Compile Data Set for Download or QSAR
Report error Found 228 Enz. Inhib. hit(s) with all data for entry = 50010513
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095584BDBM50095584(4-(2-Benzyloxy-3-phenyl-propionylamino)-1-(4-metho...)
Affinity DataIC50: 0.200nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095576BDBM50095576(1-(4-Butoxy-benzenesulfonyl)-4-(2,5-dioxo-3-propyl...)
Affinity DataIC50: 0.300nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095581BDBM50095581(4-(2-Benzyloxy-propionylamino)-1-(4-methoxy-benzen...)
Affinity DataIC50: 0.300nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095573BDBM50095573(4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-(4-prop...)
Affinity DataIC50: 0.300nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095538BDBM50095538(1-(4-Butoxy-benzenesulfonyl)-4-(3-methyl-2,5-dioxo...)
Affinity DataIC50: 0.300nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095554BDBM50095554(4-(1,1-Dioxo-1lambda*6*-isothiazolidin-2-yl)-1-(4-...)
Affinity DataIC50: 0.400nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095576BDBM50095576(1-(4-Butoxy-benzenesulfonyl)-4-(2,5-dioxo-3-propyl...)
Affinity DataIC50: 0.400nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095546BDBM50095546(4-Piperidin-1-yl-1-(4-propoxy-benzenesulfonyl)-pyr...)
Affinity DataIC50: 0.400nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095558BDBM50095558(4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-(4-propo...)
Affinity DataIC50: 0.400nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095560BDBM50095560(4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-(4-butox...)
Affinity DataIC50: 0.400nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095580BDBM50095580(4-(Methanesulfonyl-methyl-amino)-1-(4-methoxy-benz...)
Affinity DataIC50: 0.5nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095579BDBM50095579(1-(4-Methoxy-benzenesulfonyl)-4-(3-methyl-2,5-diox...)
Affinity DataIC50: 0.5nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095540BDBM50095540(4-[(2-Hydroxy-4-phenyl-butyryl)-propyl-amino]-1-(4...)
Affinity DataIC50: 0.5nMAssay Description:Inhibition of matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095541BDBM50095541(1-(4-Butoxy-benzenesulfonyl)-4-morpholin-4-yl-pyrr...)
Affinity DataIC50: 0.600nMAssay Description:Inhibition of matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095540BDBM50095540(4-[(2-Hydroxy-4-phenyl-butyryl)-propyl-amino]-1-(4...)
Affinity DataIC50: 0.600nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095593BDBM50095593(1-(4-Butoxy-benzenesulfonyl)-4-(2-methoxy-acetylam...)
Affinity DataIC50: 0.700nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095567BDBM50095567(1-(4-Butoxy-benzenesulfonyl)-4-methanesulfonylamin...)
Affinity DataIC50: 0.700nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095547BDBM50095547(4-[(2-Hydroxy-propionyl)-propyl-amino]-1-(4-methox...)
Affinity DataIC50: 0.700nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095570BDBM50095570(4-(3-Methyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(pyr...)
Affinity DataIC50: 0.700nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095578BDBM50095578(4-Morpholin-4-yl-1-(4-pentyl-benzenesulfonyl)-pyrr...)
Affinity DataIC50: 0.700nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095558BDBM50095558(4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-(4-propo...)
Affinity DataIC50: 0.800nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095569BDBM50095569(4-(Methanesulfonyl-propyl-amino)-1-(4-methoxy-benz...)
Affinity DataIC50: 0.800nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095567BDBM50095567(1-(4-Butoxy-benzenesulfonyl)-4-methanesulfonylamin...)
Affinity DataIC50: 0.800nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095592BDBM50095592(4-Methanesulfonylamino-1-[4-(pyridin-4-yloxy)-benz...)
Affinity DataIC50: 0.800nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095589BDBM50095589(1-(4-Butoxy-benzenesulfonyl)-4-(2-hydroxy-3-methyl...)
Affinity DataIC50: 0.800nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095569BDBM50095569(4-(Methanesulfonyl-propyl-amino)-1-(4-methoxy-benz...)
Affinity DataIC50: 0.800nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095582BDBM50095582(1-(4-Pentyl-benzenesulfonyl)-4-piperidin-1-yl-pyrr...)
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095590BDBM50095590(1-(4-Butoxy-benzenesulfonyl)-4-(2-hydroxy-4-methyl...)
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095562BDBM50095562(1-(4-Butoxy-benzenesulfonyl)-4-(1,1-dioxo-1lambda*...)
Affinity DataIC50: 0.900nMAssay Description:Inhibition of matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095568BDBM50095568(1-(4-Butoxy-benzenesulfonyl)-4-(2-hydroxy-propiony...)
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095542BDBM50095542(1-[4-(2-Methoxy-ethoxy)-benzenesulfonyl]-4-(3-meth...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095547BDBM50095547(4-[(2-Hydroxy-propionyl)-propyl-amino]-1-(4-methox...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095543BDBM50095543(1'-(4-Propoxy-benzenesulfonyl)-[1,3']bipyrrolidiny...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095564BDBM50095564(1-(4-Methoxy-benzenesulfonyl)-4-piperidin-1-yl-pyr...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095544BDBM50095544(4-(Methanesulfonyl-pyridin-3-ylmethyl-amino)-1-(4-...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095586BDBM50095586(4-(1,1-Dioxo-1lambda*6*-thiomorpholin-4-yl)-1-(4-m...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095551BDBM50095551(4-(2-Hydroxy-propionylamino)-1-(4-propoxy-benzenes...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095583BDBM50095583(4-Morpholin-4-yl-1-(4-propoxy-benzenesulfonyl)-pyr...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095594BDBM50095594(1-(4-Methoxy-benzenesulfonyl)-4-phenethylamino-pyr...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095594BDBM50095594(1-(4-Methoxy-benzenesulfonyl)-4-phenethylamino-pyr...)
Affinity DataIC50: 1nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095548BDBM50095548(4-Methanesulfonylamino-1-(4-methoxy-benzenesulfony...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095549BDBM50095549(4-(2,5-Dioxo-3-propyl-imidazolidin-1-yl)-1-[4-(2-m...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095544BDBM50095544(4-(Methanesulfonyl-pyridin-3-ylmethyl-amino)-1-(4-...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095556BDBM50095556(1-(4-Methoxy-benzenesulfonyl)-4-(4-methoxy-benzene...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095555BDBM50095555(4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(2-me...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCollagenase 3(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095548BDBM50095548(4-Methanesulfonylamino-1-(4-methoxy-benzenesulfony...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against human recombinant matrix metalloprotease-13 (collagenase-3)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095585BDBM50095585(1-(4-Butoxy-benzenesulfonyl)-4-(4,4-dimethyl-2,5-d...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095555BDBM50095555(4-(3-Allyl-2,5-dioxo-imidazolidin-1-yl)-1-[4-(2-me...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetStromelysin-1(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095538BDBM50095538(1-(4-Butoxy-benzenesulfonyl)-4-(3-methyl-2,5-dioxo...)
Affinity DataIC50: 2nMAssay Description:Inhibition of matrix metalloprotease-3 (stromelysin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Target72 kDa type IV collagenase(Human)
Procter and Gamble Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50095549BDBM50095549(4-(2,5-Dioxo-3-propyl-imidazolidin-1-yl)-1-[4-(2-m...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibitory activity against matrix metalloprotease -2 (gelatinase-A)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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