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Fortuneine
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Product Name Fortuneine
Price:
CAS No.: 87340-25-8
Catalog No.: CFN96760
Molecular Formula: C20H25NO3
Molecular Weight: 327.42 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The twigs and leaves of Cephalotaxus fortunei.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Biological Activity
Description: Fortuneine is a natural product from Cephalotaxus fortunei.
Fortuneine Description
Source: The twigs and leaves of Cephalotaxus fortunei.
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.
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)

PMID: 28005066

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 3.0542 mL 15.2709 mL 30.5418 mL 61.0836 mL 76.3545 mL
5 mM 0.6108 mL 3.0542 mL 6.1084 mL 12.2167 mL 15.2709 mL
10 mM 0.3054 mL 1.5271 mL 3.0542 mL 6.1084 mL 7.6355 mL
50 mM 0.0611 mL 0.3054 mL 0.6108 mL 1.2217 mL 1.5271 mL
100 mM 0.0305 mL 0.1527 mL 0.3054 mL 0.6108 mL 0.7635 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, 1983, 22(1):251-253.
Fortuneine, a homoerythrina alkaloid from cephalotaxus fortunei.[Reference: WebLink]

METHODS AND RESULTS:
Examination of the weakly basic fraction of the twigs and leaves of Cephalotaxus fortunei, a plant native to China, has resulted in the isolation and characterization of epiwilsonine, wilsonine and a new alkaloid named Fortuneine.
CONCLUSIONS:
The structure of Fortuneine was deduced by spectral and chemical means. In addition, epiFortuneine was prepared and spectral data collected.
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