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BDBM50260465 CHEMBL4101003

SMILES: CN1C=CC(C=C1)C1OC(=CN1c1ccc(cc1)S(N)(=O)=O)C(F)(F)F

InChI Key: InChIKey=UVTRMYKFOQILHR-UHFFFAOYSA-N

Data: 2 IC50

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   Substructure
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50260465   
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
Cyclooxygenase


(RAT)
BDBM50260465
PNG
(CHEMBL4101003)
Show SMILES CN1C=CC(C=C1)C1OC(=CN1c1ccc(cc1)S(N)(=O)=O)C(F)(F)F |c:2,5,10|
Show InChI InChI=1S/C16H16F3N3O3S/c1-21-8-6-11(7-9-21)15-22(10-14(25-15)16(17,18)19)12-2-4-13(5-3-12)26(20,23)24/h2-11,15H,1H3,(H2,20,23,24)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 0.0530n/an/an/an/an/an/a



Chongqing Normal University

Curated by ChEMBL


Assay Description
Inhibition of COX-2 in rat peritoneal macrophages assessed as reduction in PGE2 production using radiolabelled-arachidonic acid as substrate pretreat...


Bioorg Med Chem 25: 4887-4893 (2017)


Article DOI: 10.1016/j.bmc.2017.07.038
BindingDB Entry DOI: 10.7270/Q2KW5JGN
More data for this
Ligand-Target Pair
Cyclooxygenase


(RAT)
BDBM50260465
PNG
(CHEMBL4101003)
Show SMILES CN1C=CC(C=C1)C1OC(=CN1c1ccc(cc1)S(N)(=O)=O)C(F)(F)F |c:2,5,10|
Show InChI InChI=1S/C16H16F3N3O3S/c1-21-8-6-11(7-9-21)15-22(10-14(25-15)16(17,18)19)12-2-4-13(5-3-12)26(20,23)24/h2-11,15H,1H3,(H2,20,23,24)
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 50n/an/an/an/an/an/a



Chongqing Normal University

Curated by ChEMBL


Assay Description
Inhibition of COX-1 in rat peritoneal macrophages assessed as reduction in [125I]-6-Keto-PGF1alpha production using arachidonic acid as substrate pre...


Bioorg Med Chem 25: 4887-4893 (2017)


Article DOI: 10.1016/j.bmc.2017.07.038
BindingDB Entry DOI: 10.7270/Q2KW5JGN
More data for this
Ligand-Target Pair