Inhibitors | Comment | Organism | Structure |
---|---|---|---|
(3aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo(2,3-b)indol-5-yl (2-methylphenyl)carbamate | 50% inhibition at 10 nM | Homo sapiens | |
(3aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo(2,3-b)indol-5-yl (4-isopropylphenyl)carbamate | 50% inhibition at 760 nM | Homo sapiens | |
(3aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo(2,3-b)indol-5-yl ethylcarbamate | 50% inhibition at 94 nM | Homo sapiens | |
(3aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo(2,3-b)indol-5-yl methylcarbamate | 50% inhibition at 28 nM | Homo sapiens | |
(3aR)-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo(2,3-b)indol-5-yl (2-methylphenyl)carbamate | 50% inhibition at 13 nM | Homo sapiens | |
(3aR)-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo(2,3-b)indol-5-yl (4-isopropylphenyl)carbamate | 50% inhibition at 3860 nM | Homo sapiens | |
(3aR)-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo(2,3-b)indol-5-yl ethylcarbamate | 50% inhibition at 82 nM | Homo sapiens | |
(3aR)-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo(2,3-b)indol-5-yl methylcarbamate | 50% inhibition at 27 nM | Homo sapiens | |
1-methyl-8,10-dioxatricyclo(7.2.1.0 2,7)dodeca-2,4,6-trien-5-yl (2-methylphenyl)carbamate | 50% inhibition at 56 nM | Homo sapiens | |
1-methyl-8,10-dioxatricyclo(7.2.1.0 2,7)dodeca-2,4,6-trien-5-yl (4-isopropylphenyl)carbamate | 50% inhibition at 4300 nM | Homo sapiens | |
1-methyl-8,10-dioxatricyclo(7.2.1.0 2,7)dodeca-2,4,6-trien-5-yl ethylcarbamate | 50% inhibition at 830 nM | Homo sapiens | |
2'-ethylphenylgeneserine N-oxide | 50% inhibition at 125 nM | Homo sapiens | |
3a-methyl-2,3,3a,8a-tetrahydrofuro(2,3-b)(1)benzofuran-5-yl (2-methylphenyl)carbamate | 50% inhibition at 23 nM | Homo sapiens | |
3a-methyl-2,3,3a,8a-tetrahydrofuro(2,3-b)(1)benzofuran-5-yl (4-isopropylphenyl)carbamate | 50% inhibition at 2650 nM | Homo sapiens | |
3a-methyl-2,3,3a,8a-tetrahydrofuro(2,3-b)(1)benzofuran-5-yl ethylcarbamate | 50% inhibition at 360 nM | Homo sapiens | |
donepezil | 50% inhibition at 22 nM | Homo sapiens | |
eptastigmine | 50% inhibition at 22 nM | Homo sapiens | |
galanthamine | 50% inhibition at 800 nM | Homo sapiens | |
huperzine A | 50% inhibition above 47 nM | Homo sapiens | |
additional information | comparison of 50% inhibitory concentration for EC 3.1.1.7 and EC 3.1.1.8 | Homo sapiens | |
phenserine | 50% inhibition at 22 nM | Homo sapiens | |
rivastigmine | 50% inhibition at 4150 nM | Homo sapiens | |
tacrine | 50% inhibition at 190 nM | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
erythrocyte | - |
Homo sapiens | - |