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Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Cannabinoid receptor 2' and Ligand = 'BDBM50156022'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50156022
PNG
(CHEMBL3780166)
Show SMILES CCCCCn1c2ccccc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:25:24:27:21.20.19,25:20:27:24.26.23,THB:23:24:21.22.27:19,23:22:19:24.26.25|
Show InChI InChI=1S/C30H37NO10S/c1-14(33)37-25-21(13-32)40-29(27(39-16(3)35)26(25)38-15(2)34)42-22-9-7-18-19-12-17-6-8-20(36-5)24-23(17)30(18,28(22)41-24)10-11-31(19)4/h6-9,18-19,21-22,25-29,32H,10-13H2,1-5H3/t18-,19+,21?,22?,25?,26?,27?,28-,29?,30-/m0/s1
PDB

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PC cid
PC sid
UniChem
PubMed
0.970n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Siena

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP-55940 from human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by Competition binding assay


J Med Chem 59: 1052-67 (2016)

More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50156022
PNG
(CHEMBL3780166)
Show SMILES CCCCCn1c2ccccc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:25:24:27:21.20.19,25:20:27:24.26.23,THB:23:24:21.22.27:19,23:22:19:24.26.25|
Show InChI InChI=1S/C30H37NO10S/c1-14(33)37-25-21(13-32)40-29(27(39-16(3)35)26(25)38-15(2)34)42-22-9-7-18-19-12-17-6-8-20(36-5)24-23(17)30(18,28(22)41-24)10-11-31(19)4/h6-9,18-19,21-22,25-29,32H,10-13H2,1-5H3/t18-,19+,21?,22?,25?,26?,27?,28-,29?,30-/m0/s1
PDB

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UniProtKB/SwissProt

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antibodypedia
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CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/a 2n/an/an/an/an/an/a



Universit£ degli Studi di Siena

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP-55940 from human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by Competition binding assay


J Med Chem 59: 1052-67 (2016)

More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50156022
PNG
(CHEMBL3780166)
Show SMILES CCCCCn1c2ccccc2c(O)c(C(=O)NC23CC4CC(CC(C4)C2)C3)c1=O |TLB:25:24:27:21.20.19,25:20:27:24.26.23,THB:23:24:21.22.27:19,23:22:19:24.26.25|
Show InChI InChI=1S/C30H37NO10S/c1-14(33)37-25-21(13-32)40-29(27(39-16(3)35)26(25)38-15(2)34)42-22-9-7-18-19-12-17-6-8-20(36-5)24-23(17)30(18,28(22)41-24)10-11-31(19)4/h6-9,18-19,21-22,25-29,32H,10-13H2,1-5H3/t18-,19+,21?,22?,25?,26?,27?,28-,29?,30-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/an/an/a 2.40n/an/an/an/a



Universit£ degli Studi di Siena

Curated by ChEMBL


Assay Description
Inverse agonist activity at recombinant human CB2 receptor expressed in CHO-K1 cells assessed as increase in NHK477-induced cAMP production by lumine...


J Med Chem 59: 1052-67 (2016)

More data for this
Ligand-Target Pair