Compile Data Set for Download or QSAR
maximum 50k data
Found 56 with Last Name = 'santoriello' and Initial = 'm'
TargetIntegrase(Human immunodeficiency virus 1)
Irbm

Curated by ChEMBL
LigandPNGBDBM25351(N-[2-(4-{[(4-fluorophenyl)methyl]carbamoyl}-5-hydr...)
Affinity DataIC50:  27nMAssay Description:Inhibition of wild type recombinant HIV1 His6-tagged integrase expressed in Escherichia coli BL21 using 18 nucleotide 3'-biotin labeled DNA acceptor ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM8611(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)
Affinity DataIC50:  50nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263871(1-[2-Biphenyl-4-yl-1-(4-fluoro-benzyl)-ethyl]-1H-i...)
Affinity DataIC50:  110nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263761(Biphenyl-4-ylmethyl-(4-fluoro-benzyl)-imidazol-1-y...)
Affinity DataIC50:  190nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263924(1-[2-Biphenyl-4-yl-1-(2,4-difluoro-benzyl)-ethyl]-...)
Affinity DataIC50:  260nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263719(Biphenyl-4-ylmethyl-(2-chloro-benzyl)-imidazol-1-y...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263461(CHEMBL517347 | N-(5-chlorothiophen-2-ylmethyl)-N-(...)
Affinity DataIC50:  320nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263808(Biphenyl-4-ylmethyl-(2,4-difluoro-benzyl)-imidazol...)
Affinity DataIC50:  350nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263720(Biphenyl-4-ylmethyl-(2-fluoro-benzyl)-imidazol-1-y...)
Affinity DataIC50:  460nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263921(1-[2-Biphenyl-4-yl-1-(2-methoxy-benzyl)-ethyl]-1H-...)
Affinity DataIC50:  510nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263810(CHEMBL523973 | N-(4-tert-butylbenzyl)-N-(thiophen-...)
Affinity DataIC50:  580nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263465(1-(5-chlorothiophen-2-yl)-2-(1H-imidazol-1-yl)-3-p...)
Affinity DataIC50:  870nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263812(1-(1-Benzyl-2-biphenyl-4-yl-ethyl)-1H-imidazole | ...)
Affinity DataIC50:  950nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263811(1-[2-Biphenyl-4-yl-1-(4-tert-butyl-benzyl)-ethyl]-...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263343(CHEMBL476979 | N-(1,1'-biphenyl-4-ylmethyl)-N-(5-c...)
Affinity DataIC50:  1.04E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263867(1-[2-Biphenyl-4-yl-1-(2-methyl-benzyl)-ethyl]-1H-i...)
Affinity DataIC50:  1.04E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263368(CHEMBL476143 | N-benzyl-N-(5-chlorothiophen-2-yl-m...)
Affinity DataIC50:  1.06E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263464(1-(1,1'-biphenyl-4-yl)-3-(5-chloro-thiophen-2-yl)-...)
Affinity DataIC50:  1.07E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263868(1-[2-Biphenyl-4-yl-1-(2-chloro-benzyl)-ethyl]-1H-i...)
Affinity DataIC50:  1.09E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263760(Biphenyl-4-ylmethyl-(4-chloro-benzyl)-imidazol-1-y...)
Affinity DataIC50:  1.18E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263717(Benzyl-biphenyl-4-ylmethyl-imidazol-1-yl-amine | C...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263923(1-[2-Biphenyl-4-yl-1-(2,4-dichloro-benzyl)-ethyl]-...)
Affinity DataIC50:  1.24E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263870(1-[2-Biphenyl-4-yl-1-(4-methyl-benzyl)-ethyl]-1H-i...)
Affinity DataIC50:  1.32E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263869(1-[2-Biphenyl-4-yl-1-(2-fluoro-benzyl)-ethyl]-1H-i...)
Affinity DataIC50:  1.37E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263762(Biphenyl-4-ylmethyl-imidazol-1-yl-(2-methoxy-benzy...)
Affinity DataIC50:  1.51E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263809(CHEMBL491825 | N-(2,4-dichlorobenzyl)-N-(4-tert-bu...)
Affinity DataIC50:  1.52E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263763(Biphenyl-4-ylmethyl-imidazol-1-yl-(4-methoxy-benzy...)
Affinity DataIC50:  1.53E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263922(1-[2-Biphenyl-4-yl-1-(4-methoxy-benzyl)-ethyl]-1H-...)
Affinity DataIC50:  1.68E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263666(Biphenyl-4-ylmethyl-(4-tert-butyl-benzyl)-imidazol...)
Affinity DataIC50:  2.16E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263721(Biphenyl-4-ylmethyl-imidazol-1-yl-(4-methyl-benzyl...)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263463(CHEMBL514514 | N-(benzo[b]thiophen-7-ylmethyl)-N-(...)
Affinity DataIC50:  2.49E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263718(Biphenyl-4-ylmethyl-imidazol-1-yl-(2-methyl-benzyl...)
Affinity DataIC50:  2.96E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263764(Biphenyl-4-ylmethyl-(2,4-dichloro-benzyl)-imidazol...)
Affinity DataIC50:  3.65E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263665(CHEMBL478648 | N-(2,4-dichlorobenzyl)-N-(naphthale...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263664(CHEMBL478647 | N-(4-tert-butylbenzyl)-N-(naphthale...)
Affinity DataIC50:  4.59E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263341(CHEMBL478024 | N-(4-tert-butylbenzyl)-N-(4-phenylb...)
Affinity DataIC50:  5.06E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263342(CHEMBL517816 | N-(4-tert-butylbenzyl)-N-(thiophen-...)
Affinity DataIC50:  9.23E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263462(CHEMBL475943 | N-benzyl-N-(benzo[b]thiophen-7-ylme...)
Affinity DataIC50:  9.96E+3nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50264032(CHEMBL491010 | N-(naphthalen-1-ylmethyl)-N-(4-phen...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Università

Curated by ChEMBL
LigandPNGBDBM50263340(CHEMBL478023 | N-(2,4-dichlorobenzyl)-N-(4-phenylb...)
Affinity DataIC50:  1.73E+4nMAssay Description:Inhibition of human aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540671(CHEMBL4635907)
Affinity DataIC50: >3.00E+4nMAssay Description:Displacement of Tracer Red from human ERG measured after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540668(CHEMBL4637717)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP1A2 expressed in baculovirus infected insect cells using luciferin-1A2 as substrate preincubated with enzyme-substr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540669(CHEMBL4637524)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP1A2 expressed in baculovirus infected insect cells using luciferin-1A2 as substrate preincubated with enzyme-substr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540670(CHEMBL4633550)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP1A2 expressed in baculovirus infected insect cells using luciferin-1A2 as substrate preincubated with enzyme-substr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540671(CHEMBL4635907)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP1A2 expressed in baculovirus infected insect cells using luciferin-1A2 as substrate preincubated with enzyme-substr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540668(CHEMBL4637717)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP2D6 expressed in baculovirus infected insect cells using luciferin-ME as substrate preincubated with enzyme/substra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540669(CHEMBL4637524)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP2D6 expressed in baculovirus infected insect cells using luciferin-ME as substrate preincubated with enzyme/substra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540670(CHEMBL4633550)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP2D6 expressed in baculovirus infected insect cells using luciferin-ME as substrate preincubated with enzyme/substra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540671(CHEMBL4635907)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP2D6 expressed in baculovirus infected insect cells using luciferin-ME as substrate preincubated with enzyme/substra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Irbm

Curated by ChEMBL
LigandPNGBDBM50540668(CHEMBL4637717)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human microsomal CYP3A4 expressed in baculovirus infected insect cells using luciferin-IPA as substrate preincubated with enzyme/substr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Displayed 1 to 50 (of 56 total ) | Next | Last >>
Jump to: