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BDBM50131526 (R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido)-N-hydroxy-2-(4-(2-(methylamino)ethoxy)phenyl)acetamide::(R)-2-[(4-But-2-ynyloxy-benzenesulfonyl)-methyl-amino]-N-hydroxy-2-[4-(2-methylamino-ethoxy)-phenyl]-acetamide::CHEMBL98061

SMILES: CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO

InChI Key: InChIKey=QCHHXEMLMRDLDA-OAQYLSRUSA-N

Data: 6 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 6 hits for monomerid = 50131526   
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
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50131526
PNG
((R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido...)
Show SMILES CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO
Show InChI InChI=1S/C22H27N3O6S/c1-4-5-15-30-19-10-12-20(13-11-19)32(28,29)25(3)21(22(26)24-27)17-6-8-18(9-7-17)31-16-14-23-2/h6-13,21,23,27H,14-16H2,1-3H3,(H,24,26)/t21-/m1/s1
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n/an/a 11n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibition of Matrix metalloprotein-9


Bioorg Med Chem Lett 13: 2799-803 (2003)


BindingDB Entry DOI: 10.7270/Q21N80H7
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50131526
PNG
((R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido...)
Show SMILES CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO
Show InChI InChI=1S/C22H27N3O6S/c1-4-5-15-30-19-10-12-20(13-11-19)32(28,29)25(3)21(22(26)24-27)17-6-8-18(9-7-17)31-16-14-23-2/h6-13,21,23,27H,14-16H2,1-3H3,(H,24,26)/t21-/m1/s1
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n/an/a 927n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibition of Matrix metalloprotein 1


Bioorg Med Chem Lett 13: 2799-803 (2003)


BindingDB Entry DOI: 10.7270/Q21N80H7
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50131526
PNG
((R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido...)
Show SMILES CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO
Show InChI InChI=1S/C22H27N3O6S/c1-4-5-15-30-19-10-12-20(13-11-19)32(28,29)25(3)21(22(26)24-27)17-6-8-18(9-7-17)31-16-14-23-2/h6-13,21,23,27H,14-16H2,1-3H3,(H,24,26)/t21-/m1/s1
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n/an/a 11n/an/an/an/an/an/a



Pomona College

Curated by ChEMBL


Assay Description
Inhibition of MMP9


Bioorg Med Chem 15: 2223-68 (2007)


Article DOI: 10.1016/j.bmc.2007.01.011
BindingDB Entry DOI: 10.7270/Q2571DBD
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50131526
PNG
((R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido...)
Show SMILES CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO
Show InChI InChI=1S/C22H27N3O6S/c1-4-5-15-30-19-10-12-20(13-11-19)32(28,29)25(3)21(22(26)24-27)17-6-8-18(9-7-17)31-16-14-23-2/h6-13,21,23,27H,14-16H2,1-3H3,(H,24,26)/t21-/m1/s1
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n/an/a 27n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibition of Matrix metalloprotein 13


Bioorg Med Chem Lett 13: 2799-803 (2003)


BindingDB Entry DOI: 10.7270/Q21N80H7
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50131526
PNG
((R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido...)
Show SMILES CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO
Show InChI InChI=1S/C22H27N3O6S/c1-4-5-15-30-19-10-12-20(13-11-19)32(28,29)25(3)21(22(26)24-27)17-6-8-18(9-7-17)31-16-14-23-2/h6-13,21,23,27H,14-16H2,1-3H3,(H,24,26)/t21-/m1/s1
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n/an/a 933n/an/an/an/an/an/a



Pomona College

Curated by ChEMBL


Assay Description
Inhibition of MMP1


Bioorg Med Chem 15: 2223-68 (2007)


Article DOI: 10.1016/j.bmc.2007.01.011
BindingDB Entry DOI: 10.7270/Q2571DBD
More data for this
Ligand-Target Pair
Disintegrin and metalloproteinase domain-containing protein 17


(Homo sapiens (Human))
BDBM50131526
PNG
((R)-2-(4-(but-2-ynyloxy)-N-methylphenylsulfonamido...)
Show SMILES CNCCOc1ccc(cc1)[C@@H](N(C)S(=O)(=O)c1ccc(OCC#CC)cc1)C(=O)NO
Show InChI InChI=1S/C22H27N3O6S/c1-4-5-15-30-19-10-12-20(13-11-19)32(28,29)25(3)21(22(26)24-27)17-6-8-18(9-7-17)31-16-14-23-2/h6-13,21,23,27H,14-16H2,1-3H3,(H,24,26)/t21-/m1/s1
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n/an/a 26n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibition of tumor necrosis factor-alpha converting enzyme


Bioorg Med Chem Lett 13: 2799-803 (2003)


BindingDB Entry DOI: 10.7270/Q21N80H7
More data for this
Ligand-Target Pair