Compile Data Set for Download or QSAR
Found 150 with Last Name = 'koseki' and Initial = 'j'
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333455((2S,3S,4S,5S)-2-butyl-5-(hydroxymethyl)pyrrolidine...)copy SMILEScopy InChI
Affinity DataKi:  85nMAssay Description:Competitive inhibition of rat intestinal maltase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50242271((2R,3R,4R,5S)-1-(2-hydroxyethyl)-2-(hydroxymethyl)...)copy SMILEScopy InChI
Affinity DataKi:  460nMAssay Description:Competitive inhibition of rat intestinal maltase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333455((2S,3S,4S,5S)-2-butyl-5-(hydroxymethyl)pyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50049730(2-(5-(2-methyl-3-phenylallylidene)-4-oxo-2-thioxot...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333457((2S,3S,4S,5S)-2-hexyl-5-(hydroxymethyl)pyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50263044(CHEMBL476960 | Voglibose)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM18363((2R,3R,4R,5S,6R)-2-(hydroxymethyl)-6-octylpiperidi...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of rat intestinal isomaltase using isomoltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333455((2S,3S,4S,5S)-2-butyl-5-(hydroxymethyl)pyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363064(CHEMBL1944855)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363053(CHEMBL1944862)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333465((2R,3R,4R,5R,6R)-5-((2R,3R,4R,5S,6R)-5-((2R,3R,4S,...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50399654(CHEMBL2177691)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363063(CHEMBL1944854)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333456((2S,3S,4S,5S)-2-(hydroxymethyl)-5-pentylpyrrolidin...)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363066(CHEMBL1944857)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363070(CHEMBL1944861)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363065(CHEMBL1944856)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50399655(CHEMBL2177690)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363054(CHEMBL1946959)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363055(CHEMBL1946960)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363061(CHEMBL1946966)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50399654(CHEMBL2177691)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333458((2S,3S,4S,5S)-2-heptyl-5-(hydroxymethyl)pyrrolidin...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333454((2S,3S,4S,5S)-2-(hydroxymethyl)-5-propylpyrrolidin...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363057(CHEMBL1946962)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Inhibition of rat intestinal isomaltase using isomoltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM18362((2R,3S,4R,5R,6R)-2-hexyl-6-(hydroxymethyl)piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibition of rat intestinal isomaltase using isomoltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50399655(CHEMBL2177690)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333459((2S,3S,4S,5S)-2-(hydroxymethyl)-5-octylpyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363060(CHEMBL1946965)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50049730(2-(5-(2-methyl-3-phenylallylidene)-4-oxo-2-thioxot...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363062(CHEMBL1944853)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50375511(CHEMBL406973)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Inhibition of rat intestinal isomaltase using isomoltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50263044(CHEMBL476960 | Voglibose)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333458((2S,3S,4S,5S)-2-heptyl-5-(hydroxymethyl)pyrrolidin...)copy SMILEScopy InChI
Affinity DataIC50: 380nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363069(CHEMBL1944860)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333459((2S,3S,4S,5S)-2-(hydroxymethyl)-5-octylpyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM18361((2R,3S,4R,5R,6R)-2-butyl-6-(hydroxymethyl)piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:Inhibition of rat intestinal isomaltase using isomoltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363067(CHEMBL1944858)copy SMILEScopy InChI
Affinity DataIC50: 480nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333457((2S,3S,4S,5S)-2-hexyl-5-(hydroxymethyl)pyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 510nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50375510(CHEMBL405957)copy SMILEScopy InChI
Affinity DataIC50: 620nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50399650(CHEMBL2177689)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50399653(CHEMBL2177692)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333453((2S,3S,4S,5S)-2-ethyl-5-(hydroxymethyl)pyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of rat intestinal sucrase using sucrose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363072(CHEMBL1944852)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333456((2S,3S,4S,5S)-2-(hydroxymethyl)-5-pentylpyrrolidin...)copy SMILEScopy InChI
Affinity DataIC50: 710nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50375510(CHEMBL405957)copy SMILEScopy InChI
Affinity DataIC50: 770nMAssay Description:Inhibition of rat intestinal isomaltase using isomoltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
TargetLysosomal alpha-glucosidase(Rattus norvegicus)
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50333461((2S,3S,4S,5S)-2-(hydroxymethyl)-5-nonylpyrrolidine...)copy SMILEScopy InChI
Affinity DataIC50: 840nMAssay Description:Inhibition of rat intestinal maltase using moltose as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VTXPubMed
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