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SMILES: CNc1nc(Nc2ccc(C)cc2)nc(Nc2ccc(C)cc2)n1

InChI Key: InChIKey=QHOKRYUWHHKKFG-UHFFFAOYSA-N

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50161822   
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)
BDBM50161822
PNG
(CHEMBL3787152)
Show SMILES CNc1nc(Nc2ccc(C)cc2)nc(Nc2ccc(C)cc2)n1
Show InChI InChI=1S/C18H20N6/c1-12-4-8-14(9-5-12)20-17-22-16(19-3)23-18(24-17)21-15-10-6-13(2)7-11-15/h4-11H,1-3H3,(H3,19,20,21,22,23,24)
PDB
MMDB

UniProtKB/TrEMBL

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CHEMBL
PC cid
PC sid
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Patents


Similars

PubMed
n/an/a>2.00E+5n/an/an/an/an/an/a



University of Tartu

Curated by ChEMBL


Assay Description
Inhibition of HIV1 reverse transcriptase using 234-nt long RNA/18-mer DNA oligonucleotide as template/primer preincubated for 15 mins followed by inc...


Bioorg Med Chem 24: 2519-29 (2016)


BindingDB Entry DOI: 10.7270/Q2NC632Q
More data for this
Ligand-Target Pair
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50161822
PNG
(CHEMBL3787152)
Show SMILES CNc1nc(Nc2ccc(C)cc2)nc(Nc2ccc(C)cc2)n1
Show InChI InChI=1S/C18H20N6/c1-12-4-8-14(9-5-12)20-17-22-16(19-3)23-18(24-17)21-15-10-6-13(2)7-11-15/h4-11H,1-3H3,(H3,19,20,21,22,23,24)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a>2.00E+5n/an/an/an/an/an/a



University of Tartu

Curated by ChEMBL


Assay Description
Inhibition of HIV1 reverse transcriptase using 234-nt long RNA/18-mer DNA oligonucleotide as template/primer preincubated for 15 mins followed by inc...


Bioorg Med Chem 24: 2519-29 (2016)


BindingDB Entry DOI: 10.7270/Q2NC632Q
More data for this
Ligand-Target Pair