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BDBM50364919 CHEMBL1508899

SMILES: COc1ccc2[nH]c(C(O)=O)c(CCC(O)=O)c2c1

InChI Key: InChIKey=GOWUBWYAUQFOOY-UHFFFAOYSA-N

Data: 1 IC50  1 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50364919   
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
Uracil nucleotide/cysteinyl leukotriene receptor


(Homo sapiens (Human))
BDBM50364919
PNG
(CHEMBL1508899)
Show SMILES COc1ccc2[nH]c(C(O)=O)c(CCC(O)=O)c2c1
Show InChI InChI=1S/C13H13NO5/c1-19-7-2-4-10-9(6-7)8(3-5-11(15)16)12(14-10)13(17)18/h2,4,6,14H,3,5H2,1H3,(H,15,16)(H,17,18)
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PC cid
PC sid
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Similars

Article
PubMed
n/an/an/an/a>3.00E+4n/an/an/an/a



Sultan Qaboos University

Curated by ChEMBL


Assay Description
Agonist activity at human GPR17 expressed in human 1321N1 cells assessed as induction of calcium mobilization after 1 hr by Oregon Green BAPTA-1/AM d...


J Med Chem 61: 8136-8154 (2018)


Article DOI: 10.1021/acs.jmedchem.7b01768
BindingDB Entry DOI: 10.7270/Q28C9ZWJ
More data for this
Ligand-Target Pair
Kynurenine Aminotransferase 1/Glutamine Transaminase K


(Homo sapiens (Human))
BDBM50364919
PNG
(CHEMBL1508899)
Show SMILES COc1ccc2[nH]c(C(O)=O)c(CCC(O)=O)c2c1
Show InChI InChI=1S/C13H13NO5/c1-19-7-2-4-10-9(6-7)8(3-5-11(15)16)12(14-10)13(17)18/h2,4,6,14H,3,5H2,1H3,(H,15,16)(H,17,18)
PDB
MMDB

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antibodypedia
GoogleScholar
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>6.00E+6n/an/an/an/an/an/a



The University of Sydney

Curated by ChEMBL


Assay Description
Inhibition of human recombinant KAT1 after 20 mins by RP-HPLC analysis


Bioorg Med Chem Lett 22: 1579-81 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.138
BindingDB Entry DOI: 10.7270/Q2891693
More data for this
Ligand-Target Pair