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Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
82
hits in this display
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.339nM
Assay Description:
Displacement of [3H]-LSD from 5HT7 receptor (unknown origin) transfected in HEK293 cells incubated for 1.5 hrs by liquid scintillation counting
More data for this Ligand-Target Pair
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Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.339nM
Assay Description:
Displacement of [3H]LSD from human 5-HT7 receptor expressed in HEK cell membranes after 1.5 hrs by microbeta scintillation counting method
More data for this Ligand-Target Pair
Target Info
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Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.339nM
Assay Description:
Displacement of [3H]LSD from 5-HT7 receptor (unknown origin) expressed in CHO-K1 cells by liquid scintillation counting method
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.340nM
Assay Description:
Displacement of [3H]-LSD from 5HT7 receptor (unknown origin) transfected in HEK293 cells incubated for 1.5 hrs by liquid scintillation counting
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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GoogleScholar
Ligand Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.340nM
Assay Description:
Displacement of [3H]LSD from human 5-HT7 receptor expressed in HEK cell membranes after 1.5 hrs by microbeta scintillation counting method
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.340nM
Assay Description:
Displacement of [3H]D-lysergic acid diethylamide from 5HT7R (unknown origin) expressed in HEK293 cell membranes incubated for 1.5 hrs in absence of l...
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.340nM
Assay Description:
Displacement of [3H]LSD from 5-HT7 receptor (unknown origin) expressed in CHO-K1 cells by liquid scintillation counting method
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.340nM
Assay Description:
Displacement of [3H]LSD from 5-HT7R (unknown origin) expressed in CHO-K1 cells by liquid scintillation counting method
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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antibodypedia
GoogleScholar
Ligand Info
Purchase
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.710nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from human 5-HT7 receptor expressed in CHOK1 cells after 30 mins by liquid scintillation counting analysis
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.710nM
Assay Description:
Displacement of [3H]-5-HT from recombinant human 5-HT7A receptor expressed in CHOK1 cell membranes after 40 mins by liquid scintillation counting met...
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.710nM
Assay Description:
Displacement of [3H]-5-HT from human 5-HT7 receptor expressed in CHOK1 cell membranes after 30 mins by liquid scintillation spectrometry
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.710nM
Assay Description:
Displacement of [3H]-5-HT from human 5-HT7 receptor expressed in CHOK1 cell membranes after 30 mins by liquid scintillation spectrometry
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
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GoogleScholar
Ligand Info
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CHEMBL
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 5A
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.780nM
Assay Description:
Binding affinity to 5HT5A receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
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Target
5-hydroxytryptamine receptor 7
(Rattus norvegicus (rat))
State University Of Groningen
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1nM
Assay Description:
Binding affinity towards rat 5-HT7 receptor expressed in HEK cells
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1nM
Assay Description:
Binding affinity to 5HT7 receptor
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
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PC sid
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In Depth
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1nM
Assay Description:
Binding affinity towards human 5-hydroxytryptamine 7 receptor on HEK293 cells using radioligand [3H]-LSD
More data for this Ligand-Target Pair
Target Info
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KEGG
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CHEMBL
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In Depth
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.20nM
Assay Description:
Displacement of [3H]-5-CT from human 5-HT7 receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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GoogleScholar
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CHEMBL
MCE
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.20nM
Assay Description:
Binding affinity to human cloned 5HT7 receptor expressed in HEK293 cells
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
UniProtKB/SwissProt
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GoogleScholar
Ligand Info
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CHEMBL
MCE
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PC sid
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In Depth
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.20nM
Assay Description:
Displacement of [3H]-5-CT from human 5-HT7b receptor expressed in HEK293 cells after 1 hr
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Rattus norvegicus (rat))
State University Of Groningen
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.26nM
Assay Description:
Displacement of [3H]-5-HT from rat 5-hydroxytryptamine 7 receptor expressed in CHO cells
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.26nM
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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CHEMBL
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PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Displacement of [3H]5-HT from human 5HT7 receptor transfected in CFO-K1 cells after 30 mins by liquid scintillation spectrometry
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
UniProtKB/SwissProt
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CHEMBL
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Binding affinity to 5HT7 receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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GoogleScholar
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CHEMBL
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PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Binding affinity towards cloned human 5-hydroxytryptamine 7 receptor was determined in HEK293 cells using [3H]5-CT as radioligand
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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CHEMBL
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Antagonist activity at 5-HT7 receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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CHEMBL
MCE
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In Depth
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Displacement of [3H]-5-CT from human 5-HT7a receptor expressed in HEK293 cells
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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CHEMBL
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Binding affinity towards human 5-hydroxytryptamine 7 receptor
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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CHEMBL
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PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Displacement of [3H]-5-CT from human 5-HT7a receptor expressed in HEK293 cells
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
UniProtKB/SwissProt
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CHEMBL
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In Depth
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PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Binding affinity for human cloned 5-hydroxytryptamine 7 receptor in HEK 293 using [3H]5-CT as a radioligand
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.30nM
Assay Description:
Binding affinity to human 5-HT7 receptor by radioligand binding assay
More data for this Ligand-Target Pair
Target Info
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CHEMBL
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PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.90nM
Assay Description:
Displacement of [3H]-5-HT from human 5HT7 receptor expressed in CHO-K1 cells incubated for 40 mins in presence of serotonin by liquid scintillation c...
More data for this Ligand-Target Pair
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: <5nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in HEK293 cells
More data for this Ligand-Target Pair
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5-hydroxytryptamine receptor 2B
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 5nM
Assay Description:
Displacement of [3H]-5-HT from human 5-HT2B receptor expressed in HEK293 cells
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5-hydroxytryptamine receptor 2A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: <5nM
Assay Description:
Displacement of [3H]-ketanserin from human 5-HT2A receptor expressed in HEK293 cells
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5-hydroxytryptamine receptor 2C
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: <5nM
Assay Description:
Displacement of [3H]-mesulergine from human 5-HT2C receptor expressed in HEK293 cells
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5-hydroxytryptamine receptor 7
(Rattus norvegicus (rat))
State University Of Groningen
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 32nM
Assay Description:
Binding affinity towards 5-hydroxytryptamine receptor 7 on rat hypothalamus membranes using [3H]5-CT as radioligand.
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5-hydroxytryptamine receptor 5A
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 63.1nM
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Target
5-hydroxytryptamine receptor 5A
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 65nM
Assay Description:
Binding affinity towards 5-hydroxytryptamine 5 receptor
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Target
D(2) dopamine receptor
(Homo sapiens (Human))
Uppsala University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 316nM
Assay Description:
Displacement of [3H]-Raclopride from human dopamine receptor D2A expressed in mouse Ltk cells
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Target
D(2) dopamine receptor
(Homo sapiens (Human))
Uppsala University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 316nM
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5-hydroxytryptamine receptor 1B
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 1.00E+3nM
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5-hydroxytryptamine receptor 4
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
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Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 1.26E+3nM
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5-hydroxytryptamine receptor 1D
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
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Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 1.58E+3nM
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D(3) dopamine receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 2.51E+3nM
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5-hydroxytryptamine receptor 1F
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 3.16E+3nM
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5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >5.00E+3nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in HEK293 cells after 1 hr
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5-hydroxytryptamine receptor 6
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 6.31E+3nM
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Target
5-hydroxytryptamine receptor 1E
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: 6.31E+3nM
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5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 9.02E+3nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in CHOK1 cell membranes after 30 mins by liquid scintillation spectrometry
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 9.02E+3nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from recombinant human 5-HT1A receptor expressed in CHOK1 cell membranes after 1 hr by liquid scintillation counting m...
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 9.02E+3nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from human 5-HT1A receptor expressed in CHOK1 cell membranes after 30 mins by liquid scintillation spectrometry
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: 9.02E+3nM
Assay Description:
Displacement of [3H]-5-HT from human 5-HT1A receptor expressed in CHOK1 cells after 30 mins by liquid scintillation counting analysis
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Target
5-hydroxytryptamine receptor 2A
(Rattus norvegicus (rat))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT2A receptor in rat cortex
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Target
5-hydroxytryptamine receptor 1A
(Rattus norvegicus (rat))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT1A receptor in rat hippocampus
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Displacement of [3H]8-OH-DPAT from human 5-HT1A receptor transfected in CFO-K1 cells after 30 mins by liquid scintillation spectrometry
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Displacement of [3H]-8-OH-DPAT from human 5-hydroxytryptamine 1A receptor expressed in CHO cells
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Target
Alpha-1B adrenergic receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 2C
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 2B
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 2A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 6
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT6 receptor (unknown origin)
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Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 4
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT4 receptor (unknown origin)
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Target
5-hydroxytryptamine receptor 3A
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT3 receptor (unknown origin)
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5-hydroxytryptamine receptor 2C
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT2C receptor (unknown origin)
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Target
5-hydroxytryptamine receptor 2B
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT2B receptor (unknown origin)
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Target
5-hydroxytryptamine receptor 2A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
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Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT2A receptor (unknown origin)
More data for this Ligand-Target Pair
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Target
5-hydroxytryptamine receptor 1E
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT1E receptor (unknown origin)
More data for this Ligand-Target Pair
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Target
5-hydroxytryptamine receptor 1D
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT1D receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
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In Depth
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Copy BDB DOI
Target
5-hydroxytryptamine receptor 1B
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT1B receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
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In Depth
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity to 5HT1A receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
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CHEMBL
MCE
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PC sid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 1A
(Homo sapiens (Human))
Florida A&M University
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Antagonist activity at 5-HT1A receptor (unknown origin)
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
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CHEMBL
MCE
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PC sid
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In Depth
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Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 0.900nM
Assay Description:
Antagonist activity at human 5-HT7 receptor expressed in HEK293 cells assessed as inhibition of Gs protein-mediated cAMP accumulation by luminescence...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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GoogleScholar
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CHEMBL
MCE
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PC sid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 0.930nM
Assay Description:
Antagonist activity at human 5-HT7 receptor expressed in HEK293 cells assessed as reduction in cAMP accumulation incubated for 30 mins by microplate ...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
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CHEMBL
MCE
PC cid
PC sid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 0.930nM
Assay Description:
Antagonist activity at human 5-HT7 receptor expressed in CHO-K1 cells assessed as decrease in serotonin-induced cAMP level after 1 hr by TR-FRET assa...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
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DrugBank
antibodypedia
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Ligand Info
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CHEMBL
MCE
PC cid
PC sid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 0.930nM
Assay Description:
Antagonist activity at human 5-HT7 receptor expressed in HEK293 cells assessed as reduction in cAMP accumulation incubated for 30 mins by microplate ...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 0.933nM
Assay Description:
Antagonist activity at human 5-HT7 receptor expressed in HEK293 cells assessed as inhibition of Gs protein-mediated cAMP accumulation by luminescence...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 2.60nM
Assay Description:
Antagonist activity at human recombinant 5-HT7 receptor expressed in CHOK1 cells measured after 60 mins in the presence of serotonin by LANCE TR-FRET...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 2.60nM
Assay Description:
Antagonist activity at human recombinant 5-HT7 receptor expressed in CHOK1 cells measured after 60 mins in the presence of serotonin by LANCE TR-FRET...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 3.70nM
Assay Description:
Antagonist activity at human 5-HT7R expressed in HEK293 cells assessed as inhibition of serotonin stimulated-cAMP levels preincubated for 10 mins fol...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
PC cid
PC sid
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 3.70nM
Assay Description:
Antagonist activity at human 5-HT7R expressed in HEK293 cells assessed as inhibition of serotonin stimulated-cAMP levels preincubated for 10 mins fol...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
Purchase
CHEMBL
MCE
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
5-hydroxytryptamine receptor 7
(Homo sapiens (Human))
Korea Institute Of Science And Technology
Curated by
ChEMBL
Ligand
BDBM50098551
((R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolid...)
Copy SMILES
Copy InChI
Affinity Data
Kd: 9.70nM
Assay Description:
Binding affinity to 5HT7 receptor
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
UniProtKB/SwissProt
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antibodypedia
GoogleScholar
Ligand Info
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CHEMBL
MCE
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In Depth
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Article
PubMed
Copy BDB DOI
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