Lysicamine
- CAS NO.:15444-20-9
- Empirical Formula: C18H13NO3
- Molecular Weight: 291.3
- MDL number: MFCD01711485
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-08-28 18:13:45
What is Lysicamine?
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.
The Uses of Lysicamine
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)
Properties of Lysicamine
Melting point: | 210-1 °c (dec.). |
Boiling point: | 509.4±45.0 °C(Predicted) |
Density | 1.323±0.06 g/cm3(Predicted) |
pka | 2.67±0.20(Predicted) |
Safety information for Lysicamine
Computed Descriptors for Lysicamine
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Mefenamic Acid IP/BP/EP/USP Diclofenac Sodium IP/BP/EP/USP Ornidazole IP Diclofenac Potassium THOMAIND PAPER PH 2.0 TO 4.5 1 BOX BUFFER CAPSULE PH 9.2 - 10 CAP SODIUM CHLORIDE 0.1N CVS ALLOXAN MONOHYDRATE 98% PLATINUM 0.5% ON 3 MM ALUMINA PELLETS (TYPE 73) LITHIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
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