Inhibitors | Comment | Organism | Structure |
---|---|---|---|
1-[ (3-benzoylamino-phenylcarbamoyl)-methyl]-pyridinium chloride | 51% inhibition at 0.05 mM | Homo sapiens | |
1-[(3-benzoylamino-phenylcarbamoyl)-methyl]-3-carbamoyl-pyridiniumchloride | 54% inhibition at 0.05 mM | Homo sapiens | |
1-[(3-benzoylamino-phenylcarbamoyl)-methyl]-3-phenethylcarbamoyl-pyridinium chloride | 55% inhibition at 0.05 mM | Homo sapiens | |
1-[(3-m-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | 61% inhibition at 0.05 mM | Homo sapiens | |
1-[(3-p-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | 42% inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-chloro-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-3-phenethylcarbamoyl-pyridinium chloride | 78% inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-chloro-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | complete inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-methoxy-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-3-phenethylcarbamoyl-pyridinium chloride | 44% inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-methoxy-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | complete inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-methoxy-phenylsulfamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | 50% inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-methyl-benzoylamino)-phenylcarbamoyl]-methyl]-3-phenethylcarbamoyl-pyridinium chloride | complete inhibition at 0.05 mM | Homo sapiens | |
1-[[3-(4-methyl-benzoylamino)-phenylcarbamoyl]-methyl]-pyridinium chloride | - |
Homo sapiens | |
1[[3-(4-methyl-benzoylamino)-phenylcarbamoyl]-methyl]-pyridinium chloride | 68% inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[(3-m-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | 44% inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[(3-p-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | 69% inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[[3-(4-chloro-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | 64% inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[[3-(4-methoxy-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | complete inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[[3-(4-methoxy-phenylsulfamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | 34% inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[[3-(4-methyl-benzoylamino)-phenylcarbamoyl]-methyl]-pyridinium chloride | 24% inhibition at 0.05 mM | Homo sapiens | |
3-carbamoyl-1-[[3-(toluene-4-sulfonylamino)-phenylcarbamoyl]-methyl]-pyridinium chloride | 4% inhibition at 0.05 mM | Homo sapiens | |
3-phenethylcarbamoyl-1-[(3-m-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | 58% inhibition at 0.05 mM | Homo sapiens | |
3-phenethylcarbamoyl-1-[(3-p-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | 72% inhibition at 0.05 mM | Homo sapiens | |
3-phenethylcarbamoyl-1-[[3-(toluene-4-sulfonylamino)-phenylcarbamoyl]-methyl]-pyridinium chloride | 36% inhibition at 0.05 mM | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Synonyms | Comment | Organism |
---|---|---|
BACE-1 | - |
Homo sapiens |
beta-secretase | - |
Homo sapiens |
IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
---|---|---|---|---|---|
0.001 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 1-[[3-(4-chloro-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | |
0.0019 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 3-carbamoyl-1-[[3-(4-methoxy-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | |
0.0022 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 1-[[3-(4-methyl-benzoylamino)-phenylcarbamoyl]-methyl]-3-phenethylcarbamoyl-pyridinium chloride | |
0.0037 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 1-[[3-(4-methoxy-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | |
0.004 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 3-phenethylcarbamoyl-1-[(3-p-tolylcarbamoyl-phenylcarbamoyl)-methyl]-pyridinium chloride | |
0.012 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 1-[[3-(4-chloro-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-3-phenethylcarbamoyl-pyridinium chloride | |
0.013 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 1-[[3-(4-methyl-benzoylamino)-phenylcarbamoyl]-methyl]-pyridinium chloride | |
0.0302 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 3-carbamoyl-1-[[3-(4-chloro-phenylcarbamoyl)-phenylcarbamoyl]-methyl]-pyridinium chloride | |
0.0447 | - |
in 50 mM sodium acetate, pH 4.5, at 37°C | Homo sapiens | 1-[(3-benzoylamino-phenylcarbamoyl)-methyl]-3-carbamoyl-pyridiniumchloride |