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BDBM50519566 CHEMBL4565208

SMILES: COc1cc(cnc1C(=O)[C@H]1C[C@@H]1C(O)=O)N(Cc1ccc(F)cc1)c1cccc(c1)C(F)(F)F

InChI Key: InChIKey=MUYPZCFQVDTEIT-PMACEKPBSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50519566   
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
Leukotriene C4 synthase


(Homo sapiens (Human))
BDBM50519566
PNG
(CHEMBL4565208)
Show SMILES COc1cc(cnc1C(=O)[C@H]1C[C@@H]1C(O)=O)N(Cc1ccc(F)cc1)c1cccc(c1)C(F)(F)F |r|
Show InChI InChI=1S/C25H20F4N2O4/c1-35-21-10-18(12-30-22(21)23(32)19-11-20(19)24(33)34)31(13-14-5-7-16(26)8-6-14)17-4-2-3-15(9-17)25(27,28)29/h2-10,12,19-20H,11,13H2,1H3,(H,33,34)/t19-,20-/m0/s1
PDB
MMDB

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UniProtKB/SwissProt

B.MOAD
DrugBank
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GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 157n/an/an/an/an/an/a



Orexo AB

Curated by ChEMBL


Assay Description
Inhibition of LTC4S in zymosan-stimulated human PBMC assessed as inhibition of LTC4 production preincubated for 45 mins followed by zymosan stimulati...


J Med Chem 62: 7769-7787 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00555
More data for this
Ligand-Target Pair
Leukotriene C4 synthase


(Homo sapiens (Human))
BDBM50519566
PNG
(CHEMBL4565208)
Show SMILES COc1cc(cnc1C(=O)[C@H]1C[C@@H]1C(O)=O)N(Cc1ccc(F)cc1)c1cccc(c1)C(F)(F)F |r|
Show InChI InChI=1S/C25H20F4N2O4/c1-35-21-10-18(12-30-22(21)23(32)19-11-20(19)24(33)34)31(13-14-5-7-16(26)8-6-14)17-4-2-3-15(9-17)25(27,28)29/h2-10,12,19-20H,11,13H2,1H3,(H,33,34)/t19-,20-/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 14n/an/an/an/an/an/a



Orexo AB

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal His6-tagged LTC4S expressed in Pichia pastoris X33 using LTA4 methyl ester and glutathione as substrate preincubated f...


J Med Chem 62: 7769-7787 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00555
More data for this
Ligand-Target Pair