Momordicine V

Momordicine V
Product Name Momordicine V
CAS No.: 1012315-36-4
Catalog No.: CFN95164
Molecular Formula: C39H60O12
Molecular Weight: 720.9 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The fruits of Momordica charantia
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $463/5mg
Momordicine V can deter significantly the oviposition by L. trifolii on host plant leaves treated at 26.16 microg/cm2 leaf surface.
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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

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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  • J Pharm Biomed Anal.2022, 207:114398.
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  • Int J Mol Sci.2019, 20(8):E1855
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  • Food Funct.2024, 15(4):1852-1866.
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    Z Naturforsch C. 2007 Jul-Aug;62(7-8):603-7.
    A new oviposition deterrent to the leafminer, Liriomyza trifolii: cucurbitane glucoside from Momordica charantia.[Pubmed: 17913080 ]

    METHODS AND RESULTS:
    A new cucurbitane glucoside, 23-O-beta-D-glucopyranosyl-7-hydroxy-3-O-malonylcucurbita-5,24-dien-19-al, named Momordicine V, has been isolated from Momordica charantia leaves, along with the previously reported compounds, momordicine I, momordicine II, momordicine IV and 3-O-malonylmomordicine I. The structure of the new compound was established on the basis of spectral analysis, as well as by its conversion to momordicine II by alkaline catalyzed hydrolysis.
    CONCLUSIONS:
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