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Natural Products from Paliurus ramosissimus

Natural Products Isolated from Paliurus ramosissimus

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Natural Products from Paliurus ramosissimus

8 natural product s associated with Paliurus ramosissimus

Natural products and bioactive compounds from Paliurus ramosissimus
Catalog No. Product Name CAS Number COA
BCN5582 Bergapten
Bergapten chemical structure
484-20-8 COA
BCN1249 Betulinaldehyde
Betulinaldehyde chemical structure
13159-28-9 COA
BCN5524 Betulinic acid
Betulinic acid chemical structure
472-15-1 COA
BCN9028 Byakangelicin
Byakangelicin chemical structure
482-25-7 COA
BCN1209 Eriodictyol
Eriodictyol chemical structure
552-58-9 COA
BCN5568 Isopimpinellin
Isopimpinellin chemical structure
482-27-9 COA
BCN2590 Poncirin
Poncirin chemical structure
14941-08-3 COA
BCN4881 Xanthotoxol
Xanthotoxol chemical structure
2009-24-7 COA

References

[Triterpenes from fruits of Paliurus ramosissimus].[Pubmed: 19806894]


To study the chemical constituents of the fruits of Paliurus ramosissimus, various chromatographic techniques were used to separate and purify the chemical constituents. Three triterpenes have been isolated and purified by using various column chromatography. Their structures were elucidated by their physico-chemical properties and spectroscopic data. These compounds were determined as: 22S, 23R-epoxy-tirucalla-7-ene-3alpha,24, 25-triol (1), 21S, 23R-epoxy-21, 24S, 25-trihydroxy-apotirucalla-7-ene-3-one (2), 21R, 23R-epoxy-21-ethoxy-24S, 25-dihydroxy-apotirucalla-7-ene-3-one (3), separately. Compound 1 is a new compound, and the others were obtained from this genus for the first time.


[Studies on chemical constituents from fruits of Paliurus ramosissimus].[Pubmed: 17357553]


To study the chemical constituents from the fruits of Paliurus ramosissimus.


Calculating three-dimensional molecular structure of paliurine B from atom-atom distance and restrained energy minimization.[Pubmed: 8461326]


The conformation of paliurine B, a 13-membered cyclopeptide alkaloid isolated from Paliurus ramosissimus, has been determined from 2D NMR and distance geometry, followed by the restrained energy minimization calculation. The conformation of the 13-membered ring is well-defined but that of the acyclic dipeptide tail region is relatively disordered. In addition, the cavity in the 13-membered ring is just large enough to insert a magnesium ion but is a little small for calcium or sodium ions.