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BDBM50232930 CHEMBL4067246

SMILES: [H][C@@]12CC[C@@](C)(C1)[C@H](NC(=O)c1cc(nn(Cc3ccc(F)cc3)c1=O)-c1ccc(Cl)c(C)c1)C2(C)C

InChI Key: InChIKey=BYGBMSYENNXFDF-LEFTWQHSSA-N

Data: 2 KI  1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50232930   
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))
BDBM50232930
PNG
(CHEMBL4067246)
Show SMILES [H][C@@]12CC[C@@](C)(C1)[C@H](NC(=O)c1cc(nn(Cc3ccc(F)cc3)c1=O)-c1ccc(Cl)c(C)c1)C2(C)C |r|
Show InChI InChI=1S/C29H31ClFN3O2/c1-17-13-19(7-10-23(17)30)24-14-22(26(36)34(33-24)16-18-5-8-21(31)9-6-18)25(35)32-27-28(2,3)20-11-12-29(27,4)15-20/h5-10,13-14,20,27H,11-12,15-16H2,1-4H3,(H,32,35)/t20-,27-,29+/m1/s1
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PubMed
2.60n/an/an/an/an/an/an/an/a



University of Sassari

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human CB2 receptor expressed in HEK293 EBNA cell membranes after 90 mins by liquid scintillation and luminescence co...


Eur J Med Chem 127: 398-412 (2017)


BindingDB Entry DOI: 10.7270/Q26W9D9V
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50232930
PNG
(CHEMBL4067246)
Show SMILES [H][C@@]12CC[C@@](C)(C1)[C@H](NC(=O)c1cc(nn(Cc3ccc(F)cc3)c1=O)-c1ccc(Cl)c(C)c1)C2(C)C |r|
Show InChI InChI=1S/C29H31ClFN3O2/c1-17-13-19(7-10-23(17)30)24-14-22(26(36)34(33-24)16-18-5-8-21(31)9-6-18)25(35)32-27-28(2,3)20-11-12-29(27,4)15-20/h5-10,13-14,20,27H,11-12,15-16H2,1-4H3,(H,32,35)/t20-,27-,29+/m1/s1
PDB

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PC sid
UniChem

Similars

PubMed
>4.00E+3n/an/an/an/an/an/an/an/a



University of Sassari

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human CB1 receptor expressed in HEK293 EBNA cell membranes after 90 mins by liquid scintillation and luminescence co...


Eur J Med Chem 127: 398-412 (2017)


BindingDB Entry DOI: 10.7270/Q26W9D9V
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50232930
PNG
(CHEMBL4067246)
Show SMILES [H][C@@]12CC[C@@](C)(C1)[C@H](NC(=O)c1cc(nn(Cc3ccc(F)cc3)c1=O)-c1ccc(Cl)c(C)c1)C2(C)C |r|
Show InChI InChI=1S/C29H31ClFN3O2/c1-17-13-19(7-10-23(17)30)24-14-22(26(36)34(33-24)16-18-5-8-21(31)9-6-18)25(35)32-27-28(2,3)20-11-12-29(27,4)15-20/h5-10,13-14,20,27H,11-12,15-16H2,1-4H3,(H,32,35)/t20-,27-,29+/m1/s1
PDB

Reactome pathway
KEGG

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UniProtKB/TrEMBL

DrugBank
antibodypedia
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PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 51n/an/an/an/an/an/a



University of Sassari

Curated by ChEMBL


Assay Description
Inverse agonist activity at human CB2 receptor expressed in HEK293 EBNA cell membranes after 30 mins by [35S]-GTPgammaS binding assay


Eur J Med Chem 127: 398-412 (2017)


BindingDB Entry DOI: 10.7270/Q26W9D9V
More data for this
Ligand-Target Pair