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BDBM50262236 CHEMBL4081391

SMILES: CCCCCCc1c(C(=O)CC2(CC(O)=O)CC2)c2cc(Cl)ccc2n1C

InChI Key: InChIKey=MNJIVPMZNMUMAC-UHFFFAOYSA-N

Data: 1 IC50

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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 1 hit for monomerid = 50262236   
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
TG 1019


(Homo sapiens (Human))
BDBM50262236
PNG
(CHEMBL4081391)
Show SMILES CCCCCCc1c(C(=O)CC2(CC(O)=O)CC2)c2cc(Cl)ccc2n1C
Show InChI InChI=1S/C22H28ClNO3/c1-3-4-5-6-7-18-21(16-12-15(23)8-9-17(16)24(18)2)19(25)13-22(10-11-22)14-20(26)27/h8-9,12H,3-7,10-11,13-14H2,1-2H3,(H,26,27)
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 580n/an/an/an/an/an/a



Claude Pepper Institute and Department of Chemistry, Florida Institute of Technology, 150 West University Boulevard, Melbourne, FL 32901, USA.

Curated by ChEMBL


Assay Description
Antagonist activity at OXE receptor in human neutrophils assessed as inhibition of 5-oxo-ETE-induced calcium mobilization incubated for 2 mins follow...


Bioorg Med Chem Lett 27: 4770-4776 (2017)


Article DOI: 10.1016/j.bmcl.2017.08.034
BindingDB Entry DOI: 10.7270/Q2W098DS
More data for this
Ligand-Target Pair