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SMILES: Cc1sc2nc([nH]c(=O)c2c1C)-c1ccc(O)c(O)c1

InChI Key: InChIKey=YKOJOEIHXHEWTI-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50492114   
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)		BDBM50492114
PNG
(CHEMBL2397283)
Show SMILES Cc1sc2nc([nH]c(=O)c2c1C)-c1ccc(O)c(O)c1
Show InChI InChI=1S/C14H12N2O3S/c1-6-7(2)20-14-11(6)13(19)15-12(16-14)8-3-4-9(17)10(18)5-8/h3-5,17-18H,1-2H3,(H,15,16,19)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
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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