Compile Data Set for Download or QSAR
Found 49 with Last Name = 'molinski' and Initial = 'tf'
TargetCathepsin E(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50382733(CHEMBL2024289)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of cathepsin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23F4QNRPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599319(Aplysamine-2 | CHEMBL2062972)copy SMILES
Affinity DataIC50: 460nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599316(APLYSINAMISINE II | Aplysinamisine II)copy SMILES
Affinity DataIC50: 770nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599319(Aplysamine-2 | CHEMBL2062972)copy SMILES
Affinity DataIC50: 1.03E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599322(CHEMBL5206414)copy SMILES
Affinity DataIC50: 1.18E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599320(PURPUREAMINE I | Purpuramine-1 | Purpureamine I)copy SMILES
Affinity DataIC50: 2.71E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599314(CHEMBL5182821)copy SMILES
Affinity DataIC50: 3.32E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetLaccase(Trametes versicolor)
University of California

Curated by ChEMBL
LigandPNGBDBM50357700(PTILOMYCALIN A)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of Trametes versicolor laccase assessed as production of dopachrome using 100 uM epinephrine as substrate preincubated for 30 mins before ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SJ1M1JPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599318(CHEMBL5191097)copy SMILES
Affinity DataIC50: 4.79E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetLaccase(Trametes versicolor)
University of California

Curated by ChEMBL
LigandPNGBDBM50357700(PTILOMYCALIN A)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of Trametes versicolor laccase assessed as production of dopachrome using 200 uM dopamine as substrate preincubated for 30 mins before sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SJ1M1JPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599320(PURPUREAMINE I | Purpuramine-1 | Purpureamine I)copy SMILES
Affinity DataIC50: 5.40E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599315(CHEMBL5180215)copy SMILES
Affinity DataIC50: 5.74E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetLaccase(Trametes versicolor)
University of California

Curated by ChEMBL
LigandPNGBDBM50357700(PTILOMYCALIN A)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibition of Trametes versicolor laccase assessed as production of dopachrome using 300 uM L-dopa as substrate preincubated for 30 mins before subst...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SJ1M1JPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599317(CHEMBL5184002)copy SMILES
Affinity DataIC50: 5.80E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599318(CHEMBL5191097)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599316(APLYSINAMISINE II | Aplysinamisine II)copy SMILES
Affinity DataIC50: 1.03E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599317(CHEMBL5184002)copy SMILES
Affinity DataIC50: 1.07E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599313(CHEMBL5200837)copy SMILES
Affinity DataIC50: 1.40E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599314(CHEMBL5182821)copy SMILES
Affinity DataIC50: 1.54E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599322(CHEMBL5206414)copy SMILES
Affinity DataIC50: 1.96E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599321(CHEMBL5183798)copy SMILES
Affinity DataIC50: 1.99E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50599313(CHEMBL5200837)copy SMILES
Affinity DataIC50: 1.00E+5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599321(CHEMBL5183798)copy SMILES
Affinity DataIC50: 1.00E+5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50599315(CHEMBL5180215)copy SMILES
Affinity DataIC50: 1.00E+5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1R0RPubMed
TargetLaccase(Trametes versicolor)
University of California

Curated by ChEMBL
LigandPNGBDBM26985(2-triaza-1,2-diyne | CHEMBL79455 | CHEMBL89295 | N...)copy SMILEScopy InChI
Affinity DataIC50: 2.57E+5nMAssay Description:Inhibition of Trametes versicolor laccase assessed as production of dopachrome using 200 uM dopamine as substrate preincubated for 30 mins before sub...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SJ1M1JPubMed
TargetLaccase(Trametes versicolor)
University of California

Curated by ChEMBL
LigandPNGBDBM26985(2-triaza-1,2-diyne | CHEMBL79455 | CHEMBL89295 | N...)copy SMILEScopy InChI
Affinity DataIC50: 2.63E+5nMAssay Description:Inhibition of Trametes versicolor laccase assessed as production of dopachrome using 100 uM epinephrine as substrate preincubated for 30 mins before ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SJ1M1JPubMed
TargetLaccase(Trametes versicolor)
University of California

Curated by ChEMBL
LigandPNGBDBM26985(2-triaza-1,2-diyne | CHEMBL79455 | CHEMBL89295 | N...)copy SMILEScopy InChI
Affinity DataIC50: 2.79E+5nMAssay Description:Inhibition of Trametes versicolor laccase assessed as production of dopachrome using 300 uM L-dopa as substrate preincubated for 30 mins before subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SJ1M1JPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475846(CHEMBL376941)copy SMILEScopy InChI
Affinity DataEC50:  2.40E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475845(CHEMBL209427)copy SMILEScopy InChI
Affinity DataEC50:  2.00E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475844(CHEMBL210076)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475843(CHEMBL377741)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475842(CHEMBL377812)copy SMILEScopy InChI
Affinity DataEC50:  6.50E+3nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50191286(Bastadin-5 | CHEMBL439151 | bastadin 5)copy SMILEScopy InChI
Affinity DataEC50:  2.20E+3nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475841(CHEMBL377464)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475840(CHEMBL380242)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475839(CHEMBL386432)copy SMILEScopy InChI
Affinity DataEC50:  2.09E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50191278((+/-)-5,17-dibromo-4-hydroxy-2-oxa-10-aza-tricyclo...)copy SMILEScopy InChI
Affinity DataEC50:  1.09E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475838(CHEMBL378025)copy SMILEScopy InChI
Affinity DataEC50:  2.86E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475837(CHEMBL212154)copy SMILEScopy InChI
Affinity DataEC50:  2.10E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetPeptidyl-prolyl cis-trans isomerase FKBP1A/Ryanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50475836(CHEMBL213687)copy SMILEScopy InChI
Affinity DataEC50:  3.30E+4nMAssay Description:Agonist like activity at skeletal junction sarcoplasmic reticulum RyR1/FKBP12 complex assessed as increase in [3H]ryanodine bindingMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23R0WNDPubMed
TargetRyanodine receptor 1(Oryctolagus cuniculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50241985((E,Z)bastadin-19 | Bastadin-19 | CHEMBL506286 | CH...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Displacement of [3H]ryanodine from Ry1R/FKBP12 receptor complex in rabbit sarcoplasmic reticulumMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D59PubMed
TargetRyanodine receptor 1(Oryctolagus cuniculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50292368(CHEMBL498932 | bastadin 20)copy SMILEScopy InChI
Affinity DataEC50:  2.06E+4nMAssay Description:Displacement of [3H]ryanodine from Ry1R/FKBP12 receptor complex in rabbit sarcoplasmic reticulumMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D59PubMed
TargetRyanodine receptor 1(Oryctolagus cuniculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50292367(15,34-O-disulfatobastadin 7 | CHEMBL509326)copy SMILEScopy InChI
Affinity DataEC50:  1.36E+4nMAssay Description:Displacement of [3H]ryanodine from Ry1R/FKBP12 receptor complex in rabbit sarcoplasmic reticulumMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D59PubMed
TargetRyanodine receptor 1(Oryctolagus cuniculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50292366(10-sulfatobastadin 3 | CHEMBL450681)copy SMILEScopy InChI
Affinity DataEC50:  1.00E+5nMAssay Description:Displacement of [3H]ryanodine from Ry1R/FKBP12 receptor complex in rabbit sarcoplasmic reticulumMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D59PubMed
TargetRyanodine receptor 1(Oryctolagus cuniculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50191286(Bastadin-5 | CHEMBL439151 | bastadin 5)copy SMILEScopy InChI
Affinity DataEC50:  2.00E+3nMAssay Description:Displacement of [3H]ryanodine from Ry1R/FKBP12 receptor complex in rabbit sarcoplasmic reticulumMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D59PubMed
TargetRyanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50241985((E,Z)bastadin-19 | Bastadin-19 | CHEMBL506286 | CH...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+5nMAssay Description:Displacement of [3H]ryanodine from RyR1 calcium channel in sarcoplasmic reticulum assessed as calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM587TPubMed
TargetRyanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50241986(Bastadin-10 | CHEMBL504851)copy SMILEScopy InChI
Affinity DataEC50:  5.80E+3nMAssay Description:Displacement of [3H]ryanodine from RyR1 calcium channel in sarcoplasmic reticulum assessed as calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM587TPubMed
TargetRyanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50241983(Bastadin 4 | Bastadin-4 | CHEMBL453147)copy SMILEScopy InChI
Affinity DataEC50:  1.47E+4nMAssay Description:Displacement of [3H]ryanodine from RyR1 calcium channel in sarcoplasmic reticulum assessed as calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM587TPubMed
TargetRyanodine receptor 1(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM50241984(BASTADIN 6 | CHEMBL505907 | bastadin-6)copy SMILEScopy InChI
Affinity DataEC50:  2.60E+3nMAssay Description:Displacement of [3H]ryanodine from RyR1 calcium channel in sarcoplasmic reticulum assessed as calcium mobilizationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM587TPubMed