(-)-Hydroxydihydrobovolide
(-)-Hydroxydihydrobovolide is a natural product from Clausena emarginata Huang.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Asian J Beauty Cosmetol2020, 18(3): 265-272.
Biol Pharm Bull.2021, 44(12):1891-1893.
Biomed Chromatogr.2019, 8:e4774
J of Pharmaceutical Analysis2020, doi: 10.1016
Konkuk University2023, 29:4634721
Heliyon2022, 8(2):e08866.
J Health Sci Med Res.2023, 31584.
Horticulture Research2023, uhad164.
NanoBioScience2024, v13:3:115.
Molecules.2023, 28(7):3039.
Related and Featured Products
J Nat Prod. 2001 Jun;64(6):772-7.
Antimalarial compounds from Rhaphidophora decursiva.[Pubmed:
11421741]
METHODS AND RESULTS:
Bioassay-directed fractionation led to the isolation of 14 compounds, six of which possess antimalarial activity, from the dried leaves and stems of Rhaphidophora decursiva. Polysyphorin (1) and rhaphidecurperoxin (6) showed strong activities against Plasmodium falciparum. Rhaphidecursinol A (2), rhaphidecursinol B (3), grandisin (4), and epigrandisin (5) were less active against the same organism. Among the isolates, rhaphidecursinol A (2) and rhaphidecursinol B (3) were determined to be new neolignans, and rhaphidecurperoxin (6) is a new benzoperoxide.
CONCLUSIONS:
Known compounds isolated include polysyphorin (1), grandisin (4), epigrandisin (5), (+)-medioresinol, (-)-pinoresinol, (-)-syringaresinol, (+)-glaberide I, (+)-dehydrovomifoliol, (-)-liliolide, (-)-Hydroxydihydrobovolide, and N-butylbenzamide, of which compound 1 appears worthy of further evaluation as an antimalarial agent.
Structure elucidation and identification were accomplished by spectroscopic means including 1D and 2D NMR analyses.
