Compile Data Set for Download or QSAR
Found 176 with Last Name = 'o''donnell' and Initial = 'mm'
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50026926(8-{4-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-butyl}-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142638(8-[4-(4-Pyrimidin-2-yl-piperazin-1-yl)-pentyl]-8-a...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177756(CHEMBL202472 | N-(2,6-diethylphenyl)-4-hydroxy-3-m...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177740(CHEMBL371637 | N-(2-ethyl-6-methylphenyl)-4-hydrox...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142640(8-{3-Hydroxy-4-[4-(2-methoxy-phenyl)-piperazin-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177763(CHEMBL201834 | N-(2,6-dimethylphenyl)-4-hydroxy-3-...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50026924(8-[4-(4-Phenyl-piperazin-1-yl)-butyl]-8-aza-spiro[...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177752(CHEMBL202607 | N-(2,6-dichlorophenyl)-4-hydroxy-3-...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177764(CHEMBL383691 | N-(2-chloro-6-methylphenyl)-4-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50001859((buspirone) 8-[4-(4-Pyrimidin-2-yl-piperazin-1-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177748(CHEMBL202500 | N-(2-chloro-6-methylphenyl)-4-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177746(CHEMBL202624 | N-(2-bromophenyl)-4-hydroxy-N-propy...)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177749(CHEMBL202155 | N-(2-bromophenyl)-4-hydroxy-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177757(CHEMBL264655 | N-(2-chlorophenyl)-4-hydroxy-N-prop...)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142643(8-{4-[4-(5-Fluoro-pyrimidin-2-yl)-piperazin-1-yl]-...)copy SMILEScopy InChI
Affinity DataIC50: 46nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177744(CHEMBL204185 | N-(2-chlorophenyl)-4-hydroxy-3-meth...)copy SMILEScopy InChI
Affinity DataIC50: 51nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177736(4-hydroxy-N-propyl-N-(2-(trifluoromethyl)phenyl)be...)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50019422(2-[4-(4-Pyrimidin-2-yl-piperazin-1-yl)-butyl]-isoi...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177760(CHEMBL372997 | N-(2-bromophenyl)-4-hydroxy-N-propy...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142649(8-{4-[4-(5-Fluoro-pyrimidin-2-yl)-piperazin-1-yl]-...)copy SMILEScopy InChI
Affinity DataIC50: 63nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142647(8-{4-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-butyl}-8...)copy SMILEScopy InChI
Affinity DataIC50: 64nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142639(8-{4-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-3-hydrox...)copy SMILEScopy InChI
Affinity DataIC50: 69nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177755(CHEMBL203565 | N-(2-fluorophenyl)-4-hydroxy-N-prop...)copy SMILEScopy InChI
Affinity DataIC50: 74nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372257(CHEMBL271914)copy SMILEScopy InChI
Affinity DataIC50: 78nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142648(1-{4-[4-(5-Fluoro-pyrimidin-2-yl)-piperazin-1-yl]-...)copy SMILEScopy InChI
Affinity DataIC50: 87nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177762(CHEMBL202248 | N-(2-bromophenyl)-N-ethyl-4-hydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142642(8-{4-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-pentyl}-...)copy SMILEScopy InChI
Affinity DataIC50: 99nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177753(4-hydroxy-3-methyl-N-propyl-N-o-tolylbenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 109nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50005132(4,4-Dimethyl-1-[4-(4-pyrimidin-2-yl-piperazin-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM16755(Acylguanidine, 10d | N-[(1Z)-amino[(3-hydroxypropy...)copy SMILEScopy InChI
Affinity DataIC50: 121nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372264(CHEMBL430034)copy SMILEScopy InChI
Affinity DataIC50: 124nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372267(CHEMBL428075)copy SMILEScopy InChI
Affinity DataIC50: 125nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372266(CHEMBL273186)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372263(CHEMBL256000)copy SMILEScopy InChI
Affinity DataIC50: 137nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetCathepsin D(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372242(CHEMBL404166)copy SMILEScopy InChI
Affinity DataIC50: 144nMAssay Description:Inhibition of cathepsin DMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372256(CHEMBL272970)copy SMILEScopy InChI
Affinity DataIC50: 172nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372255(CHEMBL271422)copy SMILEScopy InChI
Affinity DataIC50: 203nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372258(CHEMBL269943)copy SMILEScopy InChI
Affinity DataIC50: 203nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142650(1-{4-[4-(5-Fluoro-pyrimidin-2-yl)-piperazin-1-yl]-...)copy SMILEScopy InChI
Affinity DataIC50: 205nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
ArQule Inc

Curated by ChEMBL
LigandPNGBDBM50142636(2-{4-[4-(5-Fluoro-pyrimidin-2-yl)-piperazin-1-yl]-...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:In vitro binding affinity of the compound against 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT in human CYP3A4 assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1KB5PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177735(CHEMBL426849 | N-allyl-4-hydroxy-N-phenylbenzenesu...)copy SMILEScopy InChI
Affinity DataIC50: 235nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM16754(2-[2-(adamantan-1-yl)-5-phenyl-1H-pyrrol-1-yl]-N-[...)copy SMILEScopy InChI
Affinity DataIC50: 239nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372254(CHEMBL272719)copy SMILEScopy InChI
Affinity DataIC50: 241nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177737(CHEMBL204434 | N-biphenyl-2-yl-4-hydroxy-3-methyl-...)copy SMILEScopy InChI
Affinity DataIC50: 253nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372250(CHEMBL404897)copy SMILEScopy InChI
Affinity DataIC50: 255nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372238(CHEMBL438355)copy SMILEScopy InChI
Affinity DataIC50: 255nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372261(CHEMBL272718)copy SMILEScopy InChI
Affinity DataIC50: 269nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50177743(CHEMBL203402 | N-ethyl-4-hydroxy-N-(4-hydroxypheny...)copy SMILEScopy InChI
Affinity DataIC50: 272nMAssay Description:Inhibition of binding to ER in Ad5-wt-ER-infected HAECT1 cells by NFkappaB-mediated luciferase reporterMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CC107BPubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372242(CHEMBL404166)copy SMILEScopy InChI
Affinity DataIC50: 276nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50372265(CHEMBL270820)copy SMILEScopy InChI
Affinity DataIC50: 278nMAssay Description:Inhibition of BACE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PK8PubMed
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