BDBM50470166 CHEMBL44002

SMILES: Clc1ccc(OCc2nc3ccccc3[nH]2)c(c1)C(=O)c1ccccc1

InChI Key: InChIKey=XGIUYZNNEVXMAS-UHFFFAOYSA-N

Data: 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 1 hit for monomerid = 50470166   

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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50470166 (CHEMBL44002) Show SMILES Clc1ccc(OCc2nc3ccccc3[nH]2)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C21H15ClN2O2/c22-15-10-11-19(16(12-15)21(25)14-6-2-1-3-7-14)26-13-20-23-17-8-4-5-9-18(17)24-20/h1-12H,13H2,(H,23,24)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Research and Development Limited Curated by ChEMBL					Assay Description Inhibitory activity against HIV-1 reverse transcriptase				J Med Chem 38: 1657-65 (1995) Article DOI: 10.1021/jm00010a010 BindingDB Entry DOI: 10.7270/Q27947DP
					More data for this Ligand-Target Pair