Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50308338 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_613891 (CHEMBL1067712) |
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IC50 | 12700±n/a nM |
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Citation | Geissler, T; Brandt, W; Porzel, A; Schlenzig, D; Kehlen, A; Wessjohann, L; Arnold, N Acetylcholinesterase inhibitors from the toadstool Cortinarius infractus. Bioorg Med Chem18:2173-7 (2010) [PubMed] 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_BOVIN | ACHE | Acetylcholinesterase (AChE) | Acetylcholinesterase precursor |
Type: | Enzyme |
Mol. Mass.: | 67659.62 |
Organism: | Bos taurus (bovine) |
Description: | n/a |
Residue: | 613 |
Sequence: | MRPPWCPLHTPSLTPPLLLLLFLIGGGAEAEGPEDPELLVMVRGGRLRGLRLMAPRGPVS
AFLGIPFAEPPVGPRRFLPPEPKRPWPGVLNATAFQSVCYQYVDTLYPGFEGTEMWNPNR
ELSEDCLYLNVWTPYPRPSSPTPVLVWIYGGGFYSGASSLDVYDGRFLTQAEGTVLVSMN
YRVGAFGFLALPGSREAPGNVGLLDQRLALQWVQENVAAFGGDPTSVTLFGESAGAASVG
MHLLSPPSRGLFHRAVLQSGAPNGPWATVGVGEARRRATLLARLVGCPPGGAGGNDTELV
ACLRARPAQDLVDHEWRVLPQESVFRFSFVPVVDGDFLSDTPEALINAGDFHGLQVLVGV
VKDEGSYFLVYGAPGFSKDNESLISRAQFLAGVRVGVPQASDLAAEAVVLHYTDWLHPED
PARLREALSDVVGDHNVVCPVAQLAGRLAAQGARVYAYIFEHRASTLSWPLWMGVPHGYE
IEFIFGLPLEPSLNYTIEERTFAQRLMRYWANFARTGDPNDPRDPKAPQWPPYTAGAQQY
VSLNLRPLEVRRGLRAQACAFWNRFLPKLLSATDTLDEAERQWKAEFHRWSSYMVHWKNQ
FDHYSKQDRCSDL
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BDBM50308338 |
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n/a |
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Name | BDBM50308338 |
Synonyms: | 10-Hydroxy-infractopicrin | CHEMBL589071 |
Type | Small organic molecule |
Emp. Form. | C17H13N2O2 |
Mol. Mass. | 277.2968 |
SMILES | Oc1ccc2c(c1)c1cc[n+]3CCCc4cc(=O)n2c1c34 |
Structure |
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