Forticine

AlkaPlorer ID: AK013883

Synonym: '', 'Persicanidine A', 'Persicanidine B', 'Ebeiedine', 'Tortifoline', 'Harepermine', 'Petilidine', '(-)-Tortifoline', 'Eduardinine', 'Hupehenine', 'Edpetilidine', 'Songbeinine', 'Ebeinine', 'Delavine'

IUPAC Name: (1R,2S,6S,9R,10S,11R,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol

Structure

SMILES: C[C@H]1CC[C@@H]2[C@@H](C)[C@@H]3CC[C@@H]4[C@@H](C[C@H]5[C@H]4C[C@@H](O)[C@H]4C[C@@H](O)CC[C@@]45C)[C@@H]3CN2C1

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InChI: InChI=1S/C27H45NO2/c1-15-4-7-25-16(2)18-5-6-19-20(22(18)14-28(25)13-15)11-23-21(19)12-26(30)24-10-17(29)8-9-27(23,24)3/h15-26,29-30H,4-14H2,1-3H3/t15-,16-,17-,18-,19+,20+,21-,22+,23-,24+,25+,26+,27+/m0/s1

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InChIKey: NEMWYOKGHGSVSC-SECATLSXSA-N

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Properties Information

Molecule Weight: 415.66200000000026

TPSA: 43.7

MolLogP: 4.563200000000005

Number of H-Donors: 2

Number of H-Acceptors: 3

RingCount: 6

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Electrophorus electricus Acetylcholinesterase IC50 5850.0 nM 10.1016/j.ejmech.2017.06.007
Electrophorus electricus Acetylcholinesterase Inhibition nan % 10.1016/j.ejmech.2017.06.007
Equus caballus Cholinesterase IC50 2080.0 nM 10.1016/j.ejmech.2017.06.007
None Unchecked Ratio IC50 0.36 None 10.1016/j.ejmech.2017.06.007

Metabolism Information