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BDBM50508786 CHEMBL4441079

SMILES: CCn1c2c(Oc3cc(ccn3)C#N)cccc2[nH]c1=O

InChI Key: InChIKey=UHCLQRVKFKAXKS-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50508786   
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)
BDBM50508786
PNG
(CHEMBL4441079)
Show SMILES CCn1c2c(Oc3cc(ccn3)C#N)cccc2[nH]c1=O
Show InChI InChI=1S/C15H12N4O2/c1-2-19-14-11(18-15(19)20)4-3-5-12(14)21-13-8-10(9-16)6-7-17-13/h3-8H,2H2,1H3,(H,18,20)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.36E+3n/an/an/an/an/an/a



Stellenbosch University

Curated by ChEMBL


Assay Description
Inhibition of wild-type HIV1 reverse transcriptase in HIV1 infected HEK293T cells harboring luciferase gene assessed as reduction in viral infection ...


ACS Med Chem Lett 10: 196-202 (2019)


Article DOI: 10.1021/acsmedchemlett.8b00549
More data for this
Ligand-Target Pair