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SMILES: Clc1ccccc1NC(=O)Nc1ccc(cc1)-c1ccnc2nc[nH]c12

InChI Key: InChIKey=OUJNTZAPROXXHI-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50364627   

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 3A5 (Homo sapiens (Human))	BDBM50364627 (CHEMBL1951322) Show SMILES Clc1ccccc1NC(=O)Nc1ccc(cc1)-c1ccnc2nc[nH]c12 Show InChI InChI=1S/C19H14ClN5O/c20-15-3-1-2-4-16(15)25-19(26)24-13-7-5-12(6-8-13)14-9-10-21-18-17(14)22-11-23-18/h1-11H,(H,21,22,23)(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of recombinant human CYP3A5 in supersomes using midazolam as substrate after 5 mins by LC-MS/MS analysis				Bioorg Med Chem Lett 22: 1611-4 (2012) Article DOI: 10.1016/j.bmcl.2011.12.125 BindingDB Entry DOI: 10.7270/Q2T72HXJ
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50364627 (CHEMBL1951322) Show SMILES Clc1ccccc1NC(=O)Nc1ccc(cc1)-c1ccnc2nc[nH]c12 Show InChI InChI=1S/C19H14ClN5O/c20-15-3-1-2-4-16(15)25-19(26)24-13-7-5-12(6-8-13)14-9-10-21-18-17(14)22-11-23-18/h1-11H,(H,21,22,23)(H2,24,25,26)	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	600	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of recombinant human CYP3A4 in supersomes using midazolam as substrate after 5 mins by LC-MS/MS analysis				Bioorg Med Chem Lett 22: 1611-4 (2012) Article DOI: 10.1016/j.bmcl.2011.12.125 BindingDB Entry DOI: 10.7270/Q2T72HXJ
					More data for this Ligand-Target Pair