Stelleranol
Stelleranol shows potent in vitro antiviral activity against respiratory syncytial virus (RSV).
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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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Chin Med. 2010 Jun 21;5:23.
Antiviral biflavonoids from Radix Wikstroemiae (Liaogewanggen).[Pubmed:
20565950 ]
Radix Wikstroemiae is a common Chinese herbal medicine. The ethyl acetate fraction of the ethanolic extract of W. indica possesses potent in vitro antiviral activity against respiratory syncytial virus (RSV). This study aims to identify the antiviral components of the active fraction.
METHODS AND RESULTS:
The active fraction of the Radix Wikstroemiae extract was isolated with chromatographic methods such as silica gel, Sephadex LH-20 and semi-preparative high performance liquid chromatography (HPLC) columns. The structures of the isolated compounds were determined based on spectroscopic analyses. The in vitro antiviral activity of the compounds against RSV was tested with the cytopathic effect (CPE) reduction assay and the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. Four biflavonoids, namely neochamaejasmin B, genkwanol B, Genkwanol C and Stelleranol, were isolated and characterized. Genkwanol B, Genkwanol C and Stelleranol, which are stereo isomers of spirobiflavonoids, showed potent anti-RSV activity whereas neochamaejasmin B did not.
CONCLUSIONS:
Neochamaejasmin B, genkwanol B, Genkwanol C and Stelleranol were isolated from Radix Wikstroemiae and the complete absolute configurations of five chiral carbons in Stelleranol were substantiated for the first time. Furthermore, the anti-RSV activity of genkwanol B, Genkwanol C and Stelleranol was reported for the first time.
Nat Prod Commun. 2016 Apr;11(4):475-6.
Chemical Constituents from the Roots, Stems and Leaves of Diplomorpha sikokiana.[Pubmed:
27396196]
METHODS AND RESULTS:
Four diarylpentanoids (1-4), two phenylpropanoids (5-6), three biflavonoids (7-9), two lignans (10-11) and a coumarin (12) were isolated from the roots of Diploniorpha sikokiana (Franchet & Savatier) Honda (Family: Thymelaeaceae). Similarly, two phenylpropanoids (5-6), five biflavonoids (7-9, 13, 14), three lignans (11, 15, 16), a flavonoid (17) and two coumarins (12, 18) were isolated from the stems, and five flavonoids (17, 19-22) from the leaves.
CONCLUSIONS:
Among them, 1,5-diphenyl-l-pentanone (1), 1,5-diphenyl-2-penten-l-one (2), 3(S)-hydroxy-1,5-diphenylpentane (3), Stelleranol (8), (-)-syringaresinol (10), (-)-pinoresinol 4,4'-di-O-β-D-glucopyranoside (11), apiosylskimmin (12), syringaresinol 4-O-β-D-glucopyranoside (16), quercetin 3-O-α-L-rhamnopyranoside (19), kaempferol 3-0-α-L-rhamnopyranoside (20) and tiliroside (21) were isolated for the first time from D. sikokiana.
