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SMILES: OC(c1ccnc(Nc2ccc(cc2)C#N)n1)c1ccccc1Cl

InChI Key: InChIKey=XQMJLGLPGJBACD-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50485192   
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


(Human immunodeficiency virus 1)		BDBM50485192
PNG
(CHEMBL1817673)
Show SMILES OC(c1ccnc(Nc2ccc(cc2)C#N)n1)c1ccccc1Cl
Show InChI InChI=1S/C18H13ClN4O/c19-15-4-2-1-3-14(15)17(24)16-9-10-21-18(23-16)22-13-7-5-12(11-20)6-8-13/h1-10,17,24H,(H,21,22,23)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 450n/an/an/an/an/an/a



Fudan University

Curated by ChEMBL


Assay Description
Inhibition of HIV1 wildtype reverse transcriptase using poly(rA)/oligo(dT)15 as template by colometric streptavidin alkaline phosphate reporter assay

Eur J Med Chem 53: 229-34 (2012)


Article DOI: 10.1016/j.ejmech.2012.04.004
BindingDB Entry DOI: 10.7270/Q2KK9FN2
More data for this
Ligand-Target Pair