H23NO3/c1-5-7-15-11-18(21(24)19(12-15)22-14(3)23)16-9-10-20(25-4)17(13-16)8-6-2/h5-6,9-13,24H,1-2,7-8H2,3-4H3,(H,22,23)
PDB

UniProtKB/SwissProt

antibodypedia
antibodypedia
antibodypedia
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CHEMBL
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PC sid
UniChem

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PubMed
n/an/an/an/a 6.81E+4n/an/an/an/a



University of Graz

Curated by ChEMBL


Assay Description
Partial agonist activity at GABAAalpha1beta2gamma2s receptor (unknown origin) expressed in Xenopus laevis oocytes assessed as induction of chloride c...


Bioorg Med Chem 23: 6757-62 (2015)


BindingDB Entry DOI: 10.7270/Q2WQ05KM
More data for this
Ligand-Target Pair