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Found 30 with Last Name = 'anayaba' and Initial = 'j'
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50199883(3,4‐Dichloroisocoumarin (2) | 3,4-Dichloro-i...)
Affinity DataIC50:  100nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281090((3S,4R)-1-Acetyl-3-methoxy-4-phenyl-azetidin-2-one...)
Affinity DataIC50:  400nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281089((3S,4R)-1-Acetyl-3-methoxy-4-((E)-1-methyl-2-pheny...)
Affinity DataIC50:  500nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281090((3S,4R)-1-Acetyl-3-methoxy-4-phenyl-azetidin-2-one...)
Affinity DataIC50:  700nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50199883(3,4‐Dichloroisocoumarin (2) | 3,4-Dichloro-i...)
Affinity DataIC50:  700nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50199883(3,4‐Dichloroisocoumarin (2) | 3,4-Dichloro-i...)
Affinity DataIC50:  800nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281089((3S,4R)-1-Acetyl-3-methoxy-4-((E)-1-methyl-2-pheny...)
Affinity DataIC50:  1.10E+3nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281089((3S,4R)-1-Acetyl-3-methoxy-4-((E)-1-methyl-2-pheny...)
Affinity DataIC50:  1.40E+3nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281090((3S,4R)-1-Acetyl-3-methoxy-4-phenyl-azetidin-2-one...)
Affinity DataIC50:  1.60E+3nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281092((3S,4S)-1,4-Diacetyl-3-methoxy-azetidin-2-one | CH...)
Affinity DataIC50:  1.10E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281093((3S,4S)-3-Butyl-1-[(R)-[1,3]dithian-2-yl-(2,2,2',2...)
Affinity DataIC50:  1.10E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281094((3R,4R)-3-Butyl-1-[(R)-[1,3]dithian-2-yl-(2,2,2',2...)
Affinity DataIC50:  1.30E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281088((3S,4R)-1-[(R)-[1,3]Dithian-2-yl-(2,2,2',2'-tetram...)
Affinity DataIC50:  1.80E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281092((3S,4S)-1,4-Diacetyl-3-methoxy-azetidin-2-one | CH...)
Affinity DataIC50:  2.60E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281086((3S,4S)-1,4-Diacetyl-3-butyl-azetidin-2-one | CHEM...)
Affinity DataIC50:  3.70E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281091((3S,4S)-1-Acetyl-3-butyl-4-((E)-1-methyl-2-phenyl-...)
Affinity DataIC50:  4.30E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281086((3S,4S)-1,4-Diacetyl-3-butyl-azetidin-2-one | CHEM...)
Affinity DataIC50:  4.50E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281091((3S,4S)-1-Acetyl-3-butyl-4-((E)-1-methyl-2-phenyl-...)
Affinity DataIC50:  6.10E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281087((3R,4S)-1-[(R)-[1,3]Dithian-2-yl-(2,2,2',2'-tetram...)
Affinity DataIC50:  7.60E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetNeutrophil elastase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50281092((3S,4S)-1,4-Diacetyl-3-methoxy-azetidin-2-one | CH...)
Affinity DataIC50:  9.40E+4nMAssay Description:The compound was evaluated in vitro for the inhibition of human leukocyte elastase(HLE)More data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281091((3S,4S)-1-Acetyl-3-butyl-4-((E)-1-methyl-2-phenyl-...)
Affinity DataIC50: >1.60E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281086((3S,4S)-1,4-Diacetyl-3-butyl-azetidin-2-one | CHEM...)
Affinity DataIC50: >1.60E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281094((3R,4R)-3-Butyl-1-[(R)-[1,3]dithian-2-yl-(2,2,2',2...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281093((3S,4S)-3-Butyl-1-[(R)-[1,3]dithian-2-yl-(2,2,2',2...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281094((3R,4R)-3-Butyl-1-[(R)-[1,3]dithian-2-yl-(2,2,2',2...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281088((3S,4R)-1-[(R)-[1,3]Dithian-2-yl-(2,2,2',2'-tetram...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281093((3S,4S)-3-Butyl-1-[(R)-[1,3]dithian-2-yl-(2,2,2',2...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281088((3S,4R)-1-[(R)-[1,3]Dithian-2-yl-(2,2,2',2'-tetram...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
TargetChymotrypsin-like elastase family member 2A(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50281087((3R,4S)-1-[(R)-[1,3]Dithian-2-yl-(2,2,2',2'-tetram...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of rat leukocyte elastase(RLE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50281087((3R,4S)-1-[(R)-[1,3]Dithian-2-yl-(2,2,2',2'-tetram...)
Affinity DataIC50: >2.00E+5nMAssay Description:The compound was evaluated in vitro for the inhibition of pancreatitic porcine elastase(PPE); Not ActiveMore data for this Ligand-Target Pair
In DepthDetails Article