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Natural Products from Aconitum carmichaelii

Natural Products Isolated from Aconitum carmichaelii

BioCrick provides high-purity natural products and bioactive compounds isolated and purified from natural sources for scientific research.

  • Natural product compounds selected from diverse chemical and biological sources.
  • Broad structural diversity and coverage of biological activities.
  • Product activity information can be supported by published literature, patents and research reports.
  • Natural products can be selected according to source, target, activity and disease research interests.
  • Compounds should be stored according to the product specifications after receipt.
Natural products isolated from Aconitum carmichaelii
Natural products isolated from Aconitum carmichaelii

Natural Products from Aconitum carmichaelii

22 natural product s associated with Aconitum carmichaelii

Natural products and bioactive compounds from Aconitum carmichaelii
Catalog No. Product Name CAS Number COA
BCN2800 12-Epinapelline
12-Epinapelline chemical structure
110064-71-6 COA
BCN2797 3-Deoxyaconitine
3-Deoxyaconitine chemical structure
3175-95-9 COA
BCN2394 Aconine
Aconine chemical structure
509-20-6 COA
BCN1014 Aconitine
Aconitine chemical structure
302-27-2 COA
BCN5400 Benzoylaconine
Benzoylaconine chemical structure
466-24-0 COA
BCN2821 Benzoylhypacoitine
Benzoylhypacoitine chemical structure
63238-66-4 COA
BCN5398 Benzoylmesaconine
Benzoylmesaconine chemical structure
63238-67-5 COA
BCN2375 Bullatine B
Bullatine B chemical structure
466-26-2 COA
BCN2516 Crassicauline A
Crassicauline A chemical structure
79592-91-9 COA
BCN5404 Deltaline
Deltaline chemical structure
6836-11-9 COA
BCN5406 Denudatine
Denudatine chemical structure
26166-37-0 COA
BCC8317 DL-Demethylcoclaurine
DL-Demethylcoclaurine chemical structure
5843-65-2 COA
BCN5948 Ferulic acid
Ferulic acid chemical structure
1135-24-6 COA
BCN9073 Ferulic Acid Methyl Ester
Ferulic Acid Methyl Ester chemical structure
2309-07-1 COA
BCN2822 Fuziline
Fuziline chemical structure
80665-72-1 COA
BCN1001 Honokiol
Honokiol chemical structure
35354-74-6 COA
BCN5988 Hypaconitine
Hypaconitine chemical structure
6900-87-4 COA
BCN6259 Indaconitine
Indaconitine chemical structure
4491-19-4 COA
BCC8331 Karakoline
Karakoline chemical structure
39089-30-0 COA
BCN5987 Mesaconitine
Mesaconitine chemical structure
2752-64-9 COA
BCN2536 Napellonine
Napellonine chemical structure
509-24-0 COA
BCN4211 Uracil
Uracil chemical structure
66-22-8 COA

References

The influences of thermal processing on phytochemicals and possible routes to the discovery of new phytochemical conjugates.[Pubmed: 29787299]


In our diets, many of the consumed foods are subjected to various forms of heating and thermal processing. Besides enhancing the taste, texture, and aroma of the foods, heating helps to sterilize and facilitate food storage. On the other hand, heating and thermal processing are frequently reported during the preparation of various traditional herbal medicines. In this review, we intend to highlight works by various research groups which reported on changes in phytochemicals and bioactivities, following thermal processing of selected plant-derived foods and herbal medicines. Relevant cases from plant-derived foods (garlic, coffee, cocoa, barley) and traditional herbal medicines (Panax ginseng, Polygonum multiforum, Aconitum carmichaelii Debeaux, Angelica sinensis Radix) will be presented in this review. Additionally, related works using pure phytochemical compounds will also be highlighted. In some of these cases, the amazing formation of new compounds were being reported. Maillard reaction could be concluded as the predominant pathway leading to the formation of new conjugates, along with other possibilities being suggested (degradation, transglycosylation, deglycosylation and dehydration). With collective efforts from all researchers, it is hoped that more details will be revealed and lead to the possible discovery of new, heat-mediated phytochemical conjugates.


Four New Diterpenoid Alkaloids from the Roots of Aconitum carmichaelii.[Pubmed: 29785743]


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Qualitative and quantitative analysis of lipo-alkaloids and fatty acids in Aconitum carmichaelii using LC-MS and GC-MS.[Pubmed: 29603449]


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New dianthramide and cinnamic ester glucosides from the roots of Aconitum carmichaelii.[Pubmed: 29597834]


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