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BDBM50215864 CHEMBL53636

SMILES: O[C@@H]1[C@@H](Cc2ccccc2)COc2cc(ccc12)-c1cc(ccc1C(O)=O)C(O)=O

InChI Key: InChIKey=IUZVDUBXCSPZHN-HTAPYJJXSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50215864   
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


(Homo sapiens (Human))
BDBM50215864
PNG
(CHEMBL53636)
Show SMILES O[C@@H]1[C@@H](Cc2ccccc2)COc2cc(ccc12)-c1cc(ccc1C(O)=O)C(O)=O
Show InChI InChI=1S/C24H20O6/c25-22-17(10-14-4-2-1-3-5-14)13-30-21-12-15(6-9-19(21)22)20-11-16(23(26)27)7-8-18(20)24(28)29/h1-9,11-12,17,22,25H,10,13H2,(H,26,27)(H,28,29)/t17-,22+/m0/s1
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Pfizer Inc

Curated by ChEMBL


Assay Description
Compound was evaluated for its ability to inhibit [3H]LTB4 binding to LTB4 receptors on guinea pig spleen membranes


Bioorg Med Chem Lett 8: 1781-6 (1998)


Article DOI: 10.1016/s0960-894x(98)00275-3
BindingDB Entry DOI: 10.7270/Q2RR21F1
More data for this
Ligand-Target Pair