BDBM50484335 CHEMBL1835513

SMILES: Cc1cc(C)cc(c1)C(=O)c1cc(Cl)ccc1OCCCn1ccc(=O)[nH]c1=O

InChI Key: InChIKey=ASRCBSXZUKIXQH-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 = 50484335   

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)	BDBM50484335 (CHEMBL1835513) Show SMILES Cc1cc(C)cc(c1)C(=O)c1cc(Cl)ccc1OCCCn1ccc(=O)[nH]c1=O Show InChI InChI=1S/C22H21ClN2O4/c1-14-10-15(2)12-16(11-14)21(27)18-13-17(23)4-5-19(18)29-9-3-7-25-8-6-20(26)24-22(25)28/h4-6,8,10-13H,3,7,9H2,1-2H3,(H,24,26,28)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>2.42E+5	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