null

SMILES: C[C@H]1CN(Cc2ccc(cc2)-c2ccccc2C(=O)N2CCC(CC2)Nc2ccc(Cl)cc2)C[C@@H](C)N1

InChI Key: InChIKey=UCGDJSGANNJRLB-ZRZAMGCNSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50254971   

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
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50254971 (CHEMBL481575 | [4-(4-Chloro-phenylamino)-piperidin...) Show SMILES C[C@H]1CN(Cc2ccc(cc2)-c2ccccc2C(=O)N2CCC(CC2)Nc2ccc(Cl)cc2)C[C@@H](C)N1 |r| Show InChI InChI=1S/C31H37ClN4O/c1-22-19-35(20-23(2)33-22)21-24-7-9-25(10-8-24)29-5-3-4-6-30(29)31(37)36-17-15-28(16-18-36)34-27-13-11-26(32)12-14-27/h3-14,22-23,28,33-34H,15-21H2,1-2H3/t22-,23+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Inhibition of CYP3A4 (unknown origin) using diethoxyfluorescein substrate				Bioorg Med Chem Lett 18: 6429-36 (2008) Article DOI: 10.1016/j.bmcl.2008.10.072 BindingDB Entry DOI: 10.7270/Q2HQ3ZR3
					More data for this Ligand-Target Pair
Motilin receptor (Homo sapiens (Human))	BDBM50254971 (CHEMBL481575 | [4-(4-Chloro-phenylamino)-piperidin...) Show SMILES C[C@H]1CN(Cc2ccc(cc2)-c2ccccc2C(=O)N2CCC(CC2)Nc2ccc(Cl)cc2)C[C@@H](C)N1 |r| Show InChI InChI=1S/C31H37ClN4O/c1-22-19-35(20-23(2)33-22)21-24-7-9-25(10-8-24)29-5-3-4-6-30(29)31(37)36-17-15-28(16-18-36)34-27-13-11-26(32)12-14-27/h3-14,22-23,28,33-34H,15-21H2,1-2H3/t22-,23+	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	50.1	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Agonist activity at human recombinant motilin receptor expressed in HEK293 cells by FLIPR assay				Bioorg Med Chem Lett 18: 6429-36 (2008) Article DOI: 10.1016/j.bmcl.2008.10.072 BindingDB Entry DOI: 10.7270/Q2HQ3ZR3
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50254971 (CHEMBL481575 | [4-(4-Chloro-phenylamino)-piperidin...) Show SMILES C[C@H]1CN(Cc2ccc(cc2)-c2ccccc2C(=O)N2CCC(CC2)Nc2ccc(Cl)cc2)C[C@@H](C)N1 |r| Show InChI InChI=1S/C31H37ClN4O/c1-22-19-35(20-23(2)33-22)21-24-7-9-25(10-8-24)29-5-3-4-6-30(29)31(37)36-17-15-28(16-18-36)34-27-13-11-26(32)12-14-27/h3-14,22-23,28,33-34H,15-21H2,1-2H3/t22-,23+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Inhibition of CYP3A4 (unknown origin) using phenylpiperazinylmethylbenzylresofurin substrate				Bioorg Med Chem Lett 18: 6429-36 (2008) Article DOI: 10.1016/j.bmcl.2008.10.072 BindingDB Entry DOI: 10.7270/Q2HQ3ZR3
					More data for this Ligand-Target Pair