Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM170150 |
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Substrate/Competitor | n/a |
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Meas. Tech. | AChE and BChE Inhibition Assay |
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pH | 8±n/a |
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Temperature | 298.15±n/a K |
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IC50 | 4.9e+4± 4e+1 nM |
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Comments | extracted |
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Citation | Mohammadi-Khanaposhtani, M; Mahdavi, M; Saeedi, M; Sabourian, R; Safavi, M; Khanavi, M; Foroumadi, A; Shafiee, A; Akbarzadeh, T Design, Synthesis, Biological Evaluation, and Docking Study of Acetylcholinesterase Inhibitors: New Acridone-1,2,4-oxadiazole-1,2,3-triazole Hybrids. Chem Biol Drug Des86:1425-32 (2015) [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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BDBM170150 |
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n/a |
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Name | BDBM170150 |
Synonyms: | 10-((1-((3-(p-Tolyl)-1,2,4-oxadiazol-5-yl)methyl)-1H-1,2,3-triazol-4-yl)methyl)acridin-9(10H)-one (10a) |
Type | Small organic molecule |
Emp. Form. | C26H20N6O2 |
Mol. Mass. | 448.476 |
SMILES | Cc1ccc(cc1)-c1noc(Cn2cc(Cn3c4ccccc4c(=O)c4ccccc34)nn2)n1 |
Structure |
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