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TargetSignal transducer and activator of transcription 3(Human)
University of Southern California

Curated by ChEMBL
LigandPNGBDBM50396177(NIFUROXAZIDE)
Affinity DataEC50:  3.00E+3nMAssay Description:Inhibition of STAT3 expressed in human U3A cells after 1 hr by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetSignal transducer and activator of transcription 3(Mouse)
University of Southern California

Curated by ChEMBL
LigandPNGBDBM50353441(CHEMBL1829786)
Affinity DataKd:  2.74E+3nMAssay Description:Binding affinity to STAT3 SH2 in v-Src transformed mouse NIH/3T3 cells overexpressing human EGFRMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090867((2R,3S,4R,5R)-2-(aminomethyl)-5-(4-chloro-5-iodo-7...)
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090843((2R,3R,4S,5R)-2-(4-amino-5-bromo-7H-pyrrolo[2,3-d]...)
Affinity DataIC50: 0.200nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090862((1R,5S)-2-((3R,4aR)-4-Amino-5-iodo-pyrrolo[2,3-d]p...)
Affinity DataIC50: 0.600nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090844(2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 3nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM14486(CHEMBL66280 | 5-Iodo-5-deoxytubercidin | 7-(5-deox...)
Affinity DataIC50: 9nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090854((2R,3S,4R,5R)-2-Azidomethyl-5-(4-chloro-5-iodo-pyr...)
Affinity DataIC50: 9nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567384(CHEMBL4849586)
Affinity DataIC50: 21nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090853(2-(4-Chloro-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 24nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50042349(2-(4-Amino-5-iodo-pyrrolo[2,3-d]pyrimidin-7-yl)-5-...)
Affinity DataIC50: 26nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567363(CHEMBL4876602)
Affinity DataIC50: 34nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090863((2R,3R,4S,5R)-2-(4-amino-5-iodo-7H-pyrrolo[2,3-d]p...)
Affinity DataIC50: 35nMAssay Description:Micromolar concentration required for 50% inhibition of Adenosine Kinase enzyme activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090847(2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 40nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567363(CHEMBL4876602)
Affinity DataIC50: 40nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090855(2-(5-Iodo-4-methylsulfanyl-pyrrolo[2,3-d]pyrimidin...)
Affinity DataIC50: 45nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090852((2R,3R,4S,5R)-2-(5-Bromo-4-chloro-pyrrolo[2,3-d]py...)
Affinity DataIC50: 50nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567386(CHEMBL4861872)
Affinity DataIC50: 50nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50076742(CHEBI:86194 | CHEMBL3416563)
Affinity DataIC50: 57nMAssay Description:Inhibition of human ALDH1A1More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567385(CHEMBL4846203)
Affinity DataIC50: 58nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090864((2R,3R,4S,5R)-2-(4-Amino-5-iodo-pyrrolo[2,3-d]pyri...)
Affinity DataIC50: 60nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567382(CHEMBL4859904)
Affinity DataIC50: 60nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090860(2-(4-Amino-5-bromo-pyrrolo[2,3-d]pyrimidin-7-yl)-5...)
Affinity DataIC50: 63nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567372(CHEMBL4875157)
Affinity DataIC50: 63nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567383(CHEMBL4847114)
Affinity DataIC50: 65nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50567384(CHEMBL4849586)
Affinity DataIC50: 68nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090866(2-(4-Chloro-5-methylsulfanyl-pyrrolo[2,3-d]pyrimid...)
Affinity DataIC50: 70nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50567363(CHEMBL4876602)
Affinity DataIC50: 70nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567362(CHEMBL4848258)
Affinity DataIC50: 73nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50459588(CHEMBL4210115)
Affinity DataIC50: 80nMAssay Description:Inhibition of human recombinant ALDH1A1 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50459603(CHEMBL4213331)
Affinity DataIC50: 80nMAssay Description:Inhibition of human recombinant ALDH1A1 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50459603(CHEMBL4213331)
Affinity DataIC50: 80nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50459588(CHEMBL4210115)
Affinity DataIC50: 80nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567382(CHEMBL4859904)
Affinity DataIC50: 80nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567373(CHEMBL4855442)
Affinity DataIC50: 89nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567372(CHEMBL4875157)
Affinity DataIC50: 89nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50459603(CHEMBL4213331)
Affinity DataIC50: 90nMAssay Description:Inhibition of human recombinant ALDH1A3 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50459603(CHEMBL4213331)
Affinity DataIC50: 90nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567376(CHEMBL4848831)
Affinity DataIC50: 91nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50567386(CHEMBL4861872)
Affinity DataIC50: 93nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50567374(CHEMBL4849624)
Affinity DataIC50: 94nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567373(CHEMBL4855442)
Affinity DataIC50: 95nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50459609(CHEMBL4214000)
Affinity DataIC50: 100nMAssay Description:Inhibition of human recombinant ALDH1A1 assessed as reduction in of NAD(P)H formation incubated for 2 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2020
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090837((2R,3R,4S,5R)-2-(4-amino-5-iodo-7H-pyrrolo[2,3-d]p...)
Affinity DataIC50: 100nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM50090859(2-Azidomethyl-5-(5-bromo-4-chloro-pyrrolo[2,3-d]py...)
Affinity DataIC50: 100nMAssay Description:Inhibition of human adenosine kinase activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50567382(CHEMBL4859904)
Affinity DataIC50: 100nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567376(CHEMBL4848831)
Affinity DataIC50: 100nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase family 1 member A3(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567374(CHEMBL4849624)
Affinity DataIC50: 100nMAssay Description:Inhibition of human ALDH1A3 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetRetinal dehydrogenase 2(Human)
University of Michigan

Curated by ChEMBL
LigandPNGBDBM50567378(CHEMBL4846491)
Affinity DataIC50: 108nMAssay Description:Inhibition of human ALDH1A2 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
TargetAldehyde dehydrogenase 1A1(Human)
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50567383(CHEMBL4847114)
Affinity DataIC50: 109nMAssay Description:Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometeryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2022
Entry Details Article
PubMed
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