BDBM50484328 CHEMBL1835503

SMILES: Clc1ccc(OCCn2ccc(=O)[nH]c2=O)c(c1)C(=O)c1ccccc1

InChI Key: InChIKey=NEWMBJKXVYZMIX-UHFFFAOYSA-N

Data: 1 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 1 hit for monomerid = 50484328   

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 (Human immunodeficiency virus 1)	BDBM50484328 (CHEMBL1835503) Show SMILES Clc1ccc(OCCn2ccc(=O)[nH]c2=O)c(c1)C(=O)c1ccccc1 Show InChI InChI=1S/C19H15ClN2O4/c20-14-6-7-16(15(12-14)18(24)13-4-2-1-3-5-13)26-11-10-22-9-8-17(23)21-19(22)25/h1-9,12H,10-11H2,(H,21,23,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	650	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Volgograd State Medical University Curated by ChEMBL					Assay Description Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...				Bioorg Med Chem 19: 5794-802 (2011) Article DOI: 10.1016/j.bmc.2011.08.025 BindingDB Entry DOI: 10.7270/Q2057JRG
					More data for this Ligand-Target Pair