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SMILES: Clc1cc(OCC(=O)Nc2ccccc2)c(cc1Cl)C(=O)c1ccccc1

InChI Key: InChIKey=BKFKCWWZKWVGKL-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50470145   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
Reverse transcriptase/RNaseH


(Human immunodeficiency virus 1)		BDBM50470145
PNG
(CHEMBL46925)
Show SMILES Clc1cc(OCC(=O)Nc2ccccc2)c(cc1Cl)C(=O)c1ccccc1
Show InChI InChI=1S/C21H15Cl2NO3/c22-17-11-16(21(26)14-7-3-1-4-8-14)19(12-18(17)23)27-13-20(25)24-15-9-5-2-6-10-15/h1-12H,13H2,(H,24,25)
PDB
MMDB

UniProtKB/TrEMBL

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 35n/an/an/an/an/an/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