Drahebenine
Drahebenine is a natural product from Daphniphyllum longeracemosum.
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.
Inflammation2015, 38(1):445-55
Int J Mol Sci.2024, 25(2):764.
In Vivo.2022, 36(3):1136-1143.
Food Sci Biotechnol.2023, 32(9):1215-1223.
bioRxiv - Molecular Biology2023, 535548.
J Pharm Biomed Anal.2016, 129:50-59
Phytochemistry.2017, 141:162-170
Molecules.2020, 25(15):3353.
Natural Product Communications2020, doi: 10.1177.
Journal of Food Hygiene and Safety2019, 34(5):413-420
Related and Featured Products
Phytochemistry. 2012 Oct;82:166-71.
Phenolic alkaloids from the aerial parts of Dracocephalum heterophyllum.[Pubmed:
22800911 ]
METHODS AND RESULTS:
Chemical examination of aerial parts of Dracocephalum heterophyllum resulted in isolation of phenolic alkaloids, including two flavonoidal alkaloids, drahebephins A and B, one imidazole alkaloid with a phenolic substituent, Drahebenine, together with 15 other known compounds. Their structures were established by extensive spectroscopic data analyses. Due to the stereogenic center in the pyrrolidin-2-one ring, the flavonoidal alkaloids are chiral, although they were isolated as racemates. The enantiomers were separated by HPLC using a chiral phase and stereochemically characterized by circular dichroism (CD) spectroscopy.
CONCLUSIONS:
The structure of compound Drahebenine was established by X-ray crystallography.