BDBM50341153 4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)phenol::CHEMBL1760714

SMILES: Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12

InChI Key: InChIKey=GAZUTEYOOWJEAA-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50341153   

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
Monoamine Oxidase Type B (MAO-B) (Rattus norvegicus (rat))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.75	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.51	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase (flavin-containing) A (Homo sapiens (Human))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	225	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Monoamine oxidase (Rattus norvegicus (rat))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	385	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair