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2-O-Methylanigorufone
2-O-Methylanigorufone
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 2-O-Methylanigorufone
Price:
CAS No.: 56252-05-2
Catalog No.: CFN96873
Molecular Formula: C20H14O2
Molecular Weight: 286.33 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source: The whole plants of Monochoria vaginalis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Biological Activity
Description: 2-O-Methylanigorufone is a natural product from Monochoria vaginalis.
In vitro:
Planta Medica, 2013, 79(13).
Phytochemical constituents of Monochoria vaginalis var. plantaginea and their antioxidative and cytotoxic activities[Reference: WebLink]
The aquatic plant Monochoria vaginalis var. plantaginea (Roxb.) Solms (Pontederiaceae) is a traditional herbal medicine, and widely distributed in Asian countries including Korea, China, Japan, India, and Malaysia. The whole plant is considered as a functional food and has also been used for treatment of dysentery, enteritis, acute tonsillitis, gum abscesses, erysipelas, boils. Juice of the leaves is taken for coughs and that of the root for stomach and liver complaints, asthma and toothache.
METHODS AND RESULTS:
In our continuing studies to find bioactive compounds from natural products, several structures were isolated from the whole plant of Monochoria vaginalis var. plantaginea. Among five fractions of the MeOH extract, the n-hexane fraction exhibited comparatively higher antioxidative and cytotoxic activities than the other fractions. The CH2Cl2 and BuOH fractions also showed strong antioxidative activity. Ten compounds were isolated from the n-hexane and CH2Cl2 fractions, and their structures were identified as cholest-4-en-3,6-dione, stigmast-4-ene-3,6-dione, methoxyanigorufone(2-O-Methylanigorufone), (10Z)-1-(2,6-dihydroxyphenyl)octadec-10-en-1-one, 1-(4-methoxyphenyl)-7-phenyl-(6E)-6-hepten-3-one, (+)-dehydrovomifoliol, 4-hydroxyphenylacetonitrile, (6R,9S)-vomifoliol, (6S,9S)-vomifoliol, (3S,5R,6R,7E,9R)-5,6-epoxy-3,9-dihydroxy-7-megastigmene by comparison of their spectral data with literature values. Cytotoxic and antioxidative activities for solvent fractions and isolated compounds were evaluated using SRB (sulforhodamin B) assay against human tumor cell lines (A549, SK-OV-3, SK-MEL-2, and HCT15), and ORAC (oxygen radical absorbance capacity) assay, respectively.
2-O-Methylanigorufone Description
Source: The whole plants of Monochoria vaginalis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
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IF=36.216(2019)

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Cell Metab. 2020 Mar 3;31(3):534-548.e5.
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IF=22.415(2019)

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IF=13.903(2019)

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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.4925 mL 17.4624 mL 34.9247 mL 69.8495 mL 87.3118 mL
5 mM 0.6985 mL 3.4925 mL 6.9849 mL 13.9699 mL 17.4624 mL
10 mM 0.3492 mL 1.7462 mL 3.4925 mL 6.9849 mL 8.7312 mL
50 mM 0.0698 mL 0.3492 mL 0.6985 mL 1.397 mL 1.7462 mL
100 mM 0.0349 mL 0.1746 mL 0.3492 mL 0.6985 mL 0.8731 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Records of Natural Products, 2010, 4(1).
Phenylphenalenones from Musa cv. ‘Thepanom’ (BBB).[Reference: WebLink]
Chemical constituents of Musa cv. ‘Thepanom’ (BBB) or "praying hands" banana (Musaceae) were investigated by means of chromatographic techniques.
METHODS AND RESULTS:
A new natural product of the phenylphenalenone type, 3-hydroxy-4-phenyl-1H,3H-benzo[de]isochromen-1-one, and two known natural products, methoxyanigorufone(2-O-Methylanigorufone) and isoanigorufone, were isolated and identified by NMR spectroscopy and mass spectrometry. Additionally, by HPLC analysis, three condensed dimeric phenylphenalenones, namely anigorootin, 4′-hydroxyanigorootin, 4',4''-Dihydroxyanigorootin, were identified.
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