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TargetCannabinoid receptor 1(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50556532(CHEMBL4753891)
Affinity DataKi:  0.790nMAssay Description:Displacement of [3H]-CP55,940 from human CB1R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCannabinoid receptor 2(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50601131(CHEMBL5193398)
Affinity DataKi:  1.40nMAssay Description:Displacement of [3H]-CP55,940 from human CB2R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCannabinoid receptor 2(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50601132(CHEMBL5204176)
Affinity DataKi:  1.90nMAssay Description:Displacement of [3H]-CP55,940 from human CB2R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256789(CHEMBL4082361)
Affinity DataKi:  2.10nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256787(CHEMBL4105131)
Affinity DataKi:  2.5nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256758(CHEMBL4059883)
Affinity DataKi:  3.20nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256787(CHEMBL4105131)
Affinity DataKi:  4.90nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256757(CHEMBL4063781)
Affinity DataKi:  5.40nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122942(5-(3,5-Bis-trifluoromethyl-phenyl)-penta-2,4-dieno...)
Affinity DataKi:  5.60nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50072775(2-((1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohe...)
Affinity DataKi:  6.60nMAssay Description:Displacement of [3H]-CP55,940 from human CB1R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
TargetCannabinoid receptor 2(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50556532(CHEMBL4753891)
Affinity DataKi:  7nMAssay Description:Displacement of [3H]-CP55,940 from human CB2R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122938(5-(3,5-Bis-trifluoromethyl-phenyl)-pentanoic acid ...)
Affinity DataKi:  7.80nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256774(CHEMBL4075621)
Affinity DataKi:  8nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256769(CHEMBL4094824)
Affinity DataKi:  8.40nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256788(CHEMBL4068637)
Affinity DataKi:  8.5nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256789(CHEMBL4082361)
Affinity DataKi:  8.70nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256769(CHEMBL4094824)
Affinity DataKi:  8.80nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256757(CHEMBL4063781)
Affinity DataKi:  9.10nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122941(5-[4-(3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluoro-octy...)
Affinity DataKi:  9.20nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122945(5-[4-(3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluoro-oct-...)
Affinity DataKi:  11nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM10880(AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...)
Affinity DataKi:  12nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122940((2S,5S)-(E,E)-8-(5-(4-(trifluoromethyl)phenyl)-2,4...)
Affinity DataKi:  12nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122939(5-(4-Trifluoromethyl-phenyl)-pentanoic acid (5-hyd...)
Affinity DataKi:  13nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50057509((2S,5S)-8-Dec-1-ynyl-5-hydroxymethyl-2-isopropyl-1...)
Affinity DataKi:  15nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122944(5-Phenyl-penta-2,4-dienoic acid (5-hydroxymethyl-2...)
Affinity DataKi:  16nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256770(CHEMBL4067935)
Affinity DataKi:  17nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50570253(CHEMBL4467500)
Affinity DataKi:  19nMAssay Description:Displacement of [3H]-CP55,940 from human CB2R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCarbonic anhydrase 2(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256775(CHEMBL4076976)
Affinity DataKi:  22nMAssay Description:Inhibition of recombinant human carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256788(CHEMBL4068637)
Affinity DataKi:  25nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50072775(2-((1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohe...)
Affinity DataKi:  34nMAssay Description:Displacement of [3H]-CP55,940 from human CB2R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122937(5-Phenyl-pentanoic acid (5-hydroxymethyl-2-isoprop...)
Affinity DataKi:  34nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256774(CHEMBL4075621)
Affinity DataKi:  40nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256758(CHEMBL4059883)
Affinity DataKi:  53nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256770(CHEMBL4067935)
Affinity DataKi:  91nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM50256775(CHEMBL4076976)
Affinity DataKi:  96nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122946(CHEMBL334195 | Hexanoic acid (5-hydroxymethyl-2-is...)
Affinity DataKi:  225nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Human)
Prince Sattam Bin Abdulaziz University

Curated by ChEMBL
LigandPNGBDBM10880(AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...)
Affinity DataKi:  250nMAssay Description:Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins by stopped flow CO2 hydration assayMore data for this Ligand-Target Pair
TargetProtein kinase C alpha type(Human)
Georgetown University Medical Center

Curated by ChEMBL
LigandPNGBDBM50122943(CHEMBL420170 | Hexa-2,4-dienoic acid (5-hydroxymet...)
Affinity DataKi:  1.97E+3nMAssay Description:Displacement of PDBU from recombinant Protein kinase C alpha with phosphatidylserineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50601131(CHEMBL5193398)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-CP55,940 from human CB1R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCannabinoid receptor 1(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50570253(CHEMBL4467500)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-CP55,940 from human CB1R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCannabinoid receptor 1(Human)
University of Pisa

Curated by ChEMBL
LigandPNGBDBM50601132(CHEMBL5204176)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]-CP55,940 from human CB1R expressed in CHO-K1 cell membranes assessed as inhibition constant incubated for 2 hrs by liquid scinti...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM25028(4-[2-(1H-indazol-4-yl)-6-[(4-methanesulfonylpipera...)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of PI3Kalpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistone deacetylase 1(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50606478(CHEMBL5220511)
Affinity DataIC50:  0.580nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCyclin-dependent kinase 4(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50606473(CHEMBL5220945)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of Cdk4 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetEpidermal growth factor receptor(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50029668(AZD-9291 | Osimertinib | US10085983, Compound AZD-...)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of EGFR T790M (unknown origin) incubated for 40 mins in presence of ATPMore data for this Ligand-Target Pair
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50606482(CHEMBL5220907)
Affinity DataIC50:  2nMAssay Description:Inhibition of PDE5 (unknown origin) incubated for 1.5 hrs by IMAP fluorescence polarization phosphodiesterase evaluation assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCyclin-dependent kinase 4(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50110183(Abemaciclib | LY-2835219 | US10626107, Example LY2...)
Affinity DataIC50:  2nMAssay Description:Inhibition of Cdk4 (unknown origin)More data for this Ligand-Target Pair
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50335827((6R,12aR)6-(2,4-Dichlorophenyl)-2-ethyl-2,3,6,7,12...)
Affinity DataIC50:  2nMAssay Description:Inhibition of human recombinant PDE5A-mediated hydrolysis of cGMP after 30 mins by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50335827((6R,12aR)6-(2,4-Dichlorophenyl)-2-ethyl-2,3,6,7,12...)
Affinity DataIC50:  2nMAssay Description:Inhibition of human recombinant PDE5 after 30 mins by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Human)
Menoufia University

Curated by ChEMBL
LigandPNGBDBM50029668(AZD-9291 | Osimertinib | US10085983, Compound AZD-...)
Affinity DataIC50:  2.20nMAssay Description:Inhibition of EGFR wildtype (unknown origin) incubated for 40 mins in presence of ATPMore data for this Ligand-Target Pair
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