BDBM50484336 CHEMBL1835498

SMILES: Cc1ccc(OCCn2ccc(=O)[nH]c2=O)c(Cc2cc(C)cc(C)c2)c1

InChI Key: InChIKey=MBTRIESVTFCYJW-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 = 50484336   

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)	BDBM50484336 (CHEMBL1835498) Show SMILES Cc1ccc(OCCn2ccc(=O)[nH]c2=O)c(Cc2cc(C)cc(C)c2)c1 Show InChI InChI=1S/C22H24N2O3/c1-15-4-5-20(27-9-8-24-7-6-21(25)23-22(24)26)19(13-15)14-18-11-16(2)10-17(3)12-18/h4-7,10-13H,8-9,14H2,1-3H3,(H,23,25,26)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.70E+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