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Found 1218 Enz. Inhib. hit(s) with Target = 'Calmodulin'
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50304913((2R,3R,4R,5R)-2-(6-amino-2-oxopyrimidin-1(2H)-yl)-...)
Affinity DataKi:  100nMAssay Description:Inhibition of Bacillus anthracis edema factor catalytic domain by radiometric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452691(CHEMBL4218073)
Affinity DataKi:  300nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452676(CHEMBL4206295)
Affinity DataKi:  700nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50206817((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-...)
Affinity DataKi:  980nMAssay Description:Inhibition of Bacillus anthracis edema factor catalytic domain by radiometric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452677(CHEMBL4218072)
Affinity DataKi:  2.10E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452684(CHEMBL4217380)
Affinity DataKi:  3.70E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452675(CHEMBL4211713)
Affinity DataKi:  4.60E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50304912((((((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydr...)
Affinity DataKi:  8.98E+3nMAssay Description:Inhibition of Bacillus anthracis edema factor catalytic domain by radiometric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452681(CHEMBL4209693)
Affinity DataKi:  9.40E+3nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452678(CHEMBL4211326)
Affinity DataKi:  1.09E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-1(Human)
Universidad Nacional AutóNoma De MéXico

Curated by ChEMBL
LigandPNGBDBM50266275(CHEMBL456494 | Tajixanthone hydrate)
Affinity DataKi:  1.39E+4nMAssay Description:Inhibition of recombinant calmodulin (unknown origin) mediated bovine brain PDE1 activation assessed as effect on inorganic phosphate release using v...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452682(CHEMBL4210973)
Affinity DataKi:  1.47E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452683(CHEMBL4215512)
Affinity DataKi:  1.65E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50292495(((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihyd...)
Affinity DataKi:  1.84E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-1(Human)
Universidad Nacional AutóNoma De MéXico

Curated by ChEMBL
LigandPNGBDBM50001888((chloropromazine) [3-(2-Chloro-phenothiazin-10-yl)...)
Affinity DataKi:  1.93E+4nMAssay Description:Inhibition of recombinant calmodulin (unknown origin) mediated bovine brain PDE1 activation assessed as effect on inorganic phosphate release using v...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-1(Human)
Universidad Nacional AutóNoma De MéXico

Curated by ChEMBL
LigandPNGBDBM50266274(14-methoxytajixanthone | CHEMBL515370)
Affinity DataKi:  2.54E+4nMAssay Description:Inhibition of recombinant calmodulin (unknown origin) mediated bovine brain PDE1 activation assessed as effect on inorganic phosphate release using v...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452693(CHEMBL4202426)
Affinity DataKi:  2.59E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452692(CHEMBL4204554)
Affinity DataKi:  2.76E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452694(CHEMBL4203961)
Affinity DataKi:  3.48E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452679(CHEMBL4217046)
Affinity DataKi:  3.77E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452686(CHEMBL4217363)
Affinity DataKi:  3.89E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452697(CHEMBL4204818)
Affinity DataKi:  4.22E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452689(CHEMBL4217944)
Affinity DataKi:  4.96E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452687(CHEMBL4209678)
Affinity DataKi:  5.91E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452688(CHEMBL4208943)
Affinity DataKi:  8.81E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452680(CHEMBL4214117)
Affinity DataKi:  9.65E+4nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452685(CHEMBL4214316)
Affinity DataKi:  1.27E+5nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452695(CHEMBL4207125)
Affinity DataKi:  2.22E+5nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452690(CHEMBL4205857)
Affinity DataKi:  2.86E+5nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-sensitive adenylate cyclase(Bacillus anthracis)
Ernst-Moritz-Arndt-University

Curated by ChEMBL
LigandPNGBDBM50452696(CHEMBL4204524)
Affinity DataKi:  9.55E+5nMAssay Description:Inactivation of Bacillus anthracis edema factor in presence of CaM incubated for 10 to 240 mins by EnzChek pyrophosphate assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-domain protein kinase 1, putative(Cryptosporidium parvum (strain Iowa II))
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389702(CHEMBL2070069 | US10544104, Compound 39 | US112479...)
Affinity DataIC50:  0.400nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1, putative(Cryptosporidium parvum (strain Iowa II))
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389700(CHEMBL2070067 | US10544104, Compound 38 | US112479...)
Affinity DataIC50:  0.600nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389687(CHEMBL2070054 | US10544104, Compound 41 | US112479...)
Affinity DataIC50:  0.600nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389687(CHEMBL2070054 | US10544104, Compound 41 | US112479...)
Affinity DataIC50:  0.600nMAssay Description:Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416615(4-((4-amino-3-(2-cyclopropoxyquinolin-6-yl)-1H-pyr...)
Affinity DataIC50:  0.700nMAssay Description:Inhibitors were evaluated in triplicate in eight-point dilutions (3-fold dilutions) during the enzymatic reactions. TgCDPK1 enzymatic inhibition was ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416611(4-((4-amino-3-(6-cyclopropoxynaphthalen-2-yl)-1H-p...)
Affinity DataIC50:  0.700nMAssay Description:Inhibitors were evaluated in triplicate in eight-point dilutions (3-fold dilutions) during the enzymatic reactions. TgCDPK1 enzymatic inhibition was ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389702(CHEMBL2070069 | US10544104, Compound 39 | US112479...)
Affinity DataIC50:  0.700nMAssay Description:Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389700(CHEMBL2070067 | US10544104, Compound 38 | US112479...)
Affinity DataIC50:  0.700nMAssay Description:Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389702(CHEMBL2070069 | US10544104, Compound 39 | US112479...)
Affinity DataIC50:  0.700nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389700(CHEMBL2070067 | US10544104, Compound 38 | US112479...)
Affinity DataIC50:  0.700nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416551(US10307425, Example 17 | US10632122, Example 17)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of recombinant Toxoplasma gondii CDPK1 using Biotin-C6-PLARTLSVAGLPGKK as substrate after 90 mins in presence of ATP by luciferase reporte...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-domain protein kinase 1, putative(Cryptosporidium parvum (strain Iowa II))
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389698(CHEMBL2070065 | US10544104, Compound 37 | US112479...)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389695(CHEMBL2070062 | US10544104, Compound 40 | US112479...)
Affinity DataIC50:  0.800nMAssay Description:Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416551(US10307425, Example 17 | US10632122, Example 17)
Affinity DataIC50:  0.800nMAssay Description:Inhibitors were evaluated in triplicate in eight-point dilutions (3-fold dilutions) during the enzymatic reactions. TgCDPK1 enzymatic inhibition was ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389695(CHEMBL2070062 | US10544104, Compound 40 | US112479...)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389694(CHEMBL2070060 | US10544104, Compound 42 | US112479...)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM50389694(CHEMBL2070060 | US10544104, Compound 42 | US112479...)
Affinity DataIC50:  0.900nMAssay Description:Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416560(US10307425, Example 26 | US10632122, Example 26)
Affinity DataIC50:  0.900nMAssay Description:Inhibitors were evaluated in triplicate in eight-point dilutions (3-fold dilutions) during the enzymatic reactions. TgCDPK1 enzymatic inhibition was ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416560(US10307425, Example 26 | US10632122, Example 26)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of recombinant Toxoplasma gondii CDPK1 using Biotin-C6-PLARTLSVAGLPGKK as substrate after 90 mins in presence of ATP by luciferase reporte...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University Of Washington Through Its Center For

US Patent
LigandPNGBDBM416558(US10307425, Example 24 | US10632122, Example 24)
Affinity DataIC50:  1nMAssay Description:Inhibitors were evaluated in triplicate in eight-point dilutions (3-fold dilutions) during the enzymatic reactions. TgCDPK1 enzymatic inhibition was ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
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