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SMILES: CCCCCCCCCCCCc1ccccc1C(SCCC(O)=O)[S+]([O-])CCC(O)=O

InChI Key: InChIKey=FYTRQOCBJGGXJC-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50226360   
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
Cysteinyl leukotriene receptor 1/2


(Homo sapiens (Human))		BDBM50226360
PNG
(CHEMBL33764)
Show SMILES CCCCCCCCCCCCc1ccccc1C(SCCC(O)=O)[S+]([O-])CCC(O)=O
Show InChI InChI=1S/C25H40O5S2/c1-2-3-4-5-6-7-8-9-10-11-14-21-15-12-13-16-22(21)25(31-19-17-23(26)27)32(30)20-18-24(28)29/h12-13,15-16,25H,2-11,14,17-20H2,1H3,(H,26,27)(H,28,29)
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Similars
PubMed
 423n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound is evaluated for its ability to inhibit [3H]LTD4 binding to Cysteinyl leukotriene D4 receptor in guinea pig lung membranes

J Med Chem 29: 1442-52 (1986)


BindingDB Entry DOI: 10.7270/Q2S75JHD
More data for this
Ligand-Target Pair