| Identification | Back Directory | [Name]
Lysicamine | [CAS]
15444-20-9 | [Synonyms]
Lysicamine
Oxonuciferine
1,2-Dimethoxy-7H-dibenzo[de,g]quinolin-7-one
7H-Dibenzo[de,g]quinolin-7-one, 1,2-dimethoxy- | [Molecular Formula]
C18H13NO3 | [MDL Number]
MFCD01711485 | [MOL File]
15444-20-9.mol | [Molecular Weight]
291.3 |
| Chemical Properties | Back Directory | [Melting point ]
210-1 °c (dec.). | [Boiling point ]
509.4±45.0 °C(Predicted) | [density ]
1.323±0.06 g/cm3(Predicted) | [form ]
Solid | [pka]
2.67±0.20(Predicted) | [color ]
Light yellow to yellow | [InChI]
InChI=1S/C18H13NO3/c1-21-13-9-10-7-8-19-16-14(10)15(18(13)22-2)11-5-3-4-6-12(11)17(16)20/h3-9H,1-2H3 | [InChIKey]
DPBMWJXWUINLQT-UHFFFAOYSA-N | [SMILES]
N1C2=C3C(=C(OC)C(OC)=CC3=CC=1)C1=CC=CC=C1C2=O |
| Hazard Information | Back Directory | [Description]
This oxodibenzoquinoline alkaloid occurs in Lysichiton camtschatcense Schott
var. japonicum Makino. Being a fully conjugated molecule, the alkaloid is
coloured, yielding yellow needles when crystallized from EtOH. The ultraviolet
spectrum in neutral solution (EtOH) has absorption maxima at 235, 270, 307
and 400 mil. In acid solution (EtOH-O.l N/HCl), the absorption maxima occur at
249,276,306 and 453 mil. The structure has been established by synthesis as
1 :2-dimethoxy-7-oxodibenzo[de, gj quinoline. | [Uses]
Lyscamine has shown to have cytotoxicity against various human cancer cells. It can also be enriched using response surface method and adsorption on macroporous resin. | [Definition]
ChEBI: A natural product found in Annona glabra. | [References]
Katsui et al., Tetrahedron Lett., 6257 (1966) |
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