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BDBM50368493 CHEMBL1744158

SMILES: CC(=O)Oc1cc(cc2cc(cc(OC(C)=O)c12)S([O-])(=O)=O)S([O-])(=O)=O

InChI Key: InChIKey=GFDULYUMFINPJB-UHFFFAOYSA-L

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50368493   
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/RNaseH


(Human immunodeficiency virus 1)
BDBM50368493
PNG
(CHEMBL1744158)
Show SMILES CC(=O)Oc1cc(cc2cc(cc(OC(C)=O)c12)S([O-])(=O)=O)S([O-])(=O)=O
Show InChI InChI=1S/C14H12O10S2/c1-7(15)23-12-5-10(25(17,18)19)3-9-4-11(26(20,21)22)6-13(14(9)12)24-8(2)16/h3-6H,1-2H3,(H,17,18,19)(H,20,21,22)/p-2
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a>1.00E+6n/an/an/an/an/an/a



Universityof Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of purified HIV-2 reverse transcriptase


J Med Chem 35: 4846-53 (1992)


BindingDB Entry DOI: 10.7270/Q2M0461N
More data for this
Ligand-Target Pair
Reverse transcriptase/RNaseH


(Human immunodeficiency virus 1)
BDBM50368493
PNG
(CHEMBL1744158)
Show SMILES CC(=O)Oc1cc(cc2cc(cc(OC(C)=O)c12)S([O-])(=O)=O)S([O-])(=O)=O
Show InChI InChI=1S/C14H12O10S2/c1-7(15)23-12-5-10(25(17,18)19)3-9-4-11(26(20,21)22)6-13(14(9)12)24-8(2)16/h3-6H,1-2H3,(H,17,18,19)(H,20,21,22)/p-2
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a>1.00E+6n/an/an/an/an/an/a



Universityof Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of purified HIV-2 reverse transcriptase


J Med Chem 35: 4846-53 (1992)


BindingDB Entry DOI: 10.7270/Q2M0461N
More data for this
Ligand-Target Pair