Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50139052 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1549993 (CHEMBL3755444) |
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Ki | 17000±n/a nM |
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Citation | Lemes, LF; de Andrade Ramos, G; de Oliveira, AS; da Silva, FM; de Castro Couto, G; da Silva Boni, M; Guimarães, MJ; Souza, IN; Bartolini, M; Andrisano, V; do Nascimento Nogueira, PC; Silveira, ER; Brand, GD; Soukup, O; Korábecný, J; Romeiro, NC; Castro, NG; Bolognesi, ML; Romeiro, LA Cardanol-derived AChE inhibitors: Towards the development of dual binding derivatives for Alzheimer's disease. Eur J Med Chem108:687-700 (2016) [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_ELEEL | Acetylcholinesterase (AChE) | Acetylcholinesterase (EeAChE) | ache |
Type: | Enzyme |
Mol. Mass.: | 71812.79 |
Organism: | Electrophorus electricus (Electric eel) |
Description: | n/a |
Residue: | 633 |
Sequence: | MKILDALLFPVIFIMFFIHLSIAQTDPELTIMTRLGQVQGTRLPVPDRSHVIAFLGIPFA
EPPLGKMRFKPPEPKKPWNDVFDARDYPSACYQYVDTSYPGFSGTEMWNPNRMMSEDCLY
LNVWVPATPRPHNLTVMVWIYGGGFYSGSSSLDVYDGRYLAHSEKVVVVSMNYRVSAFGF
LALNGSAEAPGNVGLLDQRLALQWVQDNIHFFGGNPKQVTIFGESAGAASVGMHLLSPDS
RPKFTRAILQSGVPNGPWRTVSFDEARRRAIKLGRLVGCPDGNDTDLIDCLRSKQPQDLI
DQEWLVLPFSGLFRFSFVPVIDGVVFPDTPEAMLNSGNFKDTQILLGVNQNEGSYFLIYG
APGFSKDNESLITREDFLQGVKMSVPHANEIGLEAVILQYTDWMDEDNPIKNREAMDDIV
GDHNVVCPLQHFAKMYAQYSILQGQTGTASQGNLGWGNSGSASNSGNSQVSVYLYMFDHR
ASNLVWPEWMGVIHGYEIEFVFGLPLEKRLNYTLEEEKLSRRMMKYWANFARTGNPNINV
DGSIDSRRRWPVFTSTEQKHVGLNTDSLKVHKGLKSQFCALWNRFLPRLLNVTENIDDAE
RQWKAEFHRWSSYMMHWKNQFDHYSKQERCTNL
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BDBM50139052 |
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n/a |
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Name | BDBM50139052 |
Synonyms: | CHEMBL3754700 |
Type | Small organic molecule |
Emp. Form. | C23H33NO2 |
Mol. Mass. | 355.5136 |
SMILES | COc1cccc(CCCCCCCCNCc2ccccc2OC)c1 |
Structure |
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