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2 similar compounds to monomer 50275894

Compile data set for download or QSAR
Wt: 233.1
BDBM50275944
Wt: 233.1
BDBM50275890

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50275944,50275890   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Lactoperoxidase


(Homo sapiens (Human))
BDBM50275944
PNG
(CHEMBL459114 | methyl 3-ethyl-2-selenoxo-2,3-dihyd...)
Show SMILES CCn1ccn(C(=O)OC)[c]1=[Se]
Show InChI InChI=1S/C7H10N2O2Se/c1-3-8-4-5-9(6(8)12)7(10)11-2/h4-5H,3H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.53E+4n/an/an/an/an/an/a



Institute of Science

Curated by ChEMBL


Assay Description
Inhibition of lactoperoxidase (unknown origin)-catalyzed iodination of L-tyrosine assessed as 3,5-diiodo-L-tyrosine formation by HPLC


J Med Chem 51: 7313-7 (2009)


Article DOI: 10.1021/jm800894m
BindingDB Entry DOI: 10.7270/Q2Z31ZGK
More data for this
Ligand-Target Pair
Lactoperoxidase


(Homo sapiens (Human))
BDBM50275890
PNG
(CHEMBL457523 | ethyl 2,3-dihydro-3-methyl-2-seleno...)
Show SMILES CCOC(=O)n1ccn(C)[c]1=[Se]
Show InChI InChI=1S/C7H10N2O2Se/c1-3-11-7(10)9-5-4-8(2)6(9)12/h4-5H,3H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.01E+4n/an/an/an/an/an/a



Institute of Science

Curated by ChEMBL


Assay Description
Inhibition of lactoperoxidase (unknown origin)-catalyzed iodination of L-tyrosine assessed as 3,5-diiodo-L-tyrosine formation by HPLC


J Med Chem 51: 7313-7 (2009)


Article DOI: 10.1021/jm800894m
BindingDB Entry DOI: 10.7270/Q2Z31ZGK
More data for this
Ligand-Target Pair