Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50289093 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_28155 |
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IC50 | >100000±n/a nM |
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Citation | Jaen, JC; Gregor, VE; Lee, C; Davis, R; Emmerling, M Acetylcholinesterase inhibition by fused dihydroquinazoline compounds Bioorg Med Chem Lett6:737-742 (1996) 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_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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BDBM50289093 |
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n/a |
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Name | BDBM50289093 |
Synonyms: | 3-Chloro-12-oxo-6,7,8,9,10,12-hexahydro-azepino[2,1-b]quinazolin-5-ium | 3-Chloro-7,8,9,10-tetrahydro-6H-azepino[2,1-b]quinazolin-12-one | CHEMBL165292 |
Type | Small organic molecule |
Emp. Form. | C13H13ClN2O |
Mol. Mass. | 248.708 |
SMILES | Clc1ccc2c(c1)nc1CCCCCn1c2=O |
Structure |
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