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SMILES: CC(C)(C)c1cc(NC(=O)N2CCCN(CC2)C(=O)C2CCOCC2)[nH]n1

InChI Key: InChIKey=VEKIZUXKGBGSGF-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50340997   
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 1


(Homo sapiens (Human))
BDBM50340997
PNG
(CHEMBL1762416 | N-(3-tert-butyl-1H-pyrazol-5-yl)-4...)
Show SMILES CC(C)(C)c1cc(NC(=O)N2CCCN(CC2)C(=O)C2CCOCC2)[nH]n1
Show InChI InChI=1S/C19H31N5O3/c1-19(2,3)15-13-16(22-21-15)20-18(26)24-8-4-7-23(9-10-24)17(25)14-5-11-27-12-6-14/h13-14H,4-12H2,1-3H3,(H2,20,21,22,26)
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Article
PubMed
n/an/an/an/a>2.00E+4n/an/an/an/a



Boehringer Ingelheim Pharmaceuticals

Curated by ChEMBL


Assay Description
Agonist activity at human CB1 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated cAMP production


Bioorg Med Chem Lett 21: 2011-6 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.017
BindingDB Entry DOI: 10.7270/Q2KK9C2M
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50340997
PNG
(CHEMBL1762416 | N-(3-tert-butyl-1H-pyrazol-5-yl)-4...)
Show SMILES CC(C)(C)c1cc(NC(=O)N2CCCN(CC2)C(=O)C2CCOCC2)[nH]n1
Show InChI InChI=1S/C19H31N5O3/c1-19(2,3)15-13-16(22-21-15)20-18(26)24-8-4-7-23(9-10-24)17(25)14-5-11-27-12-6-14/h13-14H,4-12H2,1-3H3,(H2,20,21,22,26)
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DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 1.32E+4n/an/an/an/a



Boehringer Ingelheim Pharmaceuticals

Curated by ChEMBL


Assay Description
Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated cAMP production


Bioorg Med Chem Lett 21: 2011-6 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.017
BindingDB Entry DOI: 10.7270/Q2KK9C2M
More data for this
Ligand-Target Pair