BDBM50196110 CHEMBL217665::GNF-PF-2857::N-(4-(4-methylpiperazin-1-yl)phenyl)quinolin-4-amine::[4-(4-methylpiperazin-1-yl)phenyl]quinolin-4-ylamine

SMILES: CN1CCN(CC1)c1ccc(Nc2ccnc3ccccc23)cc1

InChI Key: InChIKey=RXXDJBWYJTWSKV-UHFFFAOYSA-N

Data: 4 KI  1 IC50

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 5 hits for monomerid = 50196110   

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
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50196110 (CHEMBL217665 | GNF-PF-2857 | N-(4-(4-methylpiperaz...) Show SMILES CN1CCN(CC1)c1ccc(Nc2ccnc3ccccc23)cc1 Show InChI InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	720	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Juvantia Pharma Ltd Curated by ChEMBL					Assay Description Displacement of [3H]rauwolscine from human ADRA2A expressed in S115 cells				J Med Chem 49: 6351-63 (2006) Article DOI: 10.1021/jm060262x BindingDB Entry DOI: 10.7270/Q2RB747B
					More data for this Ligand-Target Pair
Alpha-2C adrenergic receptor (Homo sapiens (Human))	BDBM50196110 (CHEMBL217665 | GNF-PF-2857 | N-(4-(4-methylpiperaz...) Show SMILES CN1CCN(CC1)c1ccc(Nc2ccnc3ccccc23)cc1 Show InChI InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Chemistry Timisoara of the Romanian Academy Curated by ChEMBL					Assay Description Binding affinity to human cloned Alpha-2C adrenergic receptor				Eur J Med Chem 46: 877-84 (2011) Article DOI: 10.1016/j.ejmech.2010.12.026 BindingDB Entry DOI: 10.7270/Q2474C44
					More data for this Ligand-Target Pair
Alpha-2C adrenergic receptor (Homo sapiens (Human))	BDBM50196110 (CHEMBL217665 | GNF-PF-2857 | N-(4-(4-methylpiperaz...) Show SMILES CN1CCN(CC1)c1ccc(Nc2ccnc3ccccc23)cc1 Show InChI InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Juvantia Pharma Ltd Curated by ChEMBL					Assay Description Displacement of [3H]rauwolscine from human ADRA2C expressed in S115 cells				J Med Chem 49: 6351-63 (2006) Article DOI: 10.1021/jm060262x BindingDB Entry DOI: 10.7270/Q2RB747B
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (Homo sapiens (Human))	BDBM50196110 (CHEMBL217665 | GNF-PF-2857 | N-(4-(4-methylpiperaz...) Show SMILES CN1CCN(CC1)c1ccc(Nc2ccnc3ccccc23)cc1 Show InChI InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Juvantia Pharma Ltd Curated by ChEMBL					Assay Description Displacement of [3H]rauwolscine from human ADRA2B expressed in S115 cells				J Med Chem 49: 6351-63 (2006) Article DOI: 10.1021/jm060262x BindingDB Entry DOI: 10.7270/Q2RB747B
					More data for this Ligand-Target Pair
MAP kinase-activated protein kinase 2 (Homo sapiens (Human))	BDBM50196110 (CHEMBL217665 | GNF-PF-2857 | N-(4-(4-methylpiperaz...) Show SMILES CN1CCN(CC1)c1ccc(Nc2ccnc3ccccc23)cc1 Show InChI InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca R&D Lund Curated by ChEMBL					Assay Description Inhibition of MK2 assessed as inhibition of [33P]ATP incorporation in to substrate after 30 mins by scintillation counting				Bioorg Med Chem Lett 20: 4738-40 (2010) Article DOI: 10.1016/j.bmcl.2010.06.107 BindingDB Entry DOI: 10.7270/Q2HX1CVQ
					More data for this Ligand-Target Pair