Compile Data Set for Download or QSAR
Found 167 with Last Name = 'rodrigues' and Initial = 'cr'
TargetKallikrein-1(Homo sapiens (Human))
Universidade Federal Fluminense

Curated by ChEMBL
LigandPNGBDBM50205620(CHEMBL3943212)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2WW7KNVPubMed
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-...)copy SMILEScopy InChI
Affinity DataIC50: 0.331nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 0.479nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417809(CHEMBL1651249)copy SMILEScopy InChI
Affinity DataIC50: 0.490nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 0.575nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417798(CHEMBL1651247)copy SMILEScopy InChI
Affinity DataIC50: 0.794nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 0.955nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417791(CHEMBL1651139)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417787(CHEMBL1651132)copy SMILEScopy InChI
Affinity DataIC50: 1.29nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417786(CHEMBL1651131)copy SMILEScopy InChI
Affinity DataIC50: 2.51nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50032165(CHEMBL92736 | CHEMBL94217 | N-{3-[2-(1-Benzyl-pipe...)copy SMILEScopy InChI
Affinity DataIC50: 2.82nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417793(CHEMBL1651243)copy SMILEScopy InChI
Affinity DataIC50: 2.88nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.63nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417785(CHEMBL1651129)copy SMILEScopy InChI
Affinity DataIC50: 3.63nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 4.27nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417799(CHEMBL1651248)copy SMILEScopy InChI
Affinity DataIC50: 4.57nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417788(CHEMBL1651134)copy SMILEScopy InChI
Affinity DataIC50: 4.90nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417803(CHEMBL1651133)copy SMILEScopy InChI
Affinity DataIC50: 5.13nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277559(CHEMBL4162056)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 5.75nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277551(A-839977 | CHEMBL1628691)copy SMILEScopy InChI
Affinity DataIC50: 6.60nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50034002(3-(1-Benzyl-piperidin-4-yl)-1-(2-methyl-benzothiaz...)copy SMILEScopy InChI
Affinity DataIC50: 6.76nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039713(3-(2-(1-benzylpiperidin-4-yl)ethyl)-7-methoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 7.08nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039712(3-(2-(1-benzylpiperidin-4-yl)ethyl)-5-methoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 7.24nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039728(3-(2-(1-benzylpiperidin-4-yl)ethyl)-5-methylbenzo[...)copy SMILEScopy InChI
Affinity DataIC50: 7.76nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039717(3-(2-(1-benzylpiperidin-4-yl)ethyl)-6-methoxybenzo...)copy SMILEScopy InChI
Affinity DataIC50: 8.32nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039723(3-(2-(1-benzylpiperidin-4-yl)ethyl)benzo[d]isoxazo...)copy SMILEScopy InChI
Affinity DataIC50: 8.71nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417792(CHEMBL1651140)copy SMILEScopy InChI
Affinity DataIC50: 8.71nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039727(CHEMBL93123 | N-(3-(2-(1-benzylpiperidin-4-yl)ethy...)copy SMILEScopy InChI
Affinity DataIC50: 9.33nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417802(CHEMBL1651130)copy SMILEScopy InChI
Affinity DataIC50: 9.77nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50034003(3-(1-Benzyl-piperidin-4-yl)-1-(2-methyl-1H-benzoim...)copy SMILEScopy InChI
Affinity DataIC50: 12.0nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417808(CHEMBL1651246)copy SMILEScopy InChI
Affinity DataIC50: 14.1nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417794(CHEMBL1651244)copy SMILEScopy InChI
Affinity DataIC50: 15.8nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039719(3-(2-(1-benzylpiperidin-4-yl)ethyl)benzo[d]isoxazo...)copy SMILEScopy InChI
Affinity DataIC50: 19.9nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Rattus norvegicus (Rat))
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277551(A-839977 | CHEMBL1628691)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Tested for inhibitory potency against rat liver microsomal squalene synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277551(A-839977 | CHEMBL1628691)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced platelet aggregation in human whole bloodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetP2X purinoceptor 7(Mus musculus)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277551(A-839977 | CHEMBL1628691)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced platelet aggregation in human whole bloodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50464474(CHEMBL4281588)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Antagonist activity at human P2X7R expressed in HEK293 cells assessed as inhibition of ATP-induced ethidium iodide uptake preincubated for 10 mins fo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6V7KPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417783(CHEMBL1651126)copy SMILEScopy InChI
Affinity DataIC50: 22.9nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Mus musculus)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50464474(CHEMBL4281588)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Antagonist activity at P2X7R in Swiss Webster mouse peritoneal macrophages assessed as inhibition of ATP-induced propidium iodide uptake preincubated...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6V7KPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417801(CHEMBL1651127)copy SMILEScopy InChI
Affinity DataIC50: 25.1nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50039731(3-(2-(1-benzylpiperidin-4-yl)ethyl)benzo[d]isoxazo...)copy SMILEScopy InChI
Affinity DataIC50: 25.7nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50034000(3-(1-Benzyl-piperidin-4-yl)-1-(2,3-dihydro-benzo[1...)copy SMILEScopy InChI
Affinity DataIC50: 30.2nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417796(CHEMBL1651125)copy SMILEScopy InChI
Affinity DataIC50: 33.1nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Homo sapiens (Human))
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277551(A-839977 | CHEMBL1628691)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:In vitro thromboxane A2 receptor antagonism through inhibition of U-46619 induced contraction of rat isolated thoracic aortic stripMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417784(CHEMBL1651128)copy SMILEScopy InChI
Affinity DataIC50: 39.8nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Mus musculus)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50277559(CHEMBL4162056)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of BzATP-induced current at holding potential of -6...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50417800(CHEMBL1651250)copy SMILEScopy InChI
Affinity DataIC50: 42.7nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetP2X purinoceptor 7(Mus musculus)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50234965(A-740003 | CHEMBL255787 | N-(1-(2-cyano-3-(quinoli...)copy SMILEScopy InChI
Affinity DataIC50: 47nMAssay Description:Antagonist activity at P2X7 receptor in Swiss mouse peritoneal macrophages assessed as inhibition of BzATP-induced current at holding potential of -6...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3HWCPubMed
TargetP2X purinoceptor 7(Mus musculus)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50464477(CHEMBL4292211)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Antagonist activity at P2X7R in Swiss Webster mouse peritoneal macrophages assessed as inhibition of ATP-induced propidium iodide uptake preincubated...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6V7KPubMed
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