Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50504429 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2215319 (CHEMBL5128451) |
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IC50 | 440±n/a nM |
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Citation | Kumar, N; Kumar, V; Anand, P; Kumar, V; Ranjan Dwivedi, A; Kumar, V Advancements in the development of multi-target directed ligands for the treatment of Alzheimer's disease. Bioorg Med Chem61:0 (2022) [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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BDBM50504429 |
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n/a |
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Name | BDBM50504429 |
Synonyms: | CHEMBL4455506 |
Type | Small organic molecule |
Emp. Form. | C22H27NO4 |
Mol. Mass. | 369.4541 |
SMILES | CCN(CC)Cc1ccc(\C=C\C(=O)c2ccc(OC)c(OC)c2)cc1O |
Structure |
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