Compile Data Set for Download or QSAR
Report error Found 68 Enz. Inhib. hit(s) with all data for entry = 50042765
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 10404BDBM10404(galantamine | (1S,12S,14R)-9-methoxy-4-methyl-11-o...)
Affinity DataIC50: 2.09E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430681BDBM50430681(CHEMBL2332979)
Affinity DataIC50: 3.36E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430652BDBM50430652(CHEMBL2332975)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430680BDBM50430680(CHEMBL2332980)
Affinity DataIC50: 3.99E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430683BDBM50430683(CHEMBL2332977)
Affinity DataIC50: 4.11E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430651BDBM50430651(CHEMBL2332976)
Affinity DataIC50: 5.99E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430668BDBM50430668(CHEMBL2332981)
Affinity DataIC50: 6.42E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430679BDBM50430679(CHEMBL2332545)
Affinity DataIC50: 6.76E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430672BDBM50430672(CHEMBL2332531)
Affinity DataIC50: 6.96E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430670BDBM50430670(CHEMBL2332541)
Affinity DataIC50: 7.92E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430669BDBM50430669(CHEMBL2332540)
Affinity DataIC50: 8.29E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430665BDBM50430665(CHEMBL2332539)
Affinity DataIC50: 8.72E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430674BDBM50430674(CHEMBL2332533)
Affinity DataIC50: 9.09E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430654BDBM50430654(CHEMBL2332550)
Affinity DataIC50: 9.41E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430672BDBM50430672(CHEMBL2332531)
Affinity DataIC50: 9.45E+3nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430662BDBM50430662(CHEMBL2332537)
Affinity DataIC50: 9.76E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430670BDBM50430670(CHEMBL2332541)
Affinity DataIC50: 1.09E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430676BDBM50430676(CHEMBL2332542)
Affinity DataIC50: 1.14E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430675BDBM50430675(CHEMBL2332534)
Affinity DataIC50: 1.17E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430679BDBM50430679(CHEMBL2332545)
Affinity DataIC50: 1.18E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430663BDBM50430663(CHEMBL2332536)
Affinity DataIC50: 1.18E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430653BDBM50430653(CHEMBL2332974)
Affinity DataIC50: 1.19E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430655BDBM50430655(CHEMBL2332549)
Affinity DataIC50: 1.25E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430677BDBM50430677(CHEMBL2332543)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430675BDBM50430675(CHEMBL2332534)
Affinity DataIC50: 1.36E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430657BDBM50430657(CHEMBL2332547)
Affinity DataIC50: 1.38E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430658BDBM50430658(CHEMBL350032)
Affinity DataIC50: 1.51E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430661BDBM50430661(CHEMBL2332546)
Affinity DataIC50: 1.58E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430654BDBM50430654(CHEMBL2332550)
Affinity DataIC50: 1.59E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430656BDBM50430656(CHEMBL2332548)
Affinity DataIC50: 1.63E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430664BDBM50430664(CHEMBL2332535)
Affinity DataIC50: 1.63E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430666BDBM50430666(CHEMBL2332538)
Affinity DataIC50: 1.74E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430656BDBM50430656(CHEMBL2332548)
Affinity DataIC50: 1.75E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430667BDBM50430667(CHEMBL156016)
Affinity DataIC50: 1.77E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430655BDBM50430655(CHEMBL2332549)
Affinity DataIC50: 1.78E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430671BDBM50430671(CHEMBL2332530)
Affinity DataIC50: 1.79E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430660BDBM50430660(CHEMBL454594)
Affinity DataIC50: 1.81E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430651BDBM50430651(CHEMBL2332976)
Affinity DataIC50: 1.81E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430678BDBM50430678(CHEMBL2332544)
Affinity DataIC50: 1.82E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430676BDBM50430676(CHEMBL2332542)
Affinity DataIC50: 1.92E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 10404BDBM10404(galantamine | (1S,12S,14R)-9-methoxy-4-methyl-11-o...)
Affinity DataIC50: 1.93E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430671BDBM50430671(CHEMBL2332530)
Affinity DataIC50: 1.96E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430678BDBM50430678(CHEMBL2332544)
Affinity DataIC50: 1.97E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430653BDBM50430653(CHEMBL2332974)
Affinity DataIC50: 1.97E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430680BDBM50430680(CHEMBL2332980)
Affinity DataIC50: 1.98E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430682BDBM50430682(CHEMBL2332978)
Affinity DataIC50: 2.01E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430668BDBM50430668(CHEMBL2332981)
Affinity DataIC50: 2.06E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430683BDBM50430683(CHEMBL2332977)
Affinity DataIC50: 2.12E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430659BDBM50430659(CHEMBL152675)
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Universiti Sains Malaysia

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50430667BDBM50430667(CHEMBL156016)
Affinity DataIC50: 2.21E+4nMAssay Description:Inhibition of equine serum BuChE using S-butyrylthiocholine chloride substrate by Ellman's method based spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/24/2013
Entry Details Article
PubMed
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