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6-Acetonyl-N-methyl-dihydrodecarine
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Product Name 6-Acetonyl-N-methyl-dihydrodecarine
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CAS No.: 1253740-09-8
Catalog No.: CFN99367
Molecular Formula: C23H21NO5
Molecular Weight: 391.4 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Yellow powder
Source: The fruits of Evodia rutaecarpa
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
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Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: 6-Acetonyl- N -methyl-dihydrodecarine has mosquito larvicidal activity against the malaria vector Anopheles gambiae.
Targets: Antifection
In vitro:
Pesticide Biochem. Physiol., 2011, 99(1):82-5.
Mosquito larvicidal activity of alkaloids from Zanthoxylum lemairei against the malaria vector Anopheles gambiae[Reference: WebLink]

METHODS AND RESULTS:
Four alkaloids, 10-O-demethyl-17-O-methylisoarnottianamide 1, 6-Acetonyl-N-methyl-dihydrodecarine 2, nitidine 3, and chelerythrine 4 were isolated from the plant Zanthoxylum lemairei (Rutaceae) and evaluated for mosquito larvicidal activity against the malaria vector Anopheles gambiae. The mortalities of the larvae were determined after 24 h. The results of the larvicidal tests demonstrated that compounds 1 and 2 were the most potent with mortality rates of 96.7% and 98.3% at a concentration of 250 mg/L, respectively. Compound 3 was less potent with a mortality of 28.3% at the same concentration. The percent mortality of 100% was observed at a concentration of 500 mg/L. The least potent of the four alkaloids was compound 4, which achieved 100% mortality at 1000 mg/L.
CONCLUSIONS:
These findings could be useful in the research for newer more selective, biodegradable and natural larvicidal compounds or can be used as lead compounds for the development of larvicides.
6-Acetonyl-N-methyl-dihydrodecarine Description
Source: The fruits of Evodia rutaecarpa
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.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5549 mL 12.7747 mL 25.5493 mL 51.0986 mL 63.8733 mL
5 mM 0.511 mL 2.5549 mL 5.1099 mL 10.2197 mL 12.7747 mL
10 mM 0.2555 mL 1.2775 mL 2.5549 mL 5.1099 mL 6.3873 mL
50 mM 0.0511 mL 0.2555 mL 0.511 mL 1.022 mL 1.2775 mL
100 mM 0.0255 mL 0.1277 mL 0.2555 mL 0.511 mL 0.6387 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:
J. Braz. Chem. Soc, 2009,20(2): 379-382.
Fernandes CC et al. 6-acetonyl-N-methyl-dihydrodecarine, a new alkaloid from Zanthoxylum riedelianum. [Reference: WebLink]

METHODS AND RESULTS:
A new benzophenanthridine alkaloid, 6-Acetonyl-N-methyl-dihydrodecarine was isolated from Zanthoxylum riedelianum roots together with lupeol, 6-acetonyldihydrochelerythrine and 6-acetonyldihydroavicine. The structures were established from the IR, MS and NMR spectral data, including 2D-NMR experiments.
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