BDBM50332881 1-(2,4-Dichlorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-N-(5-hydroxypentyl)-4-methyl-1H-pyrazole-3-carboxamide::CHEMBL1631169

SMILES: Cc1ccc(C)n1-c1c(C)c(nn1-c1ccc(Cl)cc1Cl)C(=O)NCCCCCO

InChI Key: InChIKey=RRKHFMZRDDPEFW-UHFFFAOYSA-N

Data: 2 KI

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 2 hits for monomerid = 50332881   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50332881 (1-(2,4-Dichlorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1...) Show SMILES Cc1ccc(C)n1-c1c(C)c(nn1-c1ccc(Cl)cc1Cl)C(=O)NCCCCCO |(-3.67,-7.38,;-3.57,-8.93,;-4.76,-9.88,;-4.24,-11.31,;-2.7,-11.26,;-2.08,-12.19,;-2.28,-9.79,;-.87,-9.18,;-.32,-7.75,;-1.15,-6.44,;1.19,-7.82,;1.61,-9.29,;.34,-10.15,;.33,-11.7,;-1,-12.47,;-1,-14.01,;.34,-14.78,;.34,-16.32,;1.67,-14.01,;1.67,-12.46,;3.01,-11.68,;1.94,-6.45,;1.15,-5.15,;3.49,-6.42,;4.29,-7.73,;5.83,-7.68,;6.63,-9,;8.17,-8.96,;8.98,-10.28,;10.52,-10.24,)| Show InChI InChI=1S/C22H26Cl2N4O2/c1-14-7-8-15(2)27(14)22-16(3)20(21(30)25-11-5-4-6-12-29)26-28(22)19-10-9-17(23)13-18(19)24/h7-10,13,29H,4-6,11-12H2,1-3H3,(H,25,30)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	372	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sapienza Universit£ di Roma Curated by ChEMBL					Assay Description Displacement of [3H]CP-55,940 from recombinant human CB1 receptor transfected in HEK cells				Eur J Med Chem 45: 5878-86 (2010) Article DOI: 10.1016/j.ejmech.2010.09.053 BindingDB Entry DOI: 10.7270/Q22Z15T3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50332881 (1-(2,4-Dichlorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1...) Show SMILES Cc1ccc(C)n1-c1c(C)c(nn1-c1ccc(Cl)cc1Cl)C(=O)NCCCCCO |(-3.67,-7.38,;-3.57,-8.93,;-4.76,-9.88,;-4.24,-11.31,;-2.7,-11.26,;-2.08,-12.19,;-2.28,-9.79,;-.87,-9.18,;-.32,-7.75,;-1.15,-6.44,;1.19,-7.82,;1.61,-9.29,;.34,-10.15,;.33,-11.7,;-1,-12.47,;-1,-14.01,;.34,-14.78,;.34,-16.32,;1.67,-14.01,;1.67,-12.46,;3.01,-11.68,;1.94,-6.45,;1.15,-5.15,;3.49,-6.42,;4.29,-7.73,;5.83,-7.68,;6.63,-9,;8.17,-8.96,;8.98,-10.28,;10.52,-10.24,)| Show InChI InChI=1S/C22H26Cl2N4O2/c1-14-7-8-15(2)27(14)22-16(3)20(21(30)25-11-5-4-6-12-29)26-28(22)19-10-9-17(23)13-18(19)24/h7-10,13,29H,4-6,11-12H2,1-3H3,(H,25,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Sapienza Universit£ di Roma Curated by ChEMBL					Assay Description Displacement of [3H]CP-55,940 from recombinant human CB2 receptor transfected in HEK cells				Eur J Med Chem 45: 5878-86 (2010) Article DOI: 10.1016/j.ejmech.2010.09.053 BindingDB Entry DOI: 10.7270/Q22Z15T3
					More data for this Ligand-Target Pair