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PubMed code 11563922

Compile data set for download or QSAR
Found 147 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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40n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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40n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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50n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibition of matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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50n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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60n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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60n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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80n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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80n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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80n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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80n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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90n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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90n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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90n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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100n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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110n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104712
PNG
((S)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m0/s1
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110n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104722
PNG
((S)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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110n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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120n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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130n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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130n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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140n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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140n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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150n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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150n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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150n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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150n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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160n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104722
PNG
((S)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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160n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104712
PNG
((S)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m0/s1
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160n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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170n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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170n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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180n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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180n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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180n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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180n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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180n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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180n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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190n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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190n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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200n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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200n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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200n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104719
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m0/s1
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200n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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200n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibition of matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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220n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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220n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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230n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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240n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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240n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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240n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibition of matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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240n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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240n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibition of matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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250n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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250n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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260n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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260n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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260n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104722
PNG
((S)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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270n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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280n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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280n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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290n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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290n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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300n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104713
PNG
((S)-N-(5-(4-nitrophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES CC(NS(=O)(=O)c1ccccc1)C(=O)NC1=N[N-][C+](CS1)c1ccc(cc1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H17N5O5S2/c1-12(22-30(27,28)15-5-3-2-4-6-15)17(24)19-18-21-20-16(11-29-18)13-7-9-14(10-8-13)23(25)26/h2-10,12,22H,11H2,1H3,(H,19,21,24)
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300n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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300n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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300n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104712
PNG
((S)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m0/s1
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300n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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320n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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320n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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320n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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320n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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330n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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330n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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340n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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340n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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340n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104722
PNG
((S)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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340n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibition of matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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350n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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350n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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350n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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360n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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360n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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360n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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370n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104722
PNG
((S)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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370n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104719
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m0/s1
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380n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104712
PNG
((S)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m0/s1
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380n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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390n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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390n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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390n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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400n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104709
PNG
((R)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m1/s1
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400n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104707
PNG
((S)-N-(5-(4-cyanophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C#N |c:18,t:16|
Show InChI InChI=1S/C19H17N5O3S2/c1-13(24-29(26,27)16-5-3-2-4-6-16)18(25)21-19-23-22-17(12-28-19)15-9-7-14(11-20)8-10-15/h2-10,13,24H,12H2,1H3,(H,21,23,25)/t13-/m0/s1
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400n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the ectodomain of the human matrix metalloproteinase-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104705
PNG
((S)-N-(5-Adamantan-1-yl-6H-[1,3,4]thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)C12CC3CC(CC(C3)C1)C2 |r,c:18,t:16,TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21|
Show InChI InChI=1S/C22H28N4O3S2/c1-14(26-31(28,29)18-5-3-2-4-6-18)20(27)23-21-25-24-19(13-30-21)22-10-15-7-16(11-22)9-17(8-15)12-22/h2-6,14-17,26H,7-13H2,1H3,(H,23,25,27)/t14-,15?,16?,17?,22?/m0/s1
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410n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104712
PNG
((S)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m0/s1
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410n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104718
PNG
((R)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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420n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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430n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104722
PNG
((S)-N-(5-(4-bromophenyl)-6H-1,3,4-thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Br)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17BrN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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440n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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440n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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440n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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440n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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450n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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450n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104716
PNG
((R)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m1/s1
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460n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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470n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104723
PNG
(2-Benzenesulfonylamino-N-[5-(4-chloro-phenyl)-6H-[...)
Show SMILES CC(C)(NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-19(2,24-29(26,27)15-6-4-3-5-7-15)17(25)21-18-23-22-16(12-28-18)13-8-10-14(20)11-9-13/h3-11,24H,12H2,1-2H3,(H,21,23,25)
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480n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104706
PNG
(CHEMBL111179 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)Cc1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:19,t:17|
Show InChI InChI=1S/C19H19ClN4O3S2/c1-13(24-29(26,27)12-14-5-3-2-4-6-14)18(25)21-19-23-22-17(11-28-19)15-7-9-16(20)10-8-15/h2-10,13,24H,11-12H2,1H3,(H,21,23,25)/t13-/m0/s1
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480n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104710
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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500n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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520n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Macrophage metalloelastase


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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520n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-12


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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550n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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550n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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570n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104715
PNG
((S)-2-(phenylsulfonamido)-N-(5-(4-(trifluoromethyl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(cc1)C(F)(F)F |c:18,t:16|
Show InChI InChI=1S/C19H17F3N4O3S2/c1-12(26-31(28,29)15-5-3-2-4-6-15)17(27)23-18-25-24-16(11-30-18)13-7-9-14(10-8-13)19(20,21)22/h2-10,12,26H,11H2,1H3,(H,23,25,27)/t12-/m0/s1
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580n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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580n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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590n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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590n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104712
PNG
((S)-2-(phenylsulfonamido)-N-(5-p-tolyl-6H-1,3,4-th...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(C)cc1 |c:18,t:16|
Show InChI InChI=1S/C19H20N4O3S2/c1-13-8-10-15(11-9-13)17-12-27-19(22-21-17)20-18(24)14(2)23-28(25,26)16-6-4-3-5-7-16/h3-11,14,23H,12H2,1-2H3,(H,20,22,24)/t14-/m0/s1
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620n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104717
PNG
((R)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m1/s1
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630n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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650n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104704
PNG
((S)-N-(5-(4-fluorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(F)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17FN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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650n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104721
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:18,t:16|
Show InChI InChI=1S/C18H17ClN4O3S2/c1-12(23-28(25,26)15-5-3-2-4-6-15)17(24)20-18-22-21-16(11-27-18)13-7-9-14(19)10-8-13/h2-10,12,23H,11H2,1H3,(H,20,22,24)/t12-/m0/s1
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730n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104719
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m0/s1
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740n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104719
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m0/s1
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780n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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800n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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850n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104719
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m0/s1
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880n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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1.04E+3n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-1


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104708
PNG
((S)-N-(5-(4-methoxyphenyl)-6H-1,3,4-thiadiazin-2-y...)
Show SMILES COc1ccc(cc1)C1=NN=C(NC(=O)[C@H](C)NS(=O)(=O)c2ccccc2)SC1 |t:9,11|
Show InChI InChI=1S/C19H20N4O4S2/c1-13(23-29(25,26)16-6-4-3-5-7-16)18(24)20-19-22-21-17(12-28-19)14-8-10-15(27-2)11-9-14/h3-11,13,23H,12H2,1-2H3,(H,20,22,24)/t13-/m0/s1
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1.33E+3n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104711
PNG
(2-Benzenesulfonylamino-N-[5-(5-chloro-thiophen-2-y...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)s1 |c:18,t:16|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)11-5-3-2-4-6-11)15(22)18-16-20-19-12(9-25-16)13-7-8-14(17)26-13/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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1.87E+3n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-14


(Homo sapiens (Human))
BDBM50104705
PNG
((S)-N-(5-Adamantan-1-yl-6H-[1,3,4]thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)C12CC3CC(CC(C3)C1)C2 |r,c:18,t:16,TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21|
Show InChI InChI=1S/C22H28N4O3S2/c1-14(26-31(28,29)18-5-3-2-4-6-18)20(27)23-21-25-24-19(13-30-21)22-10-15-7-16(11-22)9-17(8-15)12-22/h2-6,14-17,26H,7-13H2,1H3,(H,23,25,27)/t14-,15?,16?,17?,22?/m0/s1
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3.07E+3n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of human matrix metalloprotease-14


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104714
PNG
(CHEMBL109861 | N-[5-(4-Chloro-phenyl)-6H-[1,3,4]th...)
Show SMILES C[C@H](NS(=O)(=O)c1cccs1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:17,t:15|
Show InChI InChI=1S/C16H15ClN4O3S3/c1-10(21-27(23,24)14-3-2-8-25-14)15(22)18-16-20-19-13(9-26-16)11-4-6-12(17)7-5-11/h2-8,10,21H,9H2,1H3,(H,18,20,22)/t10-/m0/s1
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3.81E+3n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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4.37E+3n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104705
PNG
((S)-N-(5-Adamantan-1-yl-6H-[1,3,4]thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)C12CC3CC(CC(C3)C1)C2 |r,c:18,t:16,TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21|
Show InChI InChI=1S/C22H28N4O3S2/c1-14(26-31(28,29)18-5-3-2-4-6-18)20(27)23-21-25-24-19(13-30-21)22-10-15-7-16(11-22)9-17(8-15)12-22/h2-6,14-17,26H,7-13H2,1H3,(H,23,25,27)/t14-,15?,16?,17?,22?/m0/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50104705
PNG
((S)-N-(5-Adamantan-1-yl-6H-[1,3,4]thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)C12CC3CC(CC(C3)C1)C2 |r,c:18,t:16,TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21|
Show InChI InChI=1S/C22H28N4O3S2/c1-14(26-31(28,29)18-5-3-2-4-6-18)20(27)23-21-25-24-19(13-30-21)22-10-15-7-16(11-22)9-17(8-15)12-22/h2-6,14-17,26H,7-13H2,1H3,(H,23,25,27)/t14-,15?,16?,17?,22?/m0/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against the catalytic domain of the human matrix metalloprotease-2


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Neutrophil collagenase


(Homo sapiens (Human))
BDBM50104705
PNG
((S)-N-(5-Adamantan-1-yl-6H-[1,3,4]thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)C12CC3CC(CC(C3)C1)C2 |r,c:18,t:16,TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21|
Show InChI InChI=1S/C22H28N4O3S2/c1-14(26-31(28,29)18-5-3-2-4-6-18)20(27)23-21-25-24-19(13-30-21)22-10-15-7-16(11-22)9-17(8-15)12-22/h2-6,14-17,26H,7-13H2,1H3,(H,23,25,27)/t14-,15?,16?,17?,22?/m0/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
Inhibitory activity against matrix metalloprotease-8


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104720
PNG
((R)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m1/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Collagenase 3


(Homo sapiens (Human))
BDBM50104719
PNG
((S)-N-(5-(4-chlorophenyl)-6H-1,3,4-thiadiazin-2-yl...)
Show SMILES CC(C)[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)c1ccc(Cl)cc1 |c:20,t:18|
Show InChI InChI=1S/C20H21ClN4O3S2/c1-13(2)18(25-30(27,28)16-6-4-3-5-7-16)19(26)22-20-24-23-17(12-29-20)14-8-10-15(21)11-9-14/h3-11,13,18,25H,12H2,1-2H3,(H,22,24,26)/t18-/m0/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In Vitro inhibitory activity against the catalytic domain of the matrix metalloprotease-13


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50104705
PNG
((S)-N-(5-Adamantan-1-yl-6H-[1,3,4]thiadiazin-2-yl)...)
Show SMILES C[C@H](NS(=O)(=O)c1ccccc1)C(=O)NC1=NN=C(CS1)C12CC3CC(CC(C3)C1)C2 |r,c:18,t:16,TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21|
Show InChI InChI=1S/C22H28N4O3S2/c1-14(26-31(28,29)18-5-3-2-4-6-18)20(27)23-21-25-24-19(13-30-21)22-10-15-7-16(11-22)9-17(8-15)12-22/h2-6,14-17,26H,7-13H2,1H3,(H,23,25,27)/t14-,15?,16?,17?,22?/m0/s1
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>1.50E+4n/an/an/an/an/an/an/an/a



Universität Bielefeld

Curated by ChEMBL


Assay Description
In vitro inhibition of human matrix metalloprotease-9


J Med Chem 44: 3231-43 (2001)


BindingDB Entry DOI: 10.7270/Q2RN3758
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%