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SMILES: OP(O)(=O)C(=O)NCCc1ccccc1

InChI Key: InChIKey=GHFCXEYUGIXTHN-UHFFFAOYSA-N

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 11 hits for monomerid = 50112446   
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
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a>5.00E+6n/an/an/an/an/an/a



Aventis Pharma

Curated by ChEMBL


Assay Description
The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domain


Bioorg Med Chem Lett 12: 1295-8 (2002)


BindingDB Entry DOI: 10.7270/Q2959GW0
More data for this
Ligand-Target Pair
Stromelysin-1


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 9.00E+4n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against recombinant matrix metalloprotease-3 was determined


J Med Chem 47: 2826-32 (2004)


Article DOI: 10.1021/jm030386z
BindingDB Entry DOI: 10.7270/Q2XS5W4C
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against recombinant matrix metalloprotease-8 was determined


J Med Chem 47: 2826-32 (2004)


Article DOI: 10.1021/jm030386z
BindingDB Entry DOI: 10.7270/Q2XS5W4C
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against recombinant matrix metalloprotease-9 was determined


J Med Chem 47: 2826-32 (2004)


Article DOI: 10.1021/jm030386z
BindingDB Entry DOI: 10.7270/Q2XS5W4C
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 2.00E+4n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against recombinant matrix metalloprotease-2 was determined


J Med Chem 47: 2826-32 (2004)


Article DOI: 10.1021/jm030386z
BindingDB Entry DOI: 10.7270/Q2XS5W4C
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 2.00E+4n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
Inhibition of MMP2


J Med Chem 55: 7875-82 (2012)


Article DOI: 10.1021/jm300981b
BindingDB Entry DOI: 10.7270/Q23T9JBB
More data for this
Ligand-Target Pair
Carbonic anhydrase 12


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 5.44E+3n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
Inhibition of human Carbonic anhydrase 12-mediated CO2 hydration by stopped-flow method


J Med Chem 55: 7875-82 (2012)


Article DOI: 10.1021/jm300981b
BindingDB Entry DOI: 10.7270/Q23T9JBB
More data for this
Ligand-Target Pair
Carbonic anhydrase 9


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 6.08E+3n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
Inhibition of human Carbonic anhydrase 9-mediated CO2 hydration by stopped-flow method


J Med Chem 55: 7875-82 (2012)


Article DOI: 10.1021/jm300981b
BindingDB Entry DOI: 10.7270/Q23T9JBB
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 8.00E+3n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
Inhibition of human Carbonic anhydrase 2-mediated CO2 hydration by stopped-flow method


J Med Chem 55: 7875-82 (2012)


Article DOI: 10.1021/jm300981b
BindingDB Entry DOI: 10.7270/Q23T9JBB
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 7.68E+3n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
Inhibition of human Carbonic anhydrase 1-mediated CO2 hydration by stopped-flow method


J Med Chem 55: 7875-82 (2012)


Article DOI: 10.1021/jm300981b
BindingDB Entry DOI: 10.7270/Q23T9JBB
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50112446
PNG
(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)
Show SMILES OP(O)(=O)C(=O)NCCc1ccccc1
Show InChI InChI=1S/C9H12NO4P/c11-9(15(12,13)14)10-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)(H2,12,13,14)
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n/an/a 8.00E+4n/an/an/an/an/an/a



The Hebrew University of Jerusalem

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against recombinant matrix metalloprotease-1 was determined


J Med Chem 47: 2826-32 (2004)


Article DOI: 10.1021/jm030386z
BindingDB Entry DOI: 10.7270/Q2XS5W4C
More data for this
Ligand-Target Pair