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BDBM50492333 CHEMBL2402856

SMILES: N#Cc1ccc(Nc2nccc(Oc3ccc(OCc4ccccc4)cc3)n2)cc1

InChI Key: InChIKey=SKQUAEBSRKYGMF-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50492333   
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)
BDBM50492333
PNG
(CHEMBL2402856)
Show SMILES N#Cc1ccc(Nc2nccc(Oc3ccc(OCc4ccccc4)cc3)n2)cc1
Show InChI InChI=1S/C24H18N4O2/c25-16-18-6-8-20(9-7-18)27-24-26-15-14-23(28-24)30-22-12-10-21(11-13-22)29-17-19-4-2-1-3-5-19/h1-15H,17H2,(H,26,27,28)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 3.10E+4n/an/an/an/an/an/a



Fudan University

Curated by ChEMBL


Assay Description
Inhibition of recombinant wild type HIV1 RT using poly(rA)/oligo(dT)16 as template after 40 mins by spectrofluorometric analysis


Eur J Med Chem 65: 134-43 (2013)


Article DOI: 10.1016/j.ejmech.2013.04.052
BindingDB Entry DOI: 10.7270/Q2736TTS
More data for this
Ligand-Target Pair