Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50039716 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_28150 (CHEMBL644105) |
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IC50 | 55±n/a nM |
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Citation | Villalobos, A; Blake, JF; Biggers, CK; Butler, TW; Chapin, DS; Chen, YL; Ives, JL; Jones, SB; Liston, DR; Nagel, AA Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase. J Med Chem37:2721-34 (1994) [PubMed] |
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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_HUMAN | ACHE | Acetylcholinesterase (AChE) | Acetylcholinesterase (human AChE) |
Type: | Enzyme |
Mol. Mass.: | 67792.70 |
Organism: | Homo sapiens (Human) |
Description: | P22303 |
Residue: | 614 |
Sequence: | MRPPQCLLHTPSLASPLLLLLLWLLGGGVGAEGREDAELLVTVRGGRLRGIRLKTPGGPV
SAFLGIPFAEPPMGPRRFLPPEPKQPWSGVVDATTFQSVCYQYVDTLYPGFEGTEMWNPN
RELSEDCLYLNVWTPYPRPTSPTPVLVWIYGGGFYSGASSLDVYDGRFLVQAERTVLVSM
NYRVGAFGFLALPGSREAPGNVGLLDQRLALQWVQENVAAFGGDPTSVTLFGESAGAASV
GMHLLSPPSRGLFHRAVLQSGAPNGPWATVGMGEARRRATQLAHLVGCPPGGTGGNDTEL
VACLRTRPAQVLVNHEWHVLPQESVFRFSFVPVVDGDFLSDTPEALINAGDFHGLQVLVG
VVKDEGSYFLVYGAPGFSKDNESLISRAEFLAGVRVGVPQVSDLAAEAVVLHYTDWLHPE
DPARLREALSDVVGDHNVVCPVAQLAGRLAAQGARVYAYVFEHRASTLSWPLWMGVPHGY
EIEFIFGIPLDPSRNYTAEEKIFAQRLMRYWANFARTGDPNEPRDPKAPQWPPYTAGAQQ
YVSLDLRPLEVRRGLRAQACAFWNRFLPKLLSATDTLDEAERQWKAEFHRWSSYMVHWKN
QFDHYSKQDRCSDL
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BDBM50039716 |
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n/a |
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Name | BDBM50039716 |
Synonyms: | 3-(2-(1-benzylpiperidin-4-yl)ethyl)benzo[d]isoxazole | 3-[2-(1-Benzyl-piperidin-4-yl)-ethyl]-benzo[d]isoxazole | CHEMBL92460 |
Type | Small organic molecule |
Emp. Form. | C21H24N2O |
Mol. Mass. | 320.4281 |
SMILES | C(Cc1noc2ccccc12)C1CCN(Cc2ccccc2)CC1 |
Structure |
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