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Compile Data Set for Download or QSAR

Found 2 hits with Last Name = 'lee' and Initial = 'rh'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50436447
PNG
(CHEMBL2397162)
Show SMILES COc1ccccc1COc1ccccc1C=CC=C1SC(S)=NC1=O |w:16.17,18.19,c:24|
Show InChI InChI=1S/C20H17NO3S2/c1-23-16-10-4-3-8-15(16)13-24-17-11-5-2-7-14(17)9-6-12-18-19(22)21-20(25)26-18/h2-12H,13H2,1H3,(H,21,22,25)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 800n/an/an/an/an/an/a



University of Science and Technology

Curated by ChEMBL


Assay Description
Inhibition of human His6-tagged full length PRL3 assessed as inhibition of DiFMUP dephosphorylation


Bioorg Med Chem Lett 23: 3769-74 (2013)


Article DOI: 10.1016/j.bmcl.2013.04.092
BindingDB Entry DOI: 10.7270/Q2QR4ZHJ
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50184288
PNG
(5-(2-(2-bromobenzyloxy)-5-bromobenzylidene)-2-thio...)
Show SMILES SC1=NC(=O)C(S1)=Cc1cc(Br)ccc1OCc1ccccc1Br |w:7.8,t:1|
Show InChI InChI=1S/C17H11Br2NO2S2/c18-12-5-6-14(22-9-10-3-1-2-4-13(10)19)11(7-12)8-15-16(21)20-17(23)24-15/h1-8H,9H2,(H,20,21,23)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.10E+3n/an/an/an/an/an/a



University of Science and Technology

Curated by ChEMBL


Assay Description
Inhibition of human His6-tagged full length PRL3 assessed as inhibition of DiFMUP dephosphorylation


Bioorg Med Chem Lett 23: 3769-74 (2013)


Article DOI: 10.1016/j.bmcl.2013.04.092
BindingDB Entry DOI: 10.7270/Q2QR4ZHJ
More data for this
Ligand-Target Pair