Compile Data Set for Download or QSAR
Found 94 with Last Name = 'tiwari' and Initial = 's'
TargetAurora kinase A(Homo sapiens (Human))TBA
LigandPNGBDBM50004205(MK-045 | MK-0457 | TOZASERTIB | US9249124, VX680 |...)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase B(Homo sapiens (Human))TBA
LigandPNGBDBM50600442(CHEMBL5200042)copy SMILES
Affinity DataIC50: 12nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase A(Homo sapiens (Human))TBA
LigandPNGBDBM50600442(CHEMBL5200042)copy SMILES
Affinity DataIC50: 15nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase B(Homo sapiens (Human))TBA
LigandPNGBDBM50600441(CHEMBL5180210)copy SMILES
Affinity DataIC50: 15nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase B(Homo sapiens (Human))TBA
LigandPNGBDBM50004205(MK-045 | MK-0457 | TOZASERTIB | US9249124, VX680 |...)copy SMILEScopy InChI
Affinity DataIC50: 19nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase B(Homo sapiens (Human))TBA
LigandPNGBDBM50600443(CHEMBL5173220)copy SMILES
Affinity DataIC50: 22nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase A(Homo sapiens (Human))TBA
LigandPNGBDBM50600441(CHEMBL5180210)copy SMILES
Affinity DataIC50: 33nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAurora kinase A(Homo sapiens (Human))TBA
LigandPNGBDBM50600443(CHEMBL5173220)copy SMILES
Affinity DataIC50: 42nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3XDTPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
TargetTrypsin(Homo sapiens (Human))
Tel-Aviv University

Curated by ChEMBL
LigandPNGBDBM50491950(CHEMBL2386692)copy SMILEScopy InChI
Affinity DataIC50: 821nMAssay Description:Inhibition of trypsin (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X069ZJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567300(CHEMBL4866457)copy SMILES
Affinity DataIC50: 840nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM22984((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...)copy SMILEScopy InChI
Affinity DataIC50: 940nMAssay Description:Inhibition of human DNA topoisomerase 2 catalytic activity using supercoiled pRYG DNA as substrate measured after 45 mins in presence of ATP by agaro...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ07CRPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567299(CHEMBL4869703)copy SMILES
Affinity DataIC50: 960nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM50543963(CHEMBL4636680)copy SMILEScopy InChI
Affinity DataIC50: 980nMAssay Description:Inhibition of human DNA topoisomerase 2 catalytic activity using supercoiled pRYG DNA as substrate measured after 45 mins in presence of ATP by agaro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ07CRPubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM22984((8S,10S)-10-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-me...)copy SMILEScopy InChI
Affinity DataIC50: 990nMAssay Description:Inhibition of human topoisomerase-2 alpha in human A498 cells assessed as decrease in relaxation of supercoiled DNA at 10 uMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ36GHPubMed
TargetC-C chemokine receptor type 5(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50242053(6,8-didec-(1Z)-enyl-5,7-dimethyl-2,3-dihydro-1H-in...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Displacement of [125I]gp-120 from human CCR5 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29Z94P3PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567299(CHEMBL4869703)copy SMILES
Affinity DataIC50: 1.23E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567300(CHEMBL4866457)copy SMILES
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567298(CHEMBL4854322)copy SMILES
Affinity DataIC50: 1.42E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM50543962(CHEMBL4642846)copy SMILEScopy InChI
Affinity DataIC50: 1.77E+3nMAssay Description:Inhibition of human DNA topoisomerase 2 catalytic activity using supercoiled pRYG DNA as substrate measured after 45 mins in presence of ATP by agaro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ07CRPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 2.16E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567296(CHEMBL4848548)copy SMILES
Affinity DataIC50: 2.41E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetTrypsin(Homo sapiens (Human))
Tel-Aviv University

Curated by ChEMBL
LigandPNGBDBM50491951(CHEMBL2386691)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of trypsin (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X069ZJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567298(CHEMBL4854322)copy SMILES
Affinity DataIC50: 3.14E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetTrypsin(Homo sapiens (Human))
Tel-Aviv University

Curated by ChEMBL
LigandPNGBDBM50491948(CHEMBL2386693)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of trypsin (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X069ZJPubMed
TargetTrypsin(Homo sapiens (Human))
Tel-Aviv University

Curated by ChEMBL
LigandPNGBDBM50491949(CHEMBL2386694)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of trypsin (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X069ZJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567297(CHEMBL4856181)copy SMILES
Affinity DataIC50: 5.32E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50564501(CHEMBL4799941)copy SMILES
Affinity DataIC50: 5.74E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567297(CHEMBL4856181)copy SMILES
Affinity DataIC50: 7.13E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM50543960(CHEMBL4633308)copy SMILEScopy InChI
Affinity DataIC50: 8.15E+3nMAssay Description:Inhibition of human DNA topoisomerase 2 catalytic activity using supercoiled pRYG DNA as substrate measured after 45 mins in presence of ATP by agaro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ07CRPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50564504(CHEMBL4785400)copy SMILES
Affinity DataIC50: 9.91E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM50570427(CHEMBL4864715)copy SMILES
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of human topoisomerase-2 alpha in human A498 cells assessed as decrease in relaxation of supercoiled DNA at 10 uMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ36GHPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567296(CHEMBL4848548)copy SMILES
Affinity DataIC50: 1.13E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM50543961(CHEMBL4647427)copy SMILEScopy InChI
Affinity DataIC50: 1.21E+4nMAssay Description:Inhibition of human DNA topoisomerase 2 catalytic activity using supercoiled pRYG DNA as substrate measured after 45 mins in presence of ATP by agaro...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ07CRPubMed
TargetDNA topoisomerase 2-alpha(Homo sapiens (Human))
Prof John Barnabas Post Graduate School of Biological Studies

Curated by ChEMBL
LigandPNGBDBM50570429(CHEMBL4878037)copy SMILES
Affinity DataIC50: 1.24E+4nMAssay Description:Inhibition of human topoisomerase-2 alpha in human A498 cells assessed as decrease in relaxation of supercoiled DNA at 10 uMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ36GHPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567293(CHEMBL4873165)copy SMILES
Affinity DataIC50: 1.31E+4nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567289(CHEMBL4848801)copy SMILES
Affinity DataIC50: 1.33E+4nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567293(CHEMBL4873165)copy SMILES
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50564501(CHEMBL4799941)copy SMILES
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567294(CHEMBL4864801)copy SMILES
Affinity DataIC50: 1.45E+4nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567310(CHEMBL4863669)copy SMILES
Affinity DataIC50: 1.46E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567302(CHEMBL4871018)copy SMILES
Affinity DataIC50: 1.47E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567308(CHEMBL4865179)copy SMILES
Affinity DataIC50: 1.47E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567295(CHEMBL4860467)copy SMILES
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567303(CHEMBL4876437)copy SMILES
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567292(CHEMBL4868234)copy SMILES
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567294(CHEMBL4864801)copy SMILES
Affinity DataIC50: 1.49E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567307(CHEMBL4863005)copy SMILES
Affinity DataIC50: 1.49E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567301(CHEMBL4860607)copy SMILES
Affinity DataIC50: 1.51E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567290(CHEMBL4851290)copy SMILES
Affinity DataIC50: 1.52E+4nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
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