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SMILES: Clc1ccc(OCC(=O)c2cc3ccccc3[nH]2)c(c1)C(=O)c1ccccc1

InChI Key: InChIKey=UJCPFIBGORBIRP-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50470146   
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)		BDBM50470146
PNG
(CHEMBL417183)
Show SMILES Clc1ccc(OCC(=O)c2cc3ccccc3[nH]2)c(c1)C(=O)c1ccccc1
Show InChI InChI=1S/C23H16ClNO3/c24-17-10-11-22(18(13-17)23(27)15-6-2-1-3-7-15)28-14-21(26)20-12-16-8-4-5-9-19(16)25-20/h1-13,25H,14H2
PDB
MMDB

UniProtKB/TrEMBL

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 161n/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