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SMILES: [Na+].CCc1cc(C(C)=O)c(O)cc1OCCCOc1cccc(Oc2cccc(c2)C([O-])=O)c1

InChI Key: InChIKey=UXQFZHNXQGLALU-UHFFFAOYSA-M

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50212628   
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
Leukotriene B4 receptor 1/2


(Homo sapiens (Human))
BDBM50212628
PNG
(CHEMBL59656)
Show SMILES [Na+].CCc1cc(C(C)=O)c(O)cc1OCCCOc1cccc(Oc2cccc(c2)C([O-])=O)c1
Show InChI InChI=1S/C26H26O7/c1-3-18-14-23(17(2)27)24(28)16-25(18)32-12-6-11-31-20-8-5-10-22(15-20)33-21-9-4-7-19(13-21)26(29)30/h4-5,7-10,13-16,28H,3,6,11-12H2,1-2H3,(H,29,30)/p-1
PDB

UniProtKB/SwissProt

antibodypedia
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
n/an/a 460n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of specific binding of [3H]LTB4 to LTB4 receptor in human neutrophils


Citation and Details

BindingDB Entry DOI: 10.7270/Q23N25HN
More data for this
Ligand-Target Pair
Leukotriene B4 receptor 1/2


(Homo sapiens (Human))
BDBM50212628
PNG
(CHEMBL59656)
Show SMILES [Na+].CCc1cc(C(C)=O)c(O)cc1OCCCOc1cccc(Oc2cccc(c2)C([O-])=O)c1
Show InChI InChI=1S/C26H26O7/c1-3-18-14-23(17(2)27)24(28)16-25(18)32-12-6-11-31-20-8-5-10-22(15-20)33-21-9-4-7-19(13-21)26(29)30/h4-5,7-10,13-16,28H,3,6,11-12H2,1-2H3,(H,29,30)/p-1
PDB

UniProtKB/SwissProt

antibodypedia
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
140n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition of specific binding of [3H]-LTB4 to LTB4 receptor in guinea pig lung membranes


Citation and Details

BindingDB Entry DOI: 10.7270/Q23N25HN
More data for this
Ligand-Target Pair