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SMILES: Oc1ccc(cc1O)-c1nc2sc3CCCCCCc3c2c(=O)[nH]1

InChI Key: InChIKey=NOCNQVXXENXLPI-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50492104   
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)		BDBM50492104
PNG
(CHEMBL2397405)
Show SMILES Oc1ccc(cc1O)-c1nc2sc3CCCCCCc3c2c(=O)[nH]1
Show InChI InChI=1S/C18H18N2O3S/c21-12-8-7-10(9-13(12)22)16-19-17(23)15-11-5-3-1-2-4-6-14(11)24-18(15)20-16/h7-9,21-22H,1-6H2,(H,19,20,23)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 260n/an/an/an/an/an/a



National Cancer Institute

Curated by ChEMBL


Assay Description
Inhibition of RNase H activity of wild type HIV-1 reverse transcriptase using 18 nucleotide 3'-fluorescein-labeled RNA/18 nucleotide 5'-dabsyl-labele...

J Med Chem 56: 5436-45 (2013)


Article DOI: 10.1021/jm400405z
BindingDB Entry DOI: 10.7270/Q2B27Z7S
More data for this
Ligand-Target Pair