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BDBM2259 2-Pyridinone derivative 39::3-{[(4,7-Dichlorobenzoxazol-2-yl)methyl]sulfonyl}-5-ethyl-6-methylpyridin-2(1H)-one::3-{[(4,7-dichloro-1,3-benzoxazol-2-yl)methane]sulfonyl}-5-ethyl-6-methyl-1,2-dihydropyridin-2-one::CHEMBL176637

SMILES: CCc1cc(c(=O)[nH]c1C)S(=O)(=O)Cc1nc2c(Cl)ccc(Cl)c2o1

InChI Key: InChIKey=PUZKWXILSRLVLO-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 2259   
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
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM2259
PNG
(2-Pyridinone derivative 39 | 3-{[(4,7-Dichlorobenz...)
Show SMILES CCc1cc(c(=O)[nH]c1C)S(=O)(=O)Cc1nc2c(Cl)ccc(Cl)c2o1
Show InChI InChI=1S/C16H14Cl2N2O4S/c1-3-9-6-12(16(21)19-8(9)2)25(22,23)7-13-20-14-10(17)4-5-11(18)15(14)24-13/h4-6H,3,7H2,1-2H3,(H,19,21)
PDB
MMDB

UniProtKB/TrEMBL

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

Similars

PubMed
n/an/a 205n/an/an/an/an/an/a



Merck Reserch Laboratories

Curated by ChEMBL


Assay Description
Tested for inhibition against HIV-1 RT (used (poly)rC-(oligo)dG as the template)


J Med Chem 36: 953-66 (1993)


BindingDB Entry DOI: 10.7270/Q2JW8G28
More data for this
Ligand-Target Pair
HIV-1 Reverse Transcriptase


(Human immunodeficiency virus type 1)
BDBM2259
PNG
(2-Pyridinone derivative 39 | 3-{[(4,7-Dichlorobenz...)
Show SMILES CCc1cc(c(=O)[nH]c1C)S(=O)(=O)Cc1nc2c(Cl)ccc(Cl)c2o1
Show InChI InChI=1S/C16H14Cl2N2O4S/c1-3-9-6-12(16(21)19-8(9)2)25(22,23)7-13-20-14-10(17)4-5-11(18)15(14)24-13/h4-6H,3,7H2,1-2H3,(H,19,21)
PDB
MMDB

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 205n/an/an/an/an/an/a



Merck Reserch Laboratories

Curated by ChEMBL


Assay Description
The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.


J Med Chem 36: 953-66 (1993)


BindingDB Entry DOI: 10.7270/Q2JW8G28
More data for this
Ligand-Target Pair