Isochandalone
Isochandalone is a natural product from Derris robusta.
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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.
Food Control2022, 132:108434.
Int J Mol Sci.2018, 19(2)
Oxid Med Cell Longev.2021, 2021:4883398.
Nutraceutical Research . 2021, 19(1),p90-105.
Separations2023, 10(7), 411.
Drug Dev Res.2020, doi: 10.1002
Biomed Pharmacother.2024, 171:116166.
Plant Physiol.2023, 193(3):1758-1771.
Chem Biol Interact.2024, 403:111249.
VNU Journal of Science: Med.& Pharm. Sci.2022, 38(2):2588-1132.
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Z Naturforsch C. 2002 Jul-Aug;57(7-8):609-13.
A new prenylisoflavone from Ulex jussiaei.[Pubmed:
12240984]
METHODS AND RESULTS:
A new naturally occurring isoflavone, derrone, was isolated from Ulex jussiaei (Leguminosae) together with the isoflavones ulexins A-C, lupalbigenin, isolupalbigenin, 7-O-methylso-lupalbigenin, isoderrone, ulexone A and Isochandalone, the pterocarpans (6aR,11aR)-(-)-maackiain, (6aR,11aR)-(-)-2-methoxymaackiain and (6aR,11aR)-(-)-4-methoxymaackiain, the chalcone 4-hydroxylonchocarpine and the dihydrochalcone crotaramosmine.
CONCLUSIONS:
The antifungal activity of the new compound was tested by a bioautographic method against Cladosporium cucumerinum, and as expected from structural features it proved to have no activity.
