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BDBM15608 CHEMBL353159::N-Methyl,N-propargyl-1H-pyrrole-2-carboxamide::N-methyl-N-(prop-2-yn-1-yl)-1H-pyrrole-2-carboxamide::pyrrole inhibitor 33

SMILES: CN(CC#C)C(=O)c1ccc[nH]1

InChI Key: InChIKey=IKQLCRCMGYGVMD-UHFFFAOYSA-N

Data: 6 KI

Find this compound or compounds like it in BindingDB or PDB:
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 15608   
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
Monoamine oxidase


(Bos taurus)
BDBM15608
PNG
(CHEMBL353159 | N-Methyl,N-propargyl-1H-pyrrole-2-c...)
Show SMILES CN(CC#C)C(=O)c1ccc[nH]1
Show InChI InChI=1S/C9H10N2O/c1-3-7-11(2)9(12)8-5-4-6-10-8/h1,4-6,10H,7H2,2H3
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5.40n/an/an/an/an/an/an/an/a



Padmashri Vikhe Patil College

Curated by ChEMBL


Assay Description
Inhibition of bovine MAO-A using kinuramine as substrate by fluorometric method


Eur J Med Chem 110: 13-31 (2016)


BindingDB Entry DOI: 10.7270/Q2S75J6C
More data for this
Ligand-Target Pair
Monoamine oxidase


(Bos taurus)
BDBM15608
PNG
(CHEMBL353159 | N-Methyl,N-propargyl-1H-pyrrole-2-c...)
Show SMILES CN(CC#C)C(=O)c1ccc[nH]1
Show InChI InChI=1S/C9H10N2O/c1-3-7-11(2)9(12)8-5-4-6-10-8/h1,4-6,10H,7H2,2H3
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75n/an/an/an/an/an/an/an/a



Università degli Studi di Roma La Sapienza

Curated by ChEMBL


Assay Description
Inhibitory activity against monoamine oxidase A in isolated bovine brain mitochondria


J Med Chem 46: 917-20 (2003)


Article DOI: 10.1021/jm0256124
BindingDB Entry DOI: 10.7270/Q20V8C52
More data for this
Ligand-Target Pair
Monoamine Oxidase Type A (MAO-A)


(Bos taurus)
BDBM15608
PNG
(CHEMBL353159 | N-Methyl,N-propargyl-1H-pyrrole-2-c...)
Show SMILES CN(CC#C)C(=O)c1ccc[nH]1
Show InChI InChI=1S/C9H10N2O/c1-3-7-11(2)9(12)8-5-4-6-10-8/h1,4-6,10H,7H2,2H3
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75n/an/an/an/an/an/an/an/a



Universita di Roma La Sapienza



Assay Description
MAO A and MAO B activities were determined spectrophotometrically using kinuramine as substrates. Fluorimetric measurements were recorded with a Perk...


J Med Chem 50: 922-31 (2007)


Article DOI: 10.1021/jm060882y
BindingDB Entry DOI: 10.7270/Q2GH9G61
More data for this
Ligand-Target Pair
Monoamine Oxidase Type B (MAO-B)


(Bos taurus)
BDBM15608
PNG
(CHEMBL353159 | N-Methyl,N-propargyl-1H-pyrrole-2-c...)
Show SMILES CN(CC#C)C(=O)c1ccc[nH]1
Show InChI InChI=1S/C9H10N2O/c1-3-7-11(2)9(12)8-5-4-6-10-8/h1,4-6,10H,7H2,2H3
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5.00E+4n/an/an/an/an/an/an/an/a



Universita di Roma La Sapienza



Assay Description
MAO A and MAO B activities were determined spectrophotometrically using kinuramine as substrates. Fluorimetric measurements were recorded with a Perk...


J Med Chem 50: 922-31 (2007)


Article DOI: 10.1021/jm060882y
BindingDB Entry DOI: 10.7270/Q2GH9G61
More data for this
Ligand-Target Pair
Monoamine oxidase


(Bos taurus)
BDBM15608
PNG
(CHEMBL353159 | N-Methyl,N-propargyl-1H-pyrrole-2-c...)
Show SMILES CN(CC#C)C(=O)c1ccc[nH]1
Show InChI InChI=1S/C9H10N2O/c1-3-7-11(2)9(12)8-5-4-6-10-8/h1,4-6,10H,7H2,2H3
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5.00E+4n/an/an/an/an/an/an/an/a



Università degli Studi di Roma La Sapienza

Curated by ChEMBL


Assay Description
Inhibitory activity against monoamine oxidase B in isolated bovine brain mitochondria


J Med Chem 46: 917-20 (2003)


Article DOI: 10.1021/jm0256124
BindingDB Entry DOI: 10.7270/Q20V8C52
More data for this
Ligand-Target Pair
Amine oxidase (flavin-containing) A


(Homo sapiens (Human))
BDBM15608
PNG
(CHEMBL353159 | N-Methyl,N-propargyl-1H-pyrrole-2-c...)
Show SMILES CN(CC#C)C(=O)c1ccc[nH]1
Show InChI InChI=1S/C9H10N2O/c1-3-7-11(2)9(12)8-5-4-6-10-8/h1,4-6,10H,7H2,2H3
PDB

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UniProtKB/TrEMBL

antibodypedia
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7.50E+7n/an/an/an/an/an/an/an/a



Bharati Vidyapeeth Deemed University

Curated by ChEMBL


Assay Description
Inhibition of MAO-A receptor


Bioorg Med Chem Lett 21: 2419-24 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.072
BindingDB Entry DOI: 10.7270/Q2QZ2C6S
More data for this
Ligand-Target Pair