Indaconitine
Indaconitine is a natural product from Aconitum hemsleyanum PRITZ.
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.
J of Dentistry & Oral Health2019, 2641-1962
Int J Mol Sci.2022, 23(20):12516.
Food Chem.2024, 458:140201.
J of l. Chroma.&Related Tech2020, 43(11-12):414-423.
Appl. Sci.2020, 10(20),7374.
Nutrients.2020, 12(12):3638.
Biomed Pharmacother.2020, 125:109784.
Antioxidants (Basel).2023, 12(12):2131.
ACS Synth Biol.2020, 9(9):2282-2290.
Int J Med Sci.2021, 18(10):2155-2161.
Related and Featured Products
Chem Pharm Bull (Tokyo). 2003 May;51(5):592-4.
Hemsleyatine, a novel C19-diterpenoid alkaloid with 8-amino group from Aconitum hemsleyanum.[Pubmed:
12736463]
The new compound hemsleyatine (1) was isolated along with four known C(19)-diterpenoid alkaloids: Indaconitine (4), yunaconitine (5), chasmanine (6), and talatisamine (7) from the roots of Aconitum hemsleyanum PRITZ.
METHODS AND RESULTS:
Structures were established by spectral analysis, including tow dimeusional (2D) NMR spectroscopy and a chemical method. Hemsleyatine (1) is the first C(19)-diterpenoid alkaloid bearing the 8-amino group. In addition, the assignments of some (13)C signals for pseudaconine (3) were revised by comparison with those of hemsleyatine (1).
