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BDBM50512014 CHEMBL4532838

SMILES: CCOc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(=O)NCCN1CCOCC1

InChI Key: InChIKey=YSHOSOFOQHTGID-UHFFFAOYSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:
   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 = 50512014   
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


(Rattus norvegicus)
BDBM50512014
PNG
(CHEMBL4532838)
Show SMILES CCOc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(=O)NCCN1CCOCC1
Show InChI InChI=1S/C24H29N5O5S/c1-2-34-20-7-3-18(4-8-20)23-17-22(24(30)26-11-12-28-13-15-33-16-14-28)27-29(23)19-5-9-21(10-6-19)35(25,31)32/h3-10,17H,2,11-16H2,1H3,(H,26,30)(H2,25,31,32)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 860n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of Sprague-Dawley rat 5-LOX assessed as calcium ionophore A23187-stimulated LTB4 production preincubated for 30 mins followed by calcium i...


Eur J Med Chem 169: 168-184 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.008
More data for this
Ligand-Target Pair
Prostaglandin E synthase/G/H synthase 2


(Homo sapiens (Human))
BDBM50512014
PNG
(CHEMBL4532838)
Show SMILES CCOc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(=O)NCCN1CCOCC1
Show InChI InChI=1S/C24H29N5O5S/c1-2-34-20-7-3-18(4-8-20)23-17-22(24(30)26-11-12-28-13-15-33-16-14-28)27-29(23)19-5-9-21(10-6-19)35(25,31)32/h3-10,17H,2,11-16H2,1H3,(H,26,30)(H2,25,31,32)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 850n/an/an/an/an/an/a



Nanjing University

Curated by ChEMBL


Assay Description
Inhibition of COX2 (unknown origin) using arachidonic acid as substrate incubated for 10 mins by Ellman's reagent based COX-1/COX-2 ELISA assay


Eur J Med Chem 169: 168-184 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.008
More data for this
Ligand-Target Pair