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SMILES: Clc1ccc(OCC(=O)Nc2ccccc2)c(C(=O)c2ccccc2)c1Cl

InChI Key: InChIKey=IEQJYVOWNXVHRZ-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50470167   
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)
BDBM50470167
PNG
(CHEMBL44845)
Show SMILES Clc1ccc(OCC(=O)Nc2ccccc2)c(C(=O)c2ccccc2)c1Cl
Show InChI InChI=1S/C21H15Cl2NO3/c22-16-11-12-17(27-13-18(25)24-15-9-5-2-6-10-15)19(20(16)23)21(26)14-7-3-1-4-8-14/h1-12H,13H2,(H,24,25)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>2.49E+5n/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