Inhibitors | Comment | Organism | Structure |
---|---|---|---|
(5'-amino-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-[4-(3-piperidin-1-yl-propoxy)-phenyl]-methanone | 50% inhibition at 0.0020 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
(5'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-[4-(3-piperidin-1-yl-propoxy)-phenyl]-methanone | 50% inhibition at 0.0015 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
(5-nitro-pyridin-2-yl)-[4-(3-piperidin-1-yl-propoxy)-benzyl]-amine | 50% inhibition at 0.0042 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
(5-nitro-pyridin-2-yl)-{2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-ethyl}-amine | 50% inhibition at 0.0028 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
(5-nitro-pyridin-2-yl)-{3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-propyl}-amine | 50% inhibition at 0.0017 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
(5-nitro-pyridin-2-yl)-{4-[4-(3-piperidin-1-yl-propoxy)-phenyl]-butyl}-amine | 50% inhibition at 0.0017 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
1-(3-(4-(3,4-dihydro-2H-pyrrol-5-yl)phenoxy)propyl)piperidine | 50% inhibition at 0.0090 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
2-(3-piperidin-1-ylpropoxy)-1,3-benzothiazole quinoline | 50% inhibition at 0.021 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
5-nitro-2-(3-piperidin-1-ylpropoxy)pyridine | 50% inhibition at 0.034 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
5-nitro-N-(4-(3-piperidin-1-ylpropoxy)phenyl)pyridin-2-amine | 50% inhibition at 0.0038 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
6-(3-piperidin-1-ylpropoxy)pyridin-3-amine | 50% inhibition at 0.053 mM, simultaneously a potent H3 receptor ligand | Rattus norvegicus | |
6-piperidin-1-yl-1-[4-(3-piperidin-1-yl-propoxy)-phenyl]-hexan-1-one | 50% inhibition at 0.0089 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
7-chloro-4-(3-piperidin-1-ylpropoxy)quinoline | 50% inhibition at 0.0026 mM, simultaneously a potent H3 receptor ligand | Rattus norvegicus | |
N2-[2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-ethyl]-pyridine-2,5-diamine | 50% inhibition at 0.00031 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
N2-[3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-propyl]-pyridine-2,5-diamine | 50% inhibition at 0.0013 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
N2-[4-[4-(3-piperidin-1-yl-propoxy)-phenyl]-butyl]-pyridine-2,5-diamine | 50% inhibition at 0.00034 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus | |
[4-(3-piperidin-1-yl-propoxy)-phenyl]-(1-quinolin-4-yl-piperidin-4-yl)-methanone | 50% inhibition at 0.00031 mM, simultaneously a highly potent H3 receptor ligand | Rattus norvegicus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Rattus norvegicus | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
kidney | - |
Rattus norvegicus | - |
Synonyms | Comment | Organism |
---|---|---|
Ntau-methyltransferase | - |
Rattus norvegicus |