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28 similar compounds to monomer 50440570

Compile data set for download or QSAR
Wt: 336.4
BDBM9388
Wt: 350.4
BDBM9393
Wt: 350.4
BDBM9414
Wt: 362.5
BDBM54816
Wt: 348.4
BDBM60276
Wt: 344.4
BDBM50192179
Purchase
Wt: 358.4
BDBM50203376
Wt: 344.4
BDBM50203383
Purchase
Wt: 344.4
BDBM50203468
Wt: 322.4
BDBM50218209
Wt: 488.6
BDBM50440562
Wt: 466.6
BDBM50440571
Purchase
Wt: 410.5
BDBM50440574
Wt: 466.6
BDBM50440576
Wt: 396.5
BDBM50440578
Displayed 1 to 15 (of 28 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 84 hits for monomerid = 9388,9393,9414,54816,60276,50192179,50203376,50203383,50203468,50218209,50440562,50440571,50440574,50440576,50440578   
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
Dopamine receptors; D2 & D4


(Homo sapiens (Human))
BDBM50203383
PNG
(CHEMBL228972 | N-(1-benzylpiperidin-4-yl)-2-naphth...)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)24-22-12-14-25(15-13-22)17-18-6-2-1-3-7-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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11n/an/an/an/an/an/an/an/a



Université du Droit et de la Santé Lille II

Curated by ChEMBL


Assay Description
Displacement of [3H]nemonapride from human cloned dopamine D4.2 receptor


Bioorg Med Chem Lett 17: 1570-4 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.106
BindingDB Entry DOI: 10.7270/Q2Z037T3
More data for this
Ligand-Target Pair
Dopamine receptors; D2 & D4


(Homo sapiens (Human))
BDBM50203383
PNG
(CHEMBL228972 | N-(1-benzylpiperidin-4-yl)-2-naphth...)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)24-22-12-14-25(15-13-22)17-18-6-2-1-3-7-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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11n/an/an/an/an/an/an/an/a



Faculté des Sciences Pharmaceutiques et Biologiques de Lille

Curated by ChEMBL


Assay Description
Displacement of [3H]nemonapride from human cloned dopamine D4.2 receptor


Bioorg Med Chem Lett 17: 1565-9 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.096
BindingDB Entry DOI: 10.7270/Q2T72H3S
More data for this
Ligand-Target Pair
Dopamine receptors; D2 & D4


(Homo sapiens (Human))
BDBM50203376
PNG
(CHEMBL234826 | naphthalene-2-carboxylic acid [1-(4...)
Show SMILES Cc1ccc(CN2CCC(CC2)NC(=O)c2ccc3ccccc3c2)cc1
Show InChI InChI=1S/C24H26N2O/c1-18-6-8-19(9-7-18)17-26-14-12-23(13-15-26)25-24(27)22-11-10-20-4-2-3-5-21(20)16-22/h2-11,16,23H,12-15,17H2,1H3,(H,25,27)
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21n/an/an/an/an/an/an/an/a



Université du Droit et de la Santé Lille II

Curated by ChEMBL


Assay Description
Displacement of [3H]nemonapride from human cloned dopamine D4.2 receptor


Bioorg Med Chem Lett 17: 1570-4 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.106
BindingDB Entry DOI: 10.7270/Q2Z037T3
More data for this
Ligand-Target Pair
Serotonin (5-HT) receptor


(Rattus norvegicus (rat))
BDBM50203383
PNG
(CHEMBL228972 | N-(1-benzylpiperidin-4-yl)-2-naphth...)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)24-22-12-14-25(15-13-22)17-18-6-2-1-3-7-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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44n/an/an/an/an/an/an/an/a



Université du Droit et de la Santé Lille II

Curated by ChEMBL


Assay Description
Displacement of [3H]ketanserin from rat 5HT2A receptor


Bioorg Med Chem Lett 17: 1570-4 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.106
BindingDB Entry DOI: 10.7270/Q2Z037T3
More data for this
Ligand-Target Pair
Serotonin (5-HT) receptor


(Rattus norvegicus (rat))
BDBM50203383
PNG
(CHEMBL228972 | N-(1-benzylpiperidin-4-yl)-2-naphth...)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)24-22-12-14-25(15-13-22)17-18-6-2-1-3-7-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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44n/an/an/an/an/an/an/an/a



Faculté des Sciences Pharmaceutiques et Biologiques de Lille

Curated by ChEMBL


Assay Description
Displacement of [3H]ketanserin from rat cloned 5HT2A receptor


Bioorg Med Chem Lett 17: 1565-9 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.096
BindingDB Entry DOI: 10.7270/Q2T72H3S
More data for this
Ligand-Target Pair
Dopamine receptors; D2 & D4


(Homo sapiens (Human))
BDBM50203468
PNG
((4-(benzylamino)piperidin-1-yl)(naphthalen-2-yl)me...)
Show SMILES O=C(N1CCC(CC1)NCc1ccccc1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)25-14-12-22(13-15-25)24-17-18-6-2-1-3-7-18/h1-11,16,22,24H,12-15,17H2
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167n/an/an/an/an/an/an/an/a



Faculté des Sciences Pharmaceutiques et Biologiques de Lille

Curated by ChEMBL


Assay Description
Displacement of [3H]nemonapride from human cloned dopamine D4.2 receptor


Bioorg Med Chem Lett 17: 1565-9 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.096
BindingDB Entry DOI: 10.7270/Q2T72H3S
More data for this
Ligand-Target Pair
Serotonin (5-HT) receptor


(Rattus norvegicus (rat))
BDBM50203376
PNG
(CHEMBL234826 | naphthalene-2-carboxylic acid [1-(4...)
Show SMILES Cc1ccc(CN2CCC(CC2)NC(=O)c2ccc3ccccc3c2)cc1
Show InChI InChI=1S/C24H26N2O/c1-18-6-8-19(9-7-18)17-26-14-12-23(13-15-26)25-24(27)22-11-10-20-4-2-3-5-21(20)16-22/h2-11,16,23H,12-15,17H2,1H3,(H,25,27)
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222n/an/an/an/an/an/an/an/a



Université du Droit et de la Santé Lille II

Curated by ChEMBL


Assay Description
Displacement of [3H]ketanserin from rat 5HT2A receptor


Bioorg Med Chem Lett 17: 1570-4 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.106
BindingDB Entry DOI: 10.7270/Q2Z037T3
More data for this
Ligand-Target Pair
Melanin-concentrating hormone receptor


(Homo sapiens (Human))
BDBM50192179
PNG
(CHEMBL215388 | N-(1-(naphthalen-2-ylmethyl)piperid...)
Show SMILES O=C(NC1CCN(Cc2ccc3ccccc3c2)CC1)c1ccccc1
Show InChI InChI=1S/C23H24N2O/c26-23(20-7-2-1-3-8-20)24-22-12-14-25(15-13-22)17-18-10-11-19-6-4-5-9-21(19)16-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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347n/an/an/an/an/an/an/an/a



Procter and Gamble Pharmaceuticals

Curated by ChEMBL


Assay Description
Binding activity against human MCH-R1


Bioorg Med Chem Lett 16: 5445-50 (2006)


Article DOI: 10.1016/j.bmcl.2006.07.053
BindingDB Entry DOI: 10.7270/Q2CR5T0F
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50203383
PNG
(CHEMBL228972 | N-(1-benzylpiperidin-4-yl)-2-naphth...)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)24-22-12-14-25(15-13-22)17-18-6-2-1-3-7-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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>1.00E+3n/an/an/an/an/an/an/an/a



Université du Droit et de la Santé Lille II

Curated by ChEMBL


Assay Description
Displacement of [3H]spiperone from human cloned dopamine D2L receptor


Bioorg Med Chem Lett 17: 1570-4 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.106
BindingDB Entry DOI: 10.7270/Q2Z037T3
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50203383
PNG
(CHEMBL228972 | N-(1-benzylpiperidin-4-yl)-2-naphth...)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C23H24N2O/c26-23(21-11-10-19-8-4-5-9-20(19)16-21)24-22-12-14-25(15-13-22)17-18-6-2-1-3-7-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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>1.00E+3n/an/an/an/an/an/an/an/a



Faculté des Sciences Pharmaceutiques et Biologiques de Lille

Curated by ChEMBL


Assay Description
Displacement of [3H]spiperone from human cloned dopamine D2L receptor


Bioorg Med Chem Lett 17: 1565-9 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.096
BindingDB Entry DOI: 10.7270/Q2T72H3S
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Mus musculus (mouse))
BDBM9388
PNG
(N-[2-(1-benzylpiperidin-4-yl)ethyl]-4-methylbenzam...)
Show SMILES Cc1ccc(cc1)C(=O)NCCC1CCN(Cc2ccccc2)CC1
Show InChI InChI=1S/C22H28N2O/c1-18-7-9-21(10-8-18)22(25)23-14-11-19-12-15-24(16-13-19)17-20-5-3-2-4-6-20/h2-10,19H,11-17H2,1H3,(H,23,25)
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n/an/a 180n/an/an/an/a7.425



Tsukuba Research Laboratories



Assay Description
The cholinesterase assays were performed using colorimetric method reported by Ellman. The amount of a yellow substance formed after incubation was d...


J Med Chem 33: 1880-7 (1990)


Article DOI: 10.1021/jm00169a008
BindingDB Entry DOI: 10.7270/Q20Z71H2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Mus musculus (mouse))
BDBM9393
PNG
(CHEMBL56586 | N-[2-(1-benzylpiperidin-4-yl)ethyl]-...)
Show SMILES O=Cc1ccc(cc1)C(=O)NCCC1CCN(Cc2ccccc2)CC1
Show InChI InChI=1S/C22H26N2O2/c25-17-20-6-8-21(9-7-20)22(26)23-13-10-18-11-14-24(15-12-18)16-19-4-2-1-3-5-19/h1-9,17-18H,10-16H2,(H,23,26)
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n/an/a 120n/an/an/an/a7.425



Tsukuba Research Laboratories



Assay Description
The cholinesterase assays were performed using colorimetric method reported by Ellman. The amount of a yellow substance formed after incubation was d...


J Med Chem 33: 1880-7 (1990)


Article DOI: 10.1021/jm00169a008
BindingDB Entry DOI: 10.7270/Q20Z71H2
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Mus musculus (mouse))
BDBM9414
PNG
(CHEMBL127097 | N-methyl-N-(2-{1-[(4-methylphenyl)m...)
Show SMILES CN(CCC1CCN(Cc2ccc(C)cc2)CC1)C(=O)c1ccccc1
Show InChI InChI=1S/C23H30N2O/c1-19-8-10-21(11-9-19)18-25-16-13-20(14-17-25)12-15-24(2)23(26)22-6-4-3-5-7-22/h3-11,20H,12-18H2,1-2H3
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n/an/a 4.10E+4n/an/an/an/an/an/a



Tsukuba Research Laboratories



Assay Description
The cholinesterase assays were performed using colorimetric method reported by Ellman. The amount of a yellow substance formed after incubation was d...


J Med Chem 33: 1880-7 (1990)


Article DOI: 10.1021/jm00169a008
BindingDB Entry DOI: 10.7270/Q20Z71H2
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/a 824n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2009)


BindingDB Entry DOI: 10.7270/Q2765CR5
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/a 2.62E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2009)


BindingDB Entry DOI: 10.7270/Q20C4T6J
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM60276
PNG
(4-methyl-N-[9-(phenylmethyl)-9-azabicyclo[3.3.1]no...)
Show SMILES Cc1ccc(cc1)C(=O)NC1CC2CCCC(C1)N2Cc1ccccc1
Show InChI InChI=1S/C23H28N2O/c1-17-10-12-19(13-11-17)23(26)24-20-14-21-8-5-9-22(15-20)25(21)16-18-6-3-2-4-7-18/h2-4,6-7,10-13,20-22H,5,8-9,14-16H2,1H3,(H,24,26)
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n/an/a 8.04E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2009)


BindingDB Entry DOI: 10.7270/Q20C4T6J
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/a>3.20E+4n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2G44NRK
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/a 3.20E+4n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics Source Affiliation: Sanford-Burnham Medical Research Institute Network: NIH Molecular Lib...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q25T3HZB
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/an/an/a>3.20E+4n/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2NS0SBF
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/a 3.20E+4n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q28K77JP
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/an/an/a>3.20E+4n/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics Source Affiliation: Sanford-Burnham Medical Research Institute Network: NIH Molecular Lib...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q24T6GTZ
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/an/an/a>3.20E+4n/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2125R3Z
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM54816
PNG
(4-methyl-N-[9-(4-methylbenzyl)-9-azabicyclo[3.3.1]...)
Show SMILES Cc1ccc(CN2C3CCCC2CC(C3)NC(=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C24H30N2O/c1-17-6-10-19(11-7-17)16-26-22-4-3-5-23(26)15-21(14-22)25-24(27)20-12-8-18(2)9-13-20/h6-13,21-23H,3-5,14-16H2,1-2H3,(H,25,27)
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n/an/a 3.28E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2H70D7S
More data for this
Ligand-Target Pair
Tyrosinase


(Homo sapiens (Human))
BDBM50218209
PNG
(CHEMBL250773 | Tyrosinase Inhibitor, 3 | naphthale...)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C21H26N2O/c24-21(19-9-8-17-6-2-3-7-18(17)16-19)23-14-10-20(11-15-23)22-12-4-1-5-13-22/h2-3,6-9,16,20H,1,4-5,10-15H2
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n/an/a 6.64E+3n/an/an/an/a6.837



University of Karachi



Assay Description
Tyrosinase inhibition assays were performed in a 96-well microplate format using SpectraMax 340 (Molecular Devices, CA, USA) microplate reader accord...


J Enzyme Inhib Med Chem 20: 401-7 (2005)


Article DOI: 10.1080/14756360500179333
BindingDB Entry DOI: 10.7270/Q29G5KBN
More data for this
Ligand-Target Pair
Melanin-concentrating hormone receptor


(Homo sapiens (Human))
BDBM50192179
PNG
(CHEMBL215388 | N-(1-(naphthalen-2-ylmethyl)piperid...)
Show SMILES O=C(NC1CCN(Cc2ccc3ccccc3c2)CC1)c1ccccc1
Show InChI InChI=1S/C23H24N2O/c26-23(20-7-2-1-3-8-20)24-22-12-14-25(15-13-22)17-18-10-11-19-6-4-5-9-21(19)16-18/h1-11,16,22H,12-15,17H2,(H,24,26)
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n/an/a 948n/an/an/an/an/an/a



Procter and Gamble Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of MCH-mediated calcium release by CHO cells expressing human MCH-R1


Bioorg Med Chem Lett 16: 5445-50 (2006)


Article DOI: 10.1016/j.bmcl.2006.07.053
BindingDB Entry DOI: 10.7270/Q2CR5T0F
More data for this
Ligand-Target Pair
Tyrosinase


(Agaricus bisporus (Common mushroom))
BDBM50218209
PNG
(CHEMBL250773 | Tyrosinase Inhibitor, 3 | naphthale...)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc2ccccc2c1
Show InChI InChI=1S/C21H26N2O/c24-21(19-9-8-17-6-2-3-7-18(17)16-19)23-14-10-20(11-15-23)22-12-4-1-5-13-22/h2-3,6-9,16,20H,1,4-5,10-15H2
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n/an/a 6.64E+3n/an/an/an/an/an/a



Central University of Las Villas

Curated by ChEMBL


Assay Description
Inhibition of mashroom tyrosinase


Eur J Med Chem 42: 1370-81 (2007)


Article DOI: 10.1016/j.ejmech.2007.01.026
BindingDB Entry DOI: 10.7270/Q23R0TP1
More data for this
Ligand-Target Pair
MBT domain-containing protein 1 (MBTD1)


(Homo sapiens (Human))
BDBM50440562
PNG
(CHEMBL2426361)
Show SMILES O=C(N1CCC(CC1)N1CCCC1)c1ccc2cc(ccc2c1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C30H40N4O2/c35-29(33-17-9-27(10-18-33)31-13-1-2-14-31)25-7-5-24-22-26(8-6-23(24)21-25)30(36)34-19-11-28(12-20-34)32-15-3-4-16-32/h5-8,21-22,27-28H,1-4,9-20H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of MBTD1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
MBT domain-containing protein 1 (MBTD1)


(Homo sapiens (Human))
BDBM50440571
PNG
(CHEMBL2426474)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-11-25(12-20-31)29-15-3-1-4-16-29)23-7-9-24(10-8-23)28(34)32-21-13-26(14-22-32)30-17-5-2-6-18-30/h7-10,25-26H,1-6,11-22H2
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n/an/a 4.90E+3n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of MBTD1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
MBT domain-containing protein 1 (MBTD1)


(Homo sapiens (Human))
BDBM50440574
PNG
(CHEMBL2426471)
Show SMILES O=C(N1CCC(CC1)N1CCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCC1
Show InChI InChI=1S/C24H34N4O2/c29-23(27-15-7-21(8-16-27)25-11-1-12-25)19-3-5-20(6-4-19)24(30)28-17-9-22(10-18-28)26-13-2-14-26/h3-6,21-22H,1-2,7-18H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of MBTD1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
MBT domain-containing protein 1 (MBTD1)


(Homo sapiens (Human))
BDBM50440576
PNG
(CHEMBL2426469)
Show SMILES O=C(N1CCCC(CC1)N1CCCC1)c1ccc(cc1)C(=O)N1CCCC(CC1)N1CCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-5-7-25(13-21-31)29-15-1-2-16-29)23-9-11-24(12-10-23)28(34)32-20-6-8-26(14-22-32)30-17-3-4-18-30/h9-12,25-26H,1-8,13-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of MBTD1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
MBT domain-containing protein 1 (MBTD1)


(Homo sapiens (Human))
BDBM50440578
PNG
(CHEMBL2426467)
Show SMILES O=C(N1CC2CNCC2C1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C23H32N4O2/c28-22(26-11-7-21(8-12-26)25-9-1-2-10-25)17-3-5-18(6-4-17)23(29)27-15-19-13-24-14-20(19)16-27/h3-6,19-21,24H,1-2,7-16H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of MBTD1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Scm-like with four MBT domains protein 1


(Homo sapiens (Human))
BDBM50440562
PNG
(CHEMBL2426361)
Show SMILES O=C(N1CCC(CC1)N1CCCC1)c1ccc2cc(ccc2c1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C30H40N4O2/c35-29(33-17-9-27(10-18-33)31-13-1-2-14-31)25-7-5-24-22-26(8-6-23(24)21-25)30(36)34-19-11-28(12-20-34)32-15-3-4-16-32/h5-8,21-22,27-28H,1-4,9-20H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of SFMBT1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Scm-like with four MBT domains protein 1


(Homo sapiens (Human))
BDBM50440571
PNG
(CHEMBL2426474)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-11-25(12-20-31)29-15-3-1-4-16-29)23-7-9-24(10-8-23)28(34)32-21-13-26(14-22-32)30-17-5-2-6-18-30/h7-10,25-26H,1-6,11-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of SFMBT1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Scm-like with four MBT domains protein 1


(Homo sapiens (Human))
BDBM50440574
PNG
(CHEMBL2426471)
Show SMILES O=C(N1CCC(CC1)N1CCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCC1
Show InChI InChI=1S/C24H34N4O2/c29-23(27-15-7-21(8-16-27)25-11-1-12-25)19-3-5-20(6-4-19)24(30)28-17-9-22(10-18-28)26-13-2-14-26/h3-6,21-22H,1-2,7-18H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of SFMBT1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Scm-like with four MBT domains protein 1


(Homo sapiens (Human))
BDBM50440576
PNG
(CHEMBL2426469)
Show SMILES O=C(N1CCCC(CC1)N1CCCC1)c1ccc(cc1)C(=O)N1CCCC(CC1)N1CCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-5-7-25(13-21-31)29-15-1-2-16-29)23-9-11-24(12-10-23)28(34)32-20-6-8-26(14-22-32)30-17-3-4-18-30/h9-12,25-26H,1-8,13-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of SFMBT1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Scm-like with four MBT domains protein 1


(Homo sapiens (Human))
BDBM50440578
PNG
(CHEMBL2426467)
Show SMILES O=C(N1CC2CNCC2C1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C23H32N4O2/c28-22(26-11-7-21(8-12-26)25-9-1-2-10-25)17-3-5-18(6-4-17)23(29)27-15-19-13-24-14-20(19)16-27/h3-6,19-21,24H,1-2,7-16H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of SFMBT1 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440574
PNG
(CHEMBL2426471)
Show SMILES O=C(N1CCC(CC1)N1CCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCC1
Show InChI InChI=1S/C24H34N4O2/c29-23(27-15-7-21(8-16-27)25-11-1-12-25)19-3-5-20(6-4-19)24(30)28-17-9-22(10-18-28)26-13-2-14-26/h3-6,21-22H,1-2,7-18H2
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n/an/a 400n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440576
PNG
(CHEMBL2426469)
Show SMILES O=C(N1CCCC(CC1)N1CCCC1)c1ccc(cc1)C(=O)N1CCCC(CC1)N1CCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-5-7-25(13-21-31)29-15-1-2-16-29)23-9-11-24(12-10-23)28(34)32-20-6-8-26(14-22-32)30-17-3-4-18-30/h9-12,25-26H,1-8,13-22H2
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n/an/a 110n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440578
PNG
(CHEMBL2426467)
Show SMILES O=C(N1CC2CNCC2C1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C23H32N4O2/c28-22(26-11-7-21(8-12-26)25-9-1-2-10-25)17-3-5-18(6-4-17)23(29)27-15-19-13-24-14-20(19)16-27/h3-6,19-21,24H,1-2,7-16H2
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n/an/a 3.10E+3n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440562
PNG
(CHEMBL2426361)
Show SMILES O=C(N1CCC(CC1)N1CCCC1)c1ccc2cc(ccc2c1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C30H40N4O2/c35-29(33-17-9-27(10-18-33)31-13-1-2-14-31)25-7-5-24-22-26(8-6-23(24)21-25)30(36)34-19-11-28(12-20-34)32-15-3-4-16-32/h5-8,21-22,27-28H,1-4,9-20H2
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n/an/a 450n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) using H4K20me2 as substrate after 30 mins by LNCE-TR-FRET assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440571
PNG
(CHEMBL2426474)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-11-25(12-20-31)29-15-3-1-4-16-29)23-7-9-24(10-8-23)28(34)32-21-13-26(14-22-32)30-17-5-2-6-18-30/h7-10,25-26H,1-6,11-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) using H4K20me2 as substrate after 30 mins by LNCE-TR-FRET assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440574
PNG
(CHEMBL2426471)
Show SMILES O=C(N1CCC(CC1)N1CCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCC1
Show InChI InChI=1S/C24H34N4O2/c29-23(27-15-7-21(8-16-27)25-11-1-12-25)19-3-5-20(6-4-19)24(30)28-17-9-22(10-18-28)26-13-2-14-26/h3-6,21-22H,1-2,7-18H2
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n/an/a 350n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) using H4K20me2 as substrate after 30 mins by LNCE-TR-FRET assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440576
PNG
(CHEMBL2426469)
Show SMILES O=C(N1CCCC(CC1)N1CCCC1)c1ccc(cc1)C(=O)N1CCCC(CC1)N1CCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-5-7-25(13-21-31)29-15-1-2-16-29)23-9-11-24(12-10-23)28(34)32-20-6-8-26(14-22-32)30-17-3-4-18-30/h9-12,25-26H,1-8,13-22H2
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n/an/a 110n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) using H4K20me2 as substrate after 30 mins by LNCE-TR-FRET assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440578
PNG
(CHEMBL2426467)
Show SMILES O=C(N1CC2CNCC2C1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C23H32N4O2/c28-22(26-11-7-21(8-12-26)25-9-1-2-10-25)17-3-5-18(6-4-17)23(29)27-15-19-13-24-14-20(19)16-27/h3-6,19-21,24H,1-2,7-16H2
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n/an/a 3.50E+3n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) using H4K20me2 as substrate after 30 mins by LNCE-TR-FRET assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
Lethal(3)malignant brain tumor-like protein 3 (L3MBTL3)


(Homo sapiens (Human))
BDBM50440571
PNG
(CHEMBL2426474)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-11-25(12-20-31)29-15-3-1-4-16-29)23-7-9-24(10-8-23)28(34)32-21-13-26(14-22-32)30-17-5-2-6-18-30/h7-10,25-26H,1-6,11-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of L3MBTL3 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
PHD finger protein 23 (PHF23)


(Homo sapiens (Human))
BDBM50440562
PNG
(CHEMBL2426361)
Show SMILES O=C(N1CCC(CC1)N1CCCC1)c1ccc2cc(ccc2c1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C30H40N4O2/c35-29(33-17-9-27(10-18-33)31-13-1-2-14-31)25-7-5-24-22-26(8-6-23(24)21-25)30(36)34-19-11-28(12-20-34)32-15-3-4-16-32/h5-8,21-22,27-28H,1-4,9-20H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of PHF23 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
PHD finger protein 23 (PHF23)


(Homo sapiens (Human))
BDBM50440571
PNG
(CHEMBL2426474)
Show SMILES O=C(N1CCC(CC1)N1CCCCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-11-25(12-20-31)29-15-3-1-4-16-29)23-7-9-24(10-8-23)28(34)32-21-13-26(14-22-32)30-17-5-2-6-18-30/h7-10,25-26H,1-6,11-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of PHF23 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
PHD finger protein 23 (PHF23)


(Homo sapiens (Human))
BDBM50440574
PNG
(CHEMBL2426471)
Show SMILES O=C(N1CCC(CC1)N1CCC1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCC1
Show InChI InChI=1S/C24H34N4O2/c29-23(27-15-7-21(8-16-27)25-11-1-12-25)19-3-5-20(6-4-19)24(30)28-17-9-22(10-18-28)26-13-2-14-26/h3-6,21-22H,1-2,7-18H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of PHF23 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
PHD finger protein 23 (PHF23)


(Homo sapiens (Human))
BDBM50440576
PNG
(CHEMBL2426469)
Show SMILES O=C(N1CCCC(CC1)N1CCCC1)c1ccc(cc1)C(=O)N1CCCC(CC1)N1CCCC1
Show InChI InChI=1S/C28H42N4O2/c33-27(31-19-5-7-25(13-21-31)29-15-1-2-16-29)23-9-11-24(12-10-23)28(34)32-20-6-8-26(14-22-32)30-17-3-4-18-30/h9-12,25-26H,1-8,13-22H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of PHF23 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
PHD finger protein 23 (PHF23)


(Homo sapiens (Human))
BDBM50440578
PNG
(CHEMBL2426467)
Show SMILES O=C(N1CC2CNCC2C1)c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCC1
Show InChI InChI=1S/C23H32N4O2/c28-22(26-11-7-21(8-12-26)25-9-1-2-10-25)17-3-5-18(6-4-17)23(29)27-15-19-13-24-14-20(19)16-27/h3-6,19-21,24H,1-2,7-16H2
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of North Carolina at Chapel Hill

Curated by ChEMBL


Assay Description
Inhibition of PHF23 (unknown origin) after 30 mins by AlphaScreen assay


J Med Chem 56: 7358-71 (2013)


Article DOI: 10.1021/jm400919p
BindingDB Entry DOI: 10.7270/Q2B27WRP
More data for this
Ligand-Target Pair
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