Taibaihenryiins A
Taibaihenryiins A is a natural product from Rabdosia rubescens.
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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.
Biomol Ther (Seoul).2020, 28(6):542-548.
Phytomedicine.2022, 100:154036.
Journal of Mushroom2024, 22(4):192-198
Clin Transl Med.2021, 11(5):e392.
Korean j.of Pharm.2017, 70-76
Appl. Sci.2025, 15(1), 247
Cancers (Basel).2023, 15(1):293.
British Jou. Med.&Med. Research2014, 1802-1811
J Chromatogr A.2017, 1518:46-58
Int Immunopharmacol.2019, 71:361-371
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J Nat Prod. 2006 Apr;69(4):645-9.
7alpha,20-epoxy-ent-kauranoids from Isodon parvifolius.[Pubmed:
16643043 ]
METHODS AND RESULTS:
Nine new 7alpha,20-epoxy-ent-kaurane diterpenoids, parvifolines C-K (1-9), together with 12 known analogues, rabdoternin G (10), adenolin E (11), lasiodonin (12), lushanrubescensin F (13), parvifoliside (14), effusanin A (15), effusanin B (16), effusanin E (17), taibaihenryiin A (18), shikokianin (19), maoyecrystal J (20), and the acetonide of lasiodonin (21), were isolated from the leaves of Isodon parvifolius.
CONCLUSIONS:
The structures of compounds 1-9 were determined on the basis of spectroscopic methods including extensive 1D and 2D NMR analysis.
The new diterpenoids (1-9) and lasiodonin (12) were evaluated for their inhibitory activity against A549, HT-29, and K562 cell lines.
