Compile Data Set for Download or QSAR
Found 73 with Last Name = 'cazzanelli' and Initial = 'g'
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50335638(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564382(CHEMBL4795023)copy SMILES
Affinity DataIC50: 280nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564384(CHEMBL4784643)copy SMILES
Affinity DataIC50: 320nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M330H3PubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564388(CHEMBL4776391)copy SMILES
Affinity DataIC50: 330nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564381(CHEMBL4778120)copy SMILES
Affinity DataIC50: 360nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50252622(CHEMBL4070389)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564387(CHEMBL4789806)copy SMILES
Affinity DataIC50: 370nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M330H3PubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564385(CHEMBL4798710)copy SMILES
Affinity DataIC50: 370nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564383(CHEMBL4783065)copy SMILES
Affinity DataIC50: 710nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M330H3PubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564380(CHEMBL4799521)copy SMILES
Affinity DataIC50: 880nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M330H3PubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564386(CHEMBL4796675)copy SMILES
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M330H3PubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50564379(CHEMBL4792639)copy SMILES
Affinity DataIC50: 1.37E+3nMAssay Description:Inhibition of recombinant human CK2alpha (1 to 336 residues) expressed in Escherichia coli BL21 (DE3) using RRADDSDDDD as substrate incubated for 10 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetSRSF protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50564378(CHEMBL4787157)copy SMILES
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of recombinant human SRPK1 expressed in Escherichia coli using RS peptide as substrate incubated for 15 mins in presence of ATP by Kinase-...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M330H3PubMed
LigandPNGBDBM50601335(CHEMBL5178939)copy SMILES
Affinity DataIC50: 4.00E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601334(CHEMBL5172246)copy SMILES
Affinity DataIC50: 1.06E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601332(CHEMBL5174553)copy SMILES
Affinity DataIC50: 1.09E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601341(CHEMBL5205271)copy SMILES
Affinity DataIC50: 1.10E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601322(CHEMBL5192710)copy SMILES
Affinity DataIC50: 1.10E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601319(CHEMBL5186561)copy SMILES
Affinity DataIC50: 1.14E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601320(CHEMBL5170762)copy SMILES
Affinity DataIC50: 1.18E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601318(CHEMBL5172147)copy SMILES
Affinity DataIC50: 1.25E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601331(CHEMBL5200427)copy SMILES
Affinity DataIC50: 1.26E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601328(CHEMBL5205483)copy SMILES
Affinity DataIC50: 1.29E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601327(CHEMBL5171471)copy SMILES
Affinity DataIC50: 1.31E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601343(CHEMBL5190134)copy SMILES
Affinity DataIC50: 1.40E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601337(CHEMBL5190709)copy SMILES
Affinity DataIC50: 1.41E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601340(CHEMBL5191503)copy SMILES
Affinity DataIC50: 2.20E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601323(CHEMBL5207551)copy SMILES
Affinity DataIC50: 2.92E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601339(CHEMBL5184671)copy SMILES
Affinity DataIC50: 3.13E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601336(CHEMBL5179501)copy SMILES
Affinity DataIC50: 3.32E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601290(CHEMBL5195335)copy SMILES
Affinity DataIC50: 3.32E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601294(CHEMBL5181472)copy SMILES
Affinity DataIC50: 3.33E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601338(CHEMBL5200749)copy SMILES
Affinity DataIC50: 3.51E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601333(CHEMBL5187101)copy SMILES
Affinity DataIC50: 3.65E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601316(CHEMBL5194817)copy SMILES
Affinity DataIC50: 3.89E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601317(CHEMBL5172880)copy SMILES
Affinity DataIC50: 4.01E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601342(CHEMBL5197323)copy SMILES
Affinity DataIC50: 4.20E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601326(CHEMBL5186928)copy SMILES
Affinity DataIC50: 4.29E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601321(CHEMBL5187277)copy SMILES
Affinity DataIC50: 4.46E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601325(CHEMBL5194936)copy SMILES
Affinity DataIC50: 4.66E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601296(CHEMBL5193546)copy SMILES
Affinity DataIC50: 4.70E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601330(CHEMBL5180696)copy SMILES
Affinity DataIC50: 4.93E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601308(CHEMBL5184699)copy SMILES
Affinity DataIC50: 5.39E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601299(CHEMBL5197053)copy SMILES
Affinity DataIC50: 5.40E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601307(CHEMBL5193585)copy SMILES
Affinity DataIC50: 5.40E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601311(CHEMBL5183618)copy SMILES
Affinity DataIC50: 5.40E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601314(CHEMBL5183063)copy SMILES
Affinity DataIC50: 5.46E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
LigandPNGBDBM50601292(CHEMBL5185177)copy SMILES
Affinity DataIC50: 5.79E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601309(CHEMBL5206608)copy SMILES
Affinity DataIC50: 6.05E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
LigandPNGBDBM50601300(CHEMBL5206097)copy SMILES
Affinity DataIC50: 6.13E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27M0D0ZPubMed
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