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BDBM50085254 1-[2-(4-Benzyl-2-chloro-phenoxy)-ethyl]-pyrrolidine::CHEMBL423811

SMILES: Clc1cc(Cc2ccccc2)ccc1OCCN1CCCC1

InChI Key: InChIKey=VARRYIIVLBTVMO-UHFFFAOYSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:
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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50085254   
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 A4 hydrolase


(Homo sapiens (Human))
BDBM50085254
PNG
(1-[2-(4-Benzyl-2-chloro-phenoxy)-ethyl]-pyrrolidin...)
Show SMILES Clc1cc(Cc2ccccc2)ccc1OCCN1CCCC1
Show InChI InChI=1S/C19H22ClNO/c20-18-15-17(14-16-6-2-1-3-7-16)8-9-19(18)22-13-12-21-10-4-5-11-21/h1-3,6-9,15H,4-5,10-14H2
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Article
PubMed
n/an/a 1.20E+3n/an/an/an/an/an/a



Gyeongsang National University (GNU)

Curated by ChEMBL


Assay Description
Inhibition of human leukotriene A4 hydrolase


Eur J Med Chem 46: 1593-603 (2011)


Article DOI: 10.1016/j.ejmech.2011.02.007
BindingDB Entry DOI: 10.7270/Q2K64JDG
More data for this
Ligand-Target Pair
Leukotriene A4 hydrolase


(Homo sapiens (Human))
BDBM50085254
PNG
(1-[2-(4-Benzyl-2-chloro-phenoxy)-ethyl]-pyrrolidin...)
Show SMILES Clc1cc(Cc2ccccc2)ccc1OCCN1CCCC1
Show InChI InChI=1S/C19H22ClNO/c20-18-15-17(14-16-6-2-1-3-7-16)8-9-19(18)22-13-12-21-10-4-5-11-21/h1-3,6-9,15H,4-5,10-14H2
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PubMed
n/an/a 1.23E+3n/an/an/an/an/an/a



Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibitory activity was determined against Leukotriene A4 hydrolase


J Med Chem 43: 721-35 (2000)


BindingDB Entry DOI: 10.7270/Q2CN74MZ
More data for this
Ligand-Target Pair
Leukotriene A4 hydrolase


(Homo sapiens (Human))
BDBM50085254
PNG
(1-[2-(4-Benzyl-2-chloro-phenoxy)-ethyl]-pyrrolidin...)
Show SMILES Clc1cc(Cc2ccccc2)ccc1OCCN1CCCC1
Show InChI InChI=1S/C19H22ClNO/c20-18-15-17(14-16-6-2-1-3-7-16)8-9-19(18)22-13-12-21-10-4-5-11-21/h1-3,6-9,15H,4-5,10-14H2
PDB
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PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibitory activity was determined for LTB4 production in human whole blood.


J Med Chem 43: 721-35 (2000)


BindingDB Entry DOI: 10.7270/Q2CN74MZ
More data for this
Ligand-Target Pair