(+)-Nornantenine

AlkaPlorer ID: AK036502

Synonym: 'Nornantenine', 'N-Nornantenine'

IUPAC Name: (12S)-18,19-dimethoxy-5,7-dioxa-13-azapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(20),2,4(8),9,16,18-hexaene

Structure

SMILES: COC1=CC2=C3C(=C1OC)C1=CC4=C(C=C1C[C@@H]3NCC2)OCO4

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InChI: InChI=1S/C19H19NO4/c1-21-16-6-10-3-4-20-13-5-11-7-14-15(24-9-23-14)8-12(11)18(17(10)13)19(16)22-2/h6-8,13,20H,3-5,9H2,1-2H3/t13-/m0/s1

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InChIKey: JWXKBCGJLCEZTJ-ZDUSSCGKSA-N

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Reference

Alkaloids of<i>Siparuna tonduziana</i>

PubChem CID: 14395308

LOTUS: LTS0096488

SuperNatural Ⅲ: SN0177507-02

NPASS: NPC298008

data_source: manually

Source

Species Genus Family Order Class Phylum Kingdom Domain

Properties Information

Molecule Weight: 325.36400000000015

TPSA: 48.95

MolLogP: 2.8424000000000005

Number of H-Donors: 1

Number of H-Acceptors: 5

RingCount: 5

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Electrophorus electricus Acetylcholinesterase IC50 205550.0 nM 10.1016/j.bmc.2016.07.043
Electrophorus electricus Acetylcholinesterase Inhibition 50.38 % 10.1016/j.bmc.2016.07.043
Equus caballus Cholinesterase IC50 94450.0 nM 10.1016/j.bmc.2016.07.043
Equus caballus Cholinesterase Inhibition 75.81 % 10.1016/j.bmc.2016.07.043
None Unchecked Ratio IC50 0.46 None 10.1016/j.bmc.2016.07.043
None Unchecked Ratio IC50 2.18 None 10.1016/j.bmc.2016.07.043

Metabolism Information