| Weight | 342.415 g/mol |
|---|---|
| Formula | C20H24NO4+ |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Magnoflorine (2141-09-5)
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- Molecular Cloning and Characterization of CYP80G2, a Cytochrome P450 That Catalyzes an Intramolecular CC Phenol Coupling of (S)-Reticuline in Magnoflorine Biosynthesis, from Cultured Coptis japonica Cells (Journal of Biological Chemistry, 2008)
- Magnoflorine from Coptidis Rhizoma Protects High Density Lipoprotein during Oxidant Stress (Biological & Pharmaceutical Bulletin, 2007)
- Magnoflorine from Tinospora cordifolia stem inhibits -glucosidase and is antiglycemic in rats (Journal of Functional Foods, 2012)
- Analytical methods for determination of magnoflorine and saponins from roots of Caulophyllum thalictroides (L.) Michx. Using UPLC, HPLC and HPTLC (Journal of Pharmaceutical and Biomedical Analysis, 2011)
- Protective effect of magnoflorine isolated from coptidis rhizoma on Cu2+-induced oxidation of human low density lipoprotein. (Planta Medica, 2007)
- The involvement of magnoflorine in the sedative and anxiolytic effects of Sinomeni Caulis et Rhizoma in mice (Journal of Natural Medicines, 2013)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C
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InChIKeyYLRXAIKMLINXQY-UHFFFAOYSA-O
- Pubchem - Magnoflorine
- Wikipedia - Magnoflorine
Magnoflorine is a chemical compound isolated from the rhizome of Sinomenium acutum and from Pachygone ovata. It is classified as an aporphine alkaloid.
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Magnoflorine
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