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2 similar compounds to monomer 50112455

Compile data set for download or QSAR
Wt: 264.2
BDBM50112463
Wt: 187.1
BDBM50129061

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50112463,50129061   
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
Mandelate racemase


(Pseudomonas putida (g-Proteobacteria))
BDBM50129061
PNG
((R)-Hydroxy-phenyl-methanephosphonic acid anion | ...)
Show SMILES OP(O)([O-])C(=O)c1ccccc1
Show InChI InChI=1S/C7H8O4P/c8-7(12(9,10)11)6-4-2-1-3-5-6/h1-5,9-10,12H/q-1
PDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
1.10E+3n/an/an/an/an/an/a7.5n/a



Dalhousie University

Curated by ChEMBL


Assay Description
Inhibition constant against Mandelate racemase from Pseudomonas putida at pH 7.5


Bioorg Med Chem Lett 13: 2041-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00311-1
BindingDB Entry DOI: 10.7270/Q2XP75HB
More data for this
Ligand-Target Pair
Mandelate racemase (MR)


(Pseudomonas putida (g-Proteobacteria))
BDBM50129061
PNG
((R)-Hydroxy-phenyl-methanephosphonic acid anion | ...)
Show SMILES OP(O)([O-])C(=O)c1ccccc1
Show InChI InChI=1S/C7H8O4P/c8-7(12(9,10)11)6-4-2-1-3-5-6/h1-5,9-10,12H/q-1
PDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
3.40E+4n/an/an/an/an/an/a7.5n/a



Dalhousie University

Curated by ChEMBL


Assay Description
Inhibition constant against Mandelate racemase from Pseudomonas putida at pH 7.5


Bioorg Med Chem Lett 13: 2041-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00311-1
BindingDB Entry DOI: 10.7270/Q2XP75HB
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50112463
PNG
((Biphenyl-4-yl-hydroxy-methyl)-phosphonic acid | C...)
Show SMILES OP(O)(O)C(=O)c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C13H13O4P/c14-13(18(15,16)17)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,15-18H
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a>1.00E+7n/an/an/an/an/an/a



Aventis Pharma

Curated by ChEMBL


Assay Description
The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domain


Bioorg Med Chem Lett 12: 1295-8 (2002)


Article DOI: 10.1016/s0960-894x(02)00140-3
BindingDB Entry DOI: 10.7270/Q2959GW0
More data for this
Ligand-Target Pair