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BDBM50161820 CHEMBL3785590

SMILES: CCOC(=O)c1[nH]c2ccc(F)cc2c1NC(=O)NC1CCCCC1

InChI Key: InChIKey=VDPXPRICBMIFGC-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50161820   
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)
BDBM50161820
PNG
(CHEMBL3785590)
Show SMILES CCOC(=O)c1[nH]c2ccc(F)cc2c1NC(=O)NC1CCCCC1
Show InChI InChI=1S/C18H22FN3O3/c1-2-25-17(23)16-15(13-10-11(19)8-9-14(13)21-16)22-18(24)20-12-6-4-3-5-7-12/h8-10,12,21H,2-7H2,1H3,(H2,20,22,24)
PDB
MMDB

UniProtKB/TrEMBL

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CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a>5.00E+4n/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