BDBM50484341 CHEMBL1835497

SMILES: Cc1cccc(Cc2cc(C)ccc2OCCn2ccc(=O)[nH]c2=O)c1

InChI Key: InChIKey=FEGLBNQXLJPNTP-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 = 50484341   

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)	BDBM50484341 (CHEMBL1835497) Show SMILES Cc1cccc(Cc2cc(C)ccc2OCCn2ccc(=O)[nH]c2=O)c1 Show InChI InChI=1S/C21H22N2O3/c1-15-4-3-5-17(12-15)14-18-13-16(2)6-7-19(18)26-11-10-23-9-8-20(24)22-21(23)25/h3-9,12-13H,10-11,14H2,1-2H3,(H,22,24,25)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	6.30E+3	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