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Found 438 with Last Name = 'rodrigues' and Initial = 'c'
TargetSqualene synthase(Trypanosoma cruzi)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50052351(3-Biphenyl-4-yl-1-aza-bicyclo[2.2.2]octan-3-ol | 3...)
Affinity DataKi:  62nMAssay Description:Inhibition of Trypanosoma cruzi squalene synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSqualene synthase(Trypanosoma cruzi)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50052351(3-Biphenyl-4-yl-1-aza-bicyclo[2.2.2]octan-3-ol | 3...)
Affinity DataKi:  62nMAssay Description:Inhibition of Trypanosoma cruzi squalene synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495338(CHEMBL3110147)
Affinity DataKi:  133nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495344(CHEMBL3110154)
Affinity DataKi:  257nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495345(CHEMBL3110149)
Affinity DataKi:  297nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495339(CHEMBL3110146)
Affinity DataKi:  516nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495349(CHEMBL3110153)
Affinity DataKi:  598nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495343(CHEMBL3110145)
Affinity DataKi:  612nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495342(CHEMBL3110151)
Affinity DataKi:  641nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495349(CHEMBL3110153)
Affinity DataKi:  733nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495343(CHEMBL3110145)
Affinity DataKi:  802nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495341(CHEMBL3110150)
Affinity DataKi:  808nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495342(CHEMBL3110151)
Affinity DataKi:  815nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495347(CHEMBL3110152)
Affinity DataKi:  847nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetKallikrein-1(Homo sapiens (Human))
Universidade Federal Fluminense

Curated by ChEMBL
LigandPNGBDBM50205620(CHEMBL3943212)
Affinity DataKi:  3.10E+3nMAssay Description:Competitive inhibition of recombinant human KLK1 expressed in baculovirus/insect cell expression system using Abz-KLRSSKQ-EDDnp peptide as substrate ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495346(CHEMBL3110148)
Affinity DataKi:  3.24E+3nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495340(CHEMBL3110155)
Affinity DataKi:  3.81E+3nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495339(CHEMBL3110146)
Affinity DataKi:  2.79E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495347(CHEMBL3110152)
Affinity DataKi:  2.80E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495341(CHEMBL3110150)
Affinity DataKi:  4.70E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495338(CHEMBL3110147)
Affinity DataKi:  4.73E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495344(CHEMBL3110154)
Affinity DataKi:  4.76E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495340(CHEMBL3110155)
Affinity DataKi:  6.40E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495345(CHEMBL3110149)
Affinity DataKi:  7.22E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495346(CHEMBL3110148)
Affinity DataKi:  9.45E+4nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495348(CHEMBL3110156)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495337(CHEMBL3110157)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495337(CHEMBL3110157)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-2-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Instituto Militar De Engenharia

Curated by ChEMBL
LigandPNGBDBM50495348(CHEMBL3110156)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of human recombinant carbonic anhydrase-1-mediated CO2 hydration by stopped-flow assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50032162(3-[2-(1-Benzyl-piperidin-4-yl)-ethyl]-5,7-dihydro-...)
Affinity DataIC50:  0.331nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50032161(3-[2-(1-Benzyl-piperidin-4-yl)-ethyl]-7-methyl-5,7...)
Affinity DataIC50:  0.479nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417809(CHEMBL1651249)
Affinity DataIC50:  0.490nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50032164(3-(2-(1-benzylpiperidin-4-yl)ethyl)-5,6-dihydroiso...)
Affinity DataIC50:  0.575nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417798(CHEMBL1651247)
Affinity DataIC50:  0.794nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50032163(3-(2-(1-benzylpiperidin-4-yl)ethyl)-5H-isoxazolo[5...)
Affinity DataIC50:  0.955nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417791(CHEMBL1651139)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417787(CHEMBL1651132)
Affinity DataIC50:  1.29nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417786(CHEMBL1651131)
Affinity DataIC50:  2.51nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50032165(CHEMBL92736 | CHEMBL94217 | N-{3-[2-(1-Benzyl-pipe...)
Affinity DataIC50:  2.82nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417793(CHEMBL1651243)
Affinity DataIC50:  2.88nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50032160(3-(2-(1-benzylpiperidin-4-yl)ethyl)-6H-isoxazolo[5...)
Affinity DataIC50:  3.63nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417785(CHEMBL1651129)
Affinity DataIC50:  3.63nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50034001(3-(1-Benzyl-piperidin-4-yl)-1-(1-ethyl-2-methyl-1H...)
Affinity DataIC50:  4.27nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417799(CHEMBL1651248)
Affinity DataIC50:  4.57nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417788(CHEMBL1651134)
Affinity DataIC50:  4.90nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50417803(CHEMBL1651133)
Affinity DataIC50:  5.13nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto De Tecnologia Em F£Rmacos

Curated by ChEMBL
LigandPNGBDBM50277559(CHEMBL4162056)
Affinity DataIC50:  5.30nMAssay Description:Antagonist activity at human P2X7 receptor expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 10...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal Do Rio De Janeiro (Ufrj)

Curated by ChEMBL
LigandPNGBDBM50039729(3-(2-(1-benzylpiperidin-4-yl)ethyl)-5,6-dimethylbe...)
Affinity DataIC50:  5.75nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetE3 ubiquitin-protein ligase Mdm2(Homo sapiens (Human))
Universidade De Lisboa

Curated by ChEMBL
LigandPNGBDBM50590814(CHEMBL5182359)
Affinity DataIC50:  6nMAssay Description:Inhibition of MDM2 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto De Tecnologia Em F£Rmacos

Curated by ChEMBL
LigandPNGBDBM50277551(A-839977 | CHEMBL1628691)
Affinity DataIC50:  6.60nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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