Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50279820 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_29225 |
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IC50 | 4310000±n/a nM |
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Citation | Han, SY; Mayer, SC; Schweiger, EJ; Davis, BM; Joulleé, MM Synthesis and biological activity of galanthamine derivatives as acetylcholinesterase (AChE) inhibitors Bioorg Med Chem Lett1:579-580 (1991) Article |
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More Info.: | Get all data from this article, Assay Method |
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Acetylcholinesterase |
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Name: | Acetylcholinesterase |
Synonyms: | ACES_RAT | Acetylcholinesterase (AChE) | Acetylcholinesterase and butyrylcholinesterase (AChE and BChE) | Acetylcholinesterase precursor | Acetylcholinesterase, AChE | Ache |
Type: | Enzyme |
Mol. Mass.: | 68193.62 |
Organism: | Rattus norvegicus (rat) |
Description: | P37136 |
Residue: | 614 |
Sequence: | MRPPWYPLHTPSLASPLLFLLLSLLGGGARAEGREDPQLLVRVRGGQLRGIRLKAPGGPV
SAFLGIPFAEPPVGSRRFMPPEPKRPWSGILDATTFQNVCYQYVDTLYPGFEGTEMWNPN
RELSEDCLYLNVWTPYPRPTSPTPVLIWIYGGGFYSGASSLDVYDGRFLAQVEGTVLVSM
NYRVGTFGFLALPGSREAPGNVGLLDQRLALQWVQENIAAFGGDPMSVTLFGESAGAASV
GMHILSLPSRSLFHRAVLQSGTPNGPWATVSAGEARRRATLLARLVGCPPGGAGGNDTEL
ISCLRTRPAQDLVDHEWHVLPQESIFRFSFVPVVDGDFLSDTPDALINTGDFQDLQVLVG
VVKDEGSYFLVYGVPGFSKDNESLISRAQFLAGVRIGVPQASDLAAEAVVLHYTDWLHPE
DPAHLRDAMSAVVGDHNVVCPVAQLAGRLAAQGARVYAYIFEHRASTLTWPLWMGVPHGY
EIEFIFGLPLDPSLNYTVEERIFAQRLMQYWTNFARTGDPNDPRDSKSPRWPPYTTAAQQ
YVSLNLKPLEVRRGLRAQTCAFWNRFLPKLLSATDTLDEAERQWKAEFHRWSSYMVHWKN
QFDHYSKQERCSDL
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BDBM50279820 |
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n/a |
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Name | BDBM50279820 |
Synonyms: | 14-(ethylaminocarbonyloxy)-9-methoxy-4-methyl-(1S,12S,14R)-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene | CHEMBL153912 |
Type | Small organic molecule |
Emp. Form. | C20H26N2O4 |
Mol. Mass. | 358.4314 |
SMILES | CCNC(=O)O[C@@H]1C[C@@H]2Oc3c4c(CN(C)CC[C@@]24C=C1)ccc3OC |c:21| |
Structure |
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