Taberdivarine H
Taberdivarine H is a natural product from Tabernaemontana officinalis.
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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.
Front Pharmacol.2021, 12:761922.
Nat Prod Sci.2016, 22(2)
LWT-Food Science and Technology2017, 75:488-496
Chemistry of Natural Compounds2018, 54(3):572-576
J Biomol Struct Dyn.2023, 1-21.
Free Radic Biol Med.2016, 97:307-319
Redox Rep.2024, 29(1):2392329.
J of Apicultural Research2020, 10.1080
Food Res Int.2022, 157:111207.
J of Pharmaceutical Analysis2020, doi: 10.1016
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Phytochemistry. 2015 Dec;120:46-52.
Cytotoxic indole alkaloids from Tabernaemontana officinalis.[Pubmed:
25687604 ]
METHODS AND RESULTS:
Continued interest in cytotoxic alkaloids resulted in the isolation of 37 alkaloids including 29 known monoterpenoid indole alkaloids from the aerial parts of Tabernaemontana officinalis. Of the remaining 8 alkaloids, six were bisindole alkaloids named taberdivarine A, taberdivarine B, taberdivarine C, taberdivarine D, taberdivarine E, taberdivarine F (1-6) and the two were monomers named taberdivarine G and Taberdivarine H (7-8).
CONCLUSIONS:
Alkaloids 1 and 2 are voaphylline-vobasinyl type bisindole alkaloids, a structural type previously unknown, while 3-6 exhibited cytotoxicity against three human cancer cell lines HeLa, MCF-7, and SW480 with IC50 values ranging from 1.42 to 11.35 μM.
