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BDBM50328021 (2-Hydroxy-benzoylamino)-acetic acid::2-(2-hydroxybenzamido)acetic acid::2-Hydroxyhippuric acid::CHEMBL586::NSC-87566::Salicyluric Acid (50-80-%)

SMILES: OC(=O)CNC(=O)c1ccccc1O

InChI Key: InChIKey=ONJSZLXSECQROL-UHFFFAOYSA-N

Data: 2 KI  2 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50328021   
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
Solute carrier family 22 member 6


(Rattus norvegicus)
BDBM50328021
PNG
((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...)
Show SMILES OC(=O)CNC(=O)c1ccccc1O
Show InChI InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
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PubMed
1.10E+4n/an/an/an/an/an/an/an/a



Kyorin University School of Medicine

Curated by ChEMBL


Assay Description
TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytes


Mol Pharmacol 55: 847-54 (1999)


BindingDB Entry DOI: 10.7270/Q28053WW
More data for this
Ligand-Target Pair
Solute carrier family 22 member 6


(Rattus norvegicus)
BDBM50328021
PNG
((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...)
Show SMILES OC(=O)CNC(=O)c1ccccc1O
Show InChI InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
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Article
PubMed
1.10E+4n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibition of rat Oat1 expressed in Xenopus oocytes


Bioorg Med Chem 19: 3320-40 (2011)


Article DOI: 10.1016/j.bmc.2011.04.045
BindingDB Entry DOI: 10.7270/Q2TB17WF
More data for this
Ligand-Target Pair
Egl nine homolog 2


(Homo sapiens (Human))
BDBM50328021
PNG
((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...)
Show SMILES OC(=O)CNC(=O)c1ccccc1O
Show InChI InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
PDB

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



University of Oxford

Curated by ChEMBL


Assay Description
Inhibition of PHD1 by HTRF assay


Bioorg Med Chem Lett 20: 6125-8 (2010)


Article DOI: 10.1016/j.bmcl.2010.08.032
BindingDB Entry DOI: 10.7270/Q22B8Z7F
More data for this
Ligand-Target Pair
Solute carrier family 22 member 6


(Homo sapiens (Human))
BDBM50328021
PNG
((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...)
Show SMILES OC(=O)CNC(=O)c1ccccc1O
Show InChI InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
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CHEMBL
KEGG
PC cid
PC sid
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Article
PubMed
n/an/a 2.70E+4n/an/an/an/an/an/a



Tokyo Women's Medical University

Curated by ChEMBL


Assay Description
TP_TRANSPORTER: inhibition of PAH uptake in OAT-expressing OK cells


Br J Pharmacol 135: 555-63 (2002)


Article DOI: 10.1038/sj.bjp.0704482
BindingDB Entry DOI: 10.7270/Q21J9C29
More data for this
Ligand-Target Pair