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SMILES: Cc1ccccc1CNC(=O)COc1ccc(Cl)cc1C(=O)c1ccccc1

InChI Key: InChIKey=MSYIEAGYWMKNPR-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50470142   
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)
BDBM50470142
PNG
(CHEMBL46675)
Show SMILES Cc1ccccc1CNC(=O)COc1ccc(Cl)cc1C(=O)c1ccccc1
Show InChI InChI=1S/C23H20ClNO3/c1-16-7-5-6-10-18(16)14-25-22(26)15-28-21-12-11-19(24)13-20(21)23(27)17-8-3-2-4-9-17/h2-13H,14-15H2,1H3,(H,25,26)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.34E+3n/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