(1S,11R,13R,16R,18S)-11-ethoxy-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁴,⁸]icosa-2,4(8),9,19-tetraene
AlkaPlorer ID: AK010077
Synonym: None
IUPAC Name: (1R,11R,13S,16R,18R)-11-ethoxy-18-methoxy-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene
Structure
SMILES: CCO[C@@H]1O[C@@H]2CN[C@@H]3C[C@@H](OC)C=C[C@@]32C2=CC3=C(C=C21)OCO3
InChI: InChI=1S/C19H23NO5/c1-3-22-18-12-7-14-15(24-10-23-14)8-13(12)19-5-4-11(21-2)6-16(19)20-9-17(19)25-18/h4-5,7-8,11,16-18,20H,3,6,9-10H2,1-2H3/t11-,16+,17+,18+,19+/m0/s1
InChIKey: DWXXGLPEQMCHLG-JZQXSHSJSA-N
Reference
Acetylcholinesterase Enzyme Inhibitory Effects of Amaryllidaceae Alkaloids
PubChem CID: 162917457
LOTUS: LTS0221883
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Crinum bulbispermum | Crinum | Amaryllidaceae | Asparagales | Magnoliopsida | Streptophyta | Viridiplantae | Eukaryota |
Properties Information
Molecule Weight: 345.3950000000001
TPSA？: 58.18000000000001
MolLogP？: 2.0337
Number of H-Donors: 1
Number of H-Acceptors: 6
RingCount: 5
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|