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BDBM319640 2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4- [5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]pyridine::US10174003, Example 59::US9896436, Example 59

SMILES: CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F

InChI Key: InChIKey=LAHJCVJYCGEQRW-UHFFFAOYSA-N

Data: 8 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 319640   
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
Lysine-specific demethylase 2B


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
PDB

UniProtKB/SwissProt

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PC sid
UniChem
US Patent
n/an/a 550n/an/an/an/an/an/a



Celgene Quanticel Research, Inc.

US Patent


Assay Description
The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...


US Patent US10174003 (2019)


BindingDB Entry DOI: 10.7270/Q2417053
More data for this
Ligand-Target Pair
Lysine-specific demethylase 5B


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
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n/an/a<100n/an/an/an/an/an/a



Celgene Quanticel Research, Inc.

US Patent


Assay Description
The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...


US Patent US10174003 (2019)


BindingDB Entry DOI: 10.7270/Q2417053
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
PDB

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Celgene Quanticel Research, Inc.

US Patent


Assay Description
The ability of test compounds to inhibit the activity of JMJD2C was determined in 384-well plate format under the following reaction conditions: 0.3 ...


US Patent US10174003 (2019)


BindingDB Entry DOI: 10.7270/Q2417053
More data for this
Ligand-Target Pair
Lysine-specific demethylase 6B


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
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GSK



Assay Description
The ability of test compounds to inhibit the activity of JMJD3 was determined in 384-well plate format under the following reaction conditions: 1 nM ...


Bioorg Med Chem Lett 17: 1584-9 (2007)


BindingDB Entry DOI: 10.7270/Q2FT8PBQ
More data for this
Ligand-Target Pair
Lysine-specific demethylase 2B


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
PDB

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US Patent
n/an/a 300n/an/an/an/an/an/a



GSK



Assay Description
The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...


Bioorg Med Chem Lett 17: 1584-9 (2007)


BindingDB Entry DOI: 10.7270/Q2FT8PBQ
More data for this
Ligand-Target Pair
Lysine-specific demethylase 5B


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
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n/an/a<100n/an/an/an/an/an/a



GSK



Assay Description
The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...


Bioorg Med Chem Lett 17: 1584-9 (2007)


BindingDB Entry DOI: 10.7270/Q2FT8PBQ
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
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GSK



Assay Description
The ability of test compounds to inhibit the activity of JMJD2C was determined in 384-well plate format under the following reaction conditions: 0.3 ...


Bioorg Med Chem Lett 17: 1584-9 (2007)


BindingDB Entry DOI: 10.7270/Q2FT8PBQ
More data for this
Ligand-Target Pair
Lysine-specific demethylase 6B


(Homo sapiens (Human))
BDBM319640
PNG
(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)
Show SMILES CCOc1ccccc1CCn1cnc(c1)-c1cc(ccn1)-c1nn[nH]c1C(F)(F)F
Show InChI InChI=1S/C21H19F3N6O/c1-2-31-18-6-4-3-5-14(18)8-10-30-12-17(26-13-30)16-11-15(7-9-25-16)19-20(21(22,23)24)28-29-27-19/h3-7,9,11-13H,2,8,10H2,1H3,(H,27,28,29)
PDB

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US Patent
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Celgene Quanticel Research, Inc.

US Patent


Assay Description
The ability of test compounds to inhibit the activity of JMJD3 was determined in 384-well plate format under the following reaction conditions: 1 nM ...


US Patent US10174003 (2019)


BindingDB Entry DOI: 10.7270/Q2417053
More data for this
Ligand-Target Pair