Inhibitors | Comment | Organism | Structure |
---|---|---|---|
4-(1-[4-[acetyl(methyl)amino]-3-methylphenyl]-1-ethylpropyl)-2-methylphenyl diethylcarbamate | 22% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]-3-methylphenyl]-1-ethylpropyl)phenyl diethylcarbamate | 25% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)-2-methylphenyl diethylcarbamate | 56% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl 4-methylpiperazine-1-carboxylate | 17% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl azepane-1-carboxylate | 70% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl azocane-1-carboxylate | 20% inhibition at 0.001 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl bis(1-methylethyl)carbamate | 72% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl bis(1-methylpropyl)carbamate | 22% inhibition at 0.001 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl dibenzylcarbamate | 51% inhibition at 0.001 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl dibutylcarbamate | 32% inhibition at 0.001 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl diethylcarbamate | 57% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl dimethylcarbamate | 29% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl dipropylcarbamate | 77% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl morpholine-4-carboxylate | 15% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl piperidine-1-carboxylate | 68% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-ethylpropyl)phenyl pyrrolidine-1-carboxylate | 57% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-methylethyl)phenyl diethylcarbamate | 16% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]-1-propylbutyl)phenyl diethylcarbamate | 27% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]cyclobutyl)phenyl diethylcarbamate | 16% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]cycloheptyl)phenyl diethylcarbamate | 25% inhibition at 0.01 mM; 46% inhibition at 0.01 mM | Homo sapiens | |
4-(1-[4-[acetyl(methyl)amino]phenyl]cyclopentyl)phenyl diethylcarbamate | 5% inhibition at 0.01 mM | Homo sapiens | |
4-(3-(4-(N-methylacetamido)phenyl)pentan-3-yl)phenyl dibenzylcarbamate | competitive inhibitor | Homo sapiens | |
4-[1-[4-(acetylamino)-3-methylphenyl]-1-ethylpropyl]-2-methylphenyl diethylcarbamate | 17% inhibition at 0.01 mM | Homo sapiens | |
dutasteride | - |
Homo sapiens | |
finasteride | - |
Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
testosterone + NADPH + H+ | - |
Homo sapiens | 5alpha-dihydrotestosterone + NADP+ + H+ | - |
? |
Synonyms | Comment | Organism |
---|---|---|
5alpha-reductase 1 | - |
Homo sapiens |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
NADPH | - |
Homo sapiens |
IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
---|---|---|---|---|---|
0.00084 | - |
- |
Homo sapiens | 4-(3-(4-(N-methylacetamido)phenyl)pentan-3-yl)phenyl dibenzylcarbamate |