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BDBM50253528 5-(5-(Cyclohexylethynyl)thiophen-2-yl)-1-(2,4-dichlorophenyl)-N-(hexahydrocyclopenta[c]pyrrol-2(1H)-yl)-4-methyl-1H-pyrazole-3-carboxamide::CHEMBL524158

SMILES: Cc1c(nn(c1-c1ccc(s1)C#CC1CCCCC1)-c1ccc(Cl)cc1Cl)C(=O)NN1CC2CCCC2C1

InChI Key: InChIKey=UVLAMOAOUZDNJJ-UHFFFAOYSA-N

Data: 2 IC50  1 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 3 hits for monomerid = 50253528   
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))
BDBM50253528
PNG
(5-(5-(Cyclohexylethynyl)thiophen-2-yl)-1-(2,4-dich...)
Show SMILES Cc1c(nn(c1-c1ccc(s1)C#CC1CCCCC1)-c1ccc(Cl)cc1Cl)C(=O)NN1CC2CCCC2C1
Show InChI InChI=1S/C30H32Cl2N4OS/c1-19-28(30(37)34-35-17-21-8-5-9-22(21)18-35)33-36(26-14-11-23(31)16-25(26)32)29(19)27-15-13-24(38-27)12-10-20-6-3-2-4-7-20/h11,13-16,20-22H,2-9,17-18H2,1H3,(H,34,37)
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Article
PubMed
n/an/a 1.73E+3n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human CB2 receptor expressed in HEK293 cells


J Med Chem 51: 5397-412 (2008)


Article DOI: 10.1021/jm800066v
BindingDB Entry DOI: 10.7270/Q24M94BM
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50253528
PNG
(5-(5-(Cyclohexylethynyl)thiophen-2-yl)-1-(2,4-dich...)
Show SMILES Cc1c(nn(c1-c1ccc(s1)C#CC1CCCCC1)-c1ccc(Cl)cc1Cl)C(=O)NN1CC2CCCC2C1
Show InChI InChI=1S/C30H32Cl2N4OS/c1-19-28(30(37)34-35-17-21-8-5-9-22(21)18-35)33-36(26-14-11-23(31)16-25(26)32)29(19)27-15-13-24(38-27)12-10-20-6-3-2-4-7-20/h11,13-16,20-22H,2-9,17-18H2,1H3,(H,34,37)
PDB

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Article
PubMed
n/an/an/an/a 294n/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Antagonist activity at human CB1 receptor expressed in HEK293 cells assessed as inhibition of Eu-GTP binding


J Med Chem 51: 5397-412 (2008)


Article DOI: 10.1021/jm800066v
BindingDB Entry DOI: 10.7270/Q24M94BM
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50253528
PNG
(5-(5-(Cyclohexylethynyl)thiophen-2-yl)-1-(2,4-dich...)
Show SMILES Cc1c(nn(c1-c1ccc(s1)C#CC1CCCCC1)-c1ccc(Cl)cc1Cl)C(=O)NN1CC2CCCC2C1
Show InChI InChI=1S/C30H32Cl2N4OS/c1-19-28(30(37)34-35-17-21-8-5-9-22(21)18-35)33-36(26-14-11-23(31)16-25(26)32)29(19)27-15-13-24(38-27)12-10-20-6-3-2-4-7-20/h11,13-16,20-22H,2-9,17-18H2,1H3,(H,34,37)
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 7.80n/an/an/an/an/an/a



National Health Research Institutes

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human CB1 receptor expressed in HEK293 cells


J Med Chem 51: 5397-412 (2008)


Article DOI: 10.1021/jm800066v
BindingDB Entry DOI: 10.7270/Q24M94BM
More data for this
Ligand-Target Pair