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1-Hydroxy-N-methylacridone
1-Hydroxy-N-methylacridone
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 1-Hydroxy-N-methylacridone
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CAS No.: 16584-54-6
Catalog No.: CFN89268
Molecular Formula: C14H11NO2
Molecular Weight: 225.24 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The roots of Ruta chalepensis.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Biological Activity
Description: 1-Hydroxy-N-methylacridone is a natural product from Ruta chalepensis.
1-Hydroxy-N-methylacridone Description
Source: The roots of Ruta chalepensis.
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.

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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.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

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Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4397 mL 22.1985 mL 44.3971 mL 88.7942 mL 110.9927 mL
5 mM 0.8879 mL 4.4397 mL 8.8794 mL 17.7588 mL 22.1985 mL
10 mM 0.444 mL 2.2199 mL 4.4397 mL 8.8794 mL 11.0993 mL
50 mM 0.0888 mL 0.444 mL 0.8879 mL 1.7759 mL 2.2199 mL
100 mM 0.0444 mL 0.222 mL 0.444 mL 0.8879 mL 1.1099 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:
Phytochemistry, 1990, 29(12):3991-3992.
A moskachan from roots of Ruta chalepensis.[Reference: WebLink]
In addition to previously obtained coumarins and alkaloids, a group of additional coumarins, xanthatoxin, bergapten and rutolide as well as alkaloids graveolinine, 1-Hydroxy-N-methylacridone and two moskachans B and D together with the new moskachan, chalepimoskachan were isolated from a new collection of the roots of Ruta chalepensis.
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