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Found 75 with Last Name = 'ayazgok' and Initial = 'b'
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406864(CHEMBL4161244)
Affinity DataKi:  6.91E+3nMAssay Description:Non-competitive inhibition of electric eel AChE using varying levels of acetylthiocholine iodide as substrate pretreated for 5 mins followed by subst...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Hacettepe University

LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  6.16nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  20nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  3.40E+3nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  4.94E+3nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
In DepthDetails
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225274(2-[4-(4-Ethylpiperazin-1-yl)phenyl]-1H-benzo[d]imi...)
Affinity DataIC50:  5.18E+3nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225276(2-[4-(4-Benzylpiperazin-1-yl)phenyl]-1H-benzo[d]im...)
Affinity DataIC50:  5.22E+3nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406848(CHEMBL4160630)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406860(CHEMBL4159985)
Affinity DataIC50:  1.03E+4nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225280(5-Methoxy-2-[4-(4-benzylpiperazin-1-yl)phenyl]-1H-...)
Affinity DataIC50:  1.15E+4nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225273(2-[4-(4-Methylpiperazin-1-yl)phenyl]-1H-benzo[d]im...)
Affinity DataIC50:  1.57E+4nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
In DepthDetails
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406864(CHEMBL4161244)
Affinity DataIC50:  1.64E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225277(5-Methoxy-2-[4-(4-methylpiperazin-1-yl)phenyl]-1H-...)
Affinity DataIC50:  1.78E+4nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225278(5-Methoxy-2-[4-(4-ethylpiperazin-1-yl)phenyl]-1H-b...)
Affinity DataIC50:  2.02E+4nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetAcetylcholinesterase(Homo sapiens (Human))
Hacettepe University

LigandPNGBDBM225274(2-[4-(4-Ethylpiperazin-1-yl)phenyl]-1H-benzo[d]imi...)
Affinity DataIC50:  3.49E+4nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406855(CHEMBL4175303)
Affinity DataIC50:  4.02E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406843(CHEMBL4171854)
Affinity DataIC50:  4.65E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406864(CHEMBL4161244)
Affinity DataIC50:  4.94E+4nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406849(CHEMBL4164474)
Affinity DataIC50:  5.20E+4nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406852(CHEMBL4163570)
Affinity DataIC50:  5.46E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406856(CHEMBL4161751)
Affinity DataIC50:  5.50E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406865(CHEMBL4171465)
Affinity DataIC50:  5.50E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406861(CHEMBL4171674)
Affinity DataIC50:  5.97E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406844(CHEMBL4168105)
Affinity DataIC50:  6.55E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406840(CHEMBL4160205)
Affinity DataIC50:  6.67E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406842(CHEMBL4167902)
Affinity DataIC50:  7.06E+4nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406857(CHEMBL4163548)
Affinity DataIC50:  7.35E+4nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Hacettepe University

LigandPNGBDBM225276(2-[4-(4-Benzylpiperazin-1-yl)phenyl]-1H-benzo[d]im...)
Affinity DataIC50:  9.72E+4nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406850(CHEMBL4159579)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406840(CHEMBL4160205)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406851(CHEMBL4164667)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406841(CHEMBL4171444)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406851(CHEMBL4164667)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406853(CHEMBL4175113)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406854(CHEMBL4176178)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406846(CHEMBL4168331)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406856(CHEMBL4161751)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406847(CHEMBL4161064)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406846(CHEMBL4168331)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406845(CHEMBL4170408)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406844(CHEMBL4168105)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406843(CHEMBL4171854)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406841(CHEMBL4171444)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Hacettepe University

LigandPNGBDBM225279(5-Methoxy-2-[4-(4-phenylpiperazin-1-yl)phenyl]-1H-...)
Affinity DataIC50: >1.00E+5nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetAcetylcholinesterase(Homo sapiens (Human))
Hacettepe University

LigandPNGBDBM225275(2-[4-(4-Phenylpiperazin-1-yl)phenyl]-1H-benzo[d]im...)
Affinity DataIC50: >1.00E+5nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406855(CHEMBL4175303)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225275(2-[4-(4-Phenylpiperazin-1-yl)phenyl]-1H-benzo[d]im...)
Affinity DataIC50: >1.00E+5nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
Hacettepe University

LigandPNGBDBM225279(5-Methoxy-2-[4-(4-phenylpiperazin-1-yl)phenyl]-1H-...)
Affinity DataIC50: >1.00E+5nMpH: 8.0 T: 2°CAssay Description:Reactions were performed in a mediumcontaining substrate (0.05-0.4 mM) combined with 0.125 mM DTNB in 100 mM 3-(N-morpholino)propanesulfonic acid buf...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406866(CHEMBL4169996)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tehran University Of Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50406852(CHEMBL4163570)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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