Compile Data Set for Download or QSAR
Found 180 with Last Name = 'tolomeo' and Initial = 'm'
TargetRibonucleoside-diphosphate reductase large subunit/subunit M2 B(Homo sapiens (Human))
University of Camerino

Curated by ChEMBL
LigandPNGBDBM50497567(CHEMBL3337770)copy SMILEScopy InChI
Affinity DataKi:  4.00E+5nMAssay Description:Competitive inhibition of human recombinant ribonucleotide reductase in presence of varying levels of ATP by Dixon plotMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z18H9PubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50084717((+)-(1R,2R,3S,5S)-methyl 3-(benzoyloxy)-8-methyl-8...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Displacement of [3H]paroxetine from Serotonin transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Universita di Ferrara

Curated by ChEMBL
LigandPNGBDBM12578(2-(imidazol-1-yl)-1-hydroxyethylidene-1,1-bisphosp...)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007730(CHEMBL3233755)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibition of human HDAC-6 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Universita di Ferrara

Curated by ChEMBL
LigandPNGBDBM50273714(CHEMBL446734 | [2-(Imidazol-1-yl)ethyl]-bisphospho...)copy SMILEScopy InChI
Affinity DataIC50: 9.03nMAssay Description:Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76CD8PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166145((3S,6R)-3-[Bis-(4-fluoro-phenyl)-methoxy]-6-methox...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166146((3S,6S)-3-[Bis-(4-fluoro-phenyl)-methoxy]-8-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Universita di Ferrara

Curated by ChEMBL
LigandPNGBDBM50273716(CHEMBL457423 | [2-(Benzoimidazol-1-yl)ethyl]-bisph...)copy SMILEScopy InChI
Affinity DataIC50: 16.1nMAssay Description:Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76CD8PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166135((3S,6S)-3-[Bis-(4-fluoro-phenyl)-methoxy]-6-methox...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Universita di Ferrara

Curated by ChEMBL
LigandPNGBDBM50273717(CHEMBL504429 | [2-(Imidazol-2-yl-thio)ethyl]-bisph...)copy SMILEScopy InChI
Affinity DataIC50: 28.1nMAssay Description:Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76CD8PubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibition of human HDAC-6 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMedDrugBank
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007729(CHEMBL3233488)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166141((3S,6S)-3-[(4-Chloro-phenyl)-phenyl-methoxy]-6-met...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007730(CHEMBL3233755)copy SMILEScopy InChI
Affinity DataIC50: 33nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007731(CHEMBL3233754)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007732(CHEMBL3233752)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM20926(5-[2,4-dihydroxy-5-(propan-2-yl)phenyl]-N-ethyl-4-...)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007733(CHEMBL3233753)copy SMILEScopy InChI
Affinity DataIC50: 68nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007734(CHEMBL3233485)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007735(CHEMBL3233486)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50366775(BENZTROPINE | Benzatropine)copy SMILEScopy InChI
Affinity DataIC50: 118nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166147((3S,6R)-3-[Bis-(4-fluoro-phenyl)-methoxy]-8-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50084717((+)-(1R,2R,3S,5S)-methyl 3-(benzoyloxy)-8-methyl-8...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007736(CHEMBL3233483)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 243nMAssay Description:Inhibition of human HDAC-8 using RHK(Ac)K(Ac) as substrateMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 258nMAssay Description:Inhibition of human HDAC-1 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166151((3S,6S)-3-Benzhydryloxy-6-methoxy-8-methyl-8-aza-b...)copy SMILEScopy InChI
Affinity DataIC50: 276nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166145((3S,6R)-3-[Bis-(4-fluoro-phenyl)-methoxy]-6-methox...)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Displacement of [3H]paroxetine from Serotonin transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166150((3S,6S)-3-[Bis-(4-fluoro-phenyl)-methoxy]-6-methox...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 344nMAssay Description:Inhibition of human HDAC-7 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
TargetHistone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of human HDAC-3/NCOR-2 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 362nMAssay Description:Inhibition of human HDAC-11 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 378nMAssay Description:Inhibition of human HDAC-5 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Universita di Ferrara

Curated by ChEMBL
LigandPNGBDBM50273718(CHEMBL457424 | [2-(Purin-9-yl)ethyl]-bisphosphonic...)copy SMILEScopy InChI
Affinity DataIC50: 388nMAssay Description:Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76CD8PubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166143((3S,6S)-3-[(4-Chloro-phenyl)-phenyl-methoxy]-6-met...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 456nMAssay Description:Inhibition of human HDAC-10 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 493nMAssay Description:Inhibition of human HDAC-4 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007730(CHEMBL3233755)copy SMILEScopy InChI
Affinity DataIC50: 521nMAssay Description:Inhibition of human HDAC-11 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166144((3S,6S)-3-[(4-Chloro-phenyl)-phenyl-methoxy]-8-met...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of human recombinant HDAC1 using modified Boc-Lys(Ac)-AMC MAL as substrate after 1 hr by fluorescent activity assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50026643(CHEMBL3335369)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human recombinant HDAC1 using modified Boc-Lys(Ac)-AMC MAL as substrate after 1 hr by fluorescent activity assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125V70PubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Universita di Ferrara

Curated by ChEMBL
LigandPNGBDBM50273799(CHEMBL452354 | [2-(6-Chloro-purin-9-yl)ethyl]-bisp...)copy SMILEScopy InChI
Affinity DataIC50: 883nMAssay Description:Inhibition of human FPP synthase expressed in Escherichia coli BL21 (DE3)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76CD8PubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007730(CHEMBL3233755)copy SMILEScopy InChI
Affinity DataIC50: 886nMAssay Description:Inhibition of human HDAC-10 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166136((R)-6-[Bis-(4-fluoro-phenyl)-methoxy]-8-methyl-8-a...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50026641(CHEMBL3335367)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human recombinant HDAC1 using modified Boc-Lys(Ac)-AMC MAL as substrate after 1 hr by fluorescent activity assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125V70PubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 921nMAssay Description:Inhibition of human HDAC-2 using RHKK(Ac) as substrateMore data for this Ligand-Target Pair
TargetSimilar to alpha-tubulin isoform 1(Bos taurus)
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50135180(CHEMBL3746143)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of bovine brain tubulin polymerization by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN97GZPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166140((S)-6-[Bis-(4-fluoro-phenyl)-methoxy]-8-methyl-8-a...)copy SMILEScopy InChI
Affinity DataIC50: 1.13E+3nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
Universit£ degli Studi di Ferrara

Curated by ChEMBL
LigandPNGBDBM50007737(CHEMBL3233487)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Displacement of GM-FTC from Hsp90-alpha (unknown origin) after 4 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40WQXPubMed
TargetSodium-dependent dopamine transporter(Rattus norvegicus (rat))
Universit£ di Ferrara

Curated by ChEMBL
LigandPNGBDBM50166139((3S,6S)-3-Benzhydryloxy-8-methyl-8-aza-bicyclo[3.2...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Displacement of [3H]WIN-35428 from Dopamine transporter of rat caudate putamenMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3M8MPubMed
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