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BDBM50142747 CHEMBL3758589

SMILES: CCOC(=O)c1c(CSc2c(C)cccc2C)[nH]c2c1cc(O)c1ccccc21

InChI Key: InChIKey=UAFMBEQXTZLIGG-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50142747   
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
Arachidonate 5-lipoxygenase


(Homo sapiens (Human))
BDBM50142747
PNG
(CHEMBL3758589)
Show SMILES CCOC(=O)c1c(CSc2c(C)cccc2C)[nH]c2c1cc(O)c1ccccc21
Show InChI InChI=1S/C24H23NO3S/c1-4-28-24(27)21-18-12-20(26)16-10-5-6-11-17(16)22(18)25-19(21)13-29-23-14(2)8-7-9-15(23)3/h5-12,25-26H,4,13H2,1-3H3
PDB
MMDB

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CHEMBL
PC cid
PC sid
UniChem

Similars

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



Second University of Naples

Curated by ChEMBL


Assay Description
Inhibition of human recombinant 5-LOX expressed in Escherichia coli BL21 using arachidonic acid as substrate assessed as LTB4 formation preincubated ...


Eur J Med Chem 108: 466-75 (2016)


BindingDB Entry DOI: 10.7270/Q2BR8V14
More data for this
Ligand-Target Pair
Arachidonate 5-lipoxygenase


(Homo sapiens (Human))
BDBM50142747
PNG
(CHEMBL3758589)
Show SMILES CCOC(=O)c1c(CSc2c(C)cccc2C)[nH]c2c1cc(O)c1ccccc21
Show InChI InChI=1S/C24H23NO3S/c1-4-28-24(27)21-18-12-20(26)16-10-5-6-11-17(16)22(18)25-19(21)13-29-23-14(2)8-7-9-15(23)3/h5-12,25-26H,4,13H2,1-3H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 170n/an/an/an/an/an/a



Second University of Naples

Curated by ChEMBL


Assay Description
Inhibition of 5-LOX in human intact polymorphonuclear leukocytes preincubated for 15 mins with CaCl2, A23187 measured after 10 mins by HPLC analysis


Eur J Med Chem 108: 466-75 (2016)


BindingDB Entry DOI: 10.7270/Q2BR8V14
More data for this
Ligand-Target Pair