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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
38
hits in this display
Target
Histamine receptor H4
(GUINEA PIG)
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
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Affinity Data
Ki: 0.100nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine receptor H4
(GUINEA PIG)
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.150nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.150nM
More data for this Ligand-Target Pair
Target Info
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Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.5nM
More data for this Ligand-Target Pair
Target Info
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Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.5nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H1 receptor
(Cavia porcellus (domestic guinea pig))
Queen'S Medical Centre
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.5nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.550nM
Assay Description:
Displacement of [3H[N-alpha-methylhistamine form human recombinant histamine H3 receptor expressed in CHO cells after 1 hr by liquid scintillation co...
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.700nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.700nM
Assay Description:
Binding affinity to the human histamine H3 receptor
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.800nM
Assay Description:
Displacement of [3H]N-alpha-methylhistamine from human histamine H3 receptor expressed in SK-N-MC cells
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 0.880nM
Assay Description:
Inhibition of Histamine H3 receptor
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H2 receptor
(Cavia porcellus (domestic guinea pig))
Queen'S Medical Centre
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.20nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.25nM
More data for this Ligand-Target Pair
Target Info
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Ligand Info
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Article
PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.5nM
More data for this Ligand-Target Pair
Target Info
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Ligand Info
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Target
Histamine H3 receptor
(GUINEA PIG)
Schering-Plough Research Institute
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.5nM
Assay Description:
Binding affinity of compound towards Histamine H3 receptor was determined in guinea pig brain tissue using [3H]- N alpha-methylhistamine radioligand
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(GUINEA PIG)
Schering-Plough Research Institute
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.5nM
Assay Description:
Binding afinity against Histamine H3 receptor
More data for this Ligand-Target Pair
Target Info
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ChEBI
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Article
PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.90nM
More data for this Ligand-Target Pair
Target Info
KEGG
UniProtKB/TrEMBL
GoogleScholar
Ligand Info
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PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.10nM
More data for this Ligand-Target Pair
Target Info
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Ligand Info
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ChEBI
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In Depth
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PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.70nM
Assay Description:
Antagonist potency against human histamine H3 receptor expressed in CHO cells was determined by GTPgamma-S-assay
More data for this Ligand-Target Pair
Target Info
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ChEBI
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.98nM
More data for this Ligand-Target Pair
Target Info
KEGG
UniProtKB/TrEMBL
GoogleScholar
Ligand Info
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ChEBI
CHEMBL
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PC sid
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
More data for this Ligand-Target Pair
Target Info
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UniProtKB/TrEMBL
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Copy BDB DOI
Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 6nM
Assay Description:
Ligand displacement assays were performed on The SK-N-MC/hH3R cell homogenates. Retained radioactivity was determined by liquid scintillation countin...
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 9.12nM
More data for this Ligand-Target Pair
Target Info
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ChEBI
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Copy BDB DOI
Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 25.1nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H4 receptor
(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 146nM
Assay Description:
Binding affinity to the human histamine H4 receptor
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H4 receptor
(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 146nM
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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ChEBI
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Copy BDB DOI
Target
Histamine H4 receptor
(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 184nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in SK-NM-C cells
More data for this Ligand-Target Pair
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Copy BDB DOI
Target
Histamine H4 receptor
(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 232nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H4 receptor
(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 251nM
Assay Description:
Ligand displacement assays were performed on The SK-N-MC/hH4R cell homogenates. Retained radioactivity was determined by liquid scintillation countin...
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H4 receptor
(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 348nM
More data for this Ligand-Target Pair
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Target
Histamine H3 receptor
(GUINEA PIG)
Schering-Plough Research Institute
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 813nM
More data for this Ligand-Target Pair
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Target
Hrh3 protein
(RAT)
U. 109
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.06E+3nM
More data for this Ligand-Target Pair
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Target
Histamine H3 receptor
(GUINEA PIG)
Schering-Plough Research Institute
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.55E+3nM
More data for this Ligand-Target Pair
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Target
Histamine H1 receptor
(Cavia porcellus (domestic guinea pig))
Queen'S Medical Centre
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding afinity against H1 receptor
More data for this Ligand-Target Pair
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Target
Histamine H1 receptor
(Cavia porcellus (domestic guinea pig))
Queen'S Medical Centre
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Binding affinity of the compound to H-1 receptor was determined in guinea pig brain tissue using [3H]- N alpha-methylhistamine ligand
More data for this Ligand-Target Pair
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Pfizer
Curated by
ChEMBL
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
Copy SMILES
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Affinity Data
IC50: 1.5nM
Assay Description:
Inhibition of rat histamine H3 receptor
More data for this Ligand-Target Pair
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Smithkline Beecham Pharmaceuticals
Curated by
PDSP K
i
Database
Ligand
BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)
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Affinity Data
EC50: 2.80nM
Assay Description:
Agonist activity at human recombinant histamine H3 receptor expressed in CHO cells assessed as [35S]GTPgammaS binding after 1 hr by liquid scintillat...
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Target Info
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Ligand Info
Purchase
ChEBI
CHEMBL
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Article
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