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ChemicalBook >  Product Catalog >  Natural Products >  Alkaloids >  5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl-

5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl-

Basic information Safety Supplier Related

5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl- Basic information

Product Name:
5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl-
Synonyms:
  • 5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl-
  • DEHYDROCREBANINE
CAS:
77784-22-6
MF:
C20H19NO4
MW:
337.37
Mol File:
77784-22-6.mol
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5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl- Chemical Properties

Boiling point:
547.6±50.0 °C(Predicted)
Density 
1.312±0.06 g/cm3(Predicted)
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
powder
pka
2.83±0.20(Predicted)
color 
Yellow
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5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl- Usage And Synthesis

Occurrence

A constituent of the basic extract of Stephania sasakii, this derivative of crebanine has been obtained as colourless crystals from EtOH.

Uses

Dehydrocrebanine is an alkaloid that can be isolated from the tuber and leaves of Stephania venosa. Dehydrocrebanine has in vitro anti-cancer activity[1].

target

Antifection

References

[1] Makarasen A, et al. Cytotoxic and antimicrobial activities of aporphine alkaloids isolated from Stephania venosa (Blume) Spreng. Planta Med. 2011 Sep;77(13):1519-24. DOI:10.1055/s-0030-1270743

5H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline, 6,7-dihydro-9,10-dime thoxy-7-methyl-Supplier

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