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5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l-

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5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l- Suppliers list
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CAS:55610-01-0
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CAS:55610-01-0
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5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l- Basic information
Product Name:5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l-
Synonyms:5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l-;7-Methyl-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione;Cepharadione A;NSC 650435
CAS:55610-01-0
MF:C18H11NO4
MW:305.28
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Mol File:55610-01-0.mol
5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l- Structure
5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l- Chemical Properties
Melting point >350°C
Safety Information
MSDS Information
5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l- Usage And Synthesis
DescriptionThe callus tissue of Stephania cepharantha has provided a number of alkaloids that have been discovered and characterized by Japanese investigators. This base forms orange needles which melt above 350°C and possess a bright orange fluorescence. The ultraviolet spectrum has absorption maxima at 219, 238, 279, 290, 303, 315 and 439 nm with a shoulder at 265 nm. It belongs to the aporphine class and contains a methylenedioxy group and a methylimino group in the molecule.
UsesCepharadione A can be isolated from the roots of Piper betle Linn. Cepharadione A inhibits FMLP/CB induced elastase release by human neutrophils[1].
DefinitionChEBI: Cepharadione A is an isoquinoline alkaloid.
ReferencesAkasu, Itokawa, Fujita, Tetrahedron Lett., 3609 (1974)
5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline-5,6(7H)-dione, 7-methy l- Preparation Products And Raw materials
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