8-Deacetylyunaconitine
8-Deacetylyunaconitine is a natural product from Aconitum Vilmorinian Radix.
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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.
Kor. J. Pharmacogn.2016, 47(1):62-72
Regul Toxicol Pharmacol.2023, 142:105433.
J Biochem Mol Toxicol.2021, 35(5):e22731.
Phytomedicine.2024, 126:155442.
Toxicological Research2020, doi: 10.1007.
European Journal of Integrative Medicine2018, 20:165-172
Heliyon.2023, e12778.
J Chromatogr B Analyt Technol Biomed Life Sci.2018, 1080:27-36
Evid Based Complement Alternat Med.2016, 2016:1230294
Biochem Biophys Res Commun.2017, 482(4):1095-1101
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Zhong Yao Cai. 2015 May;38(5):988-91.
Chemical Constituents from Processed Products of Aconitum Vilmoriniani Radix.[Pubmed:
26767293]
To investigate the chemical constituents of the processed products of Aconitum Vilmorinian Radix.
METHODS AND RESULTS:
The constituents were isolated by repeated column chromatography over silica gel, alumina and RP-C18 as well as recrystallization. The structures were elucidated on the basis of spectral analysis and physicochemical properties.
Ten compounds were obtained from the methanol extract, and they were identified as yunaconitine (1), 8-deacetyl-yunaconitine (2), geniculatine C (3), vilmorrianine B (4), vilmorrianine C(5), vilmorrianine D (6), talatisamine (7), β-sitosterol (8), β-daucosterol (9) and β-sitosterol acetate (10).
CONCLUSIONS:
All compounds are obtained from the processed products of Aconitum Vilmoriniani Radix for the first time.
J Sep Sci. 2013 Aug;36(16):2680-5.
Accelerated solvent extraction and pH-zone-refining counter-current chromatographic purification of yunaconitine and 8-deacetylyunaconitine from Aconitum vilmorinianum Kom.[Pubmed:
23784883]
METHODS AND RESULTS:
This study aimed to seek an efficient method to extract and purify yunaconitine and 8-Deacetylyunaconitine from Aconitum vilmorinianum Kom. by accelerated solvent extraction combined with pH-zone-refining counter-current chromatography.
The major extraction parameters for accelerated solvent extraction were optimized by an orthogonal test design L9 (3)(4). Then a separation and purification method was established using pH-zone-refining counter-current chromatography with a two-phase solvent system composed of petroleum ether/ethyl acetate/methanol/water (5:5:2:8, v/v) with 10 mM triethylamine in the upper phase and 10 mM HCl in the lower phase. From 2 g crude extract, 224 mg of 8-Deacetylyunaconitine (I) and 841 mg of yunaconitine (II) were obtained with a purity of over 98.0%.
CONCLUSIONS:
The chemical structures were identified by ESI-MS and (1)H and (13)C NMR spectroscopy.
