Natural Products from Panax japonicus var. major

Natural Products Isolated from Panax japonicus var. major

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.
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Natural Products from Panax japonicus var. major

10 natural product s associated with Panax japonicus var. major

Natural products and bioactive compounds from Panax japonicus var. major
Catalog No. Product Name CAS Number COA
BCN1079 20(R)-Protopanaxatriol
20(R)-Protopanaxatriol chemical structure
1453-93-6 COA
BCN2683 Chikusetsusaponin IV
Chikusetsusaponin IV chemical structure
7518-22-1 COA
BCN3432 Chikusetsusaponin IVa
Chikusetsusaponin IVa chemical structure
51415-02-2 COA
BCN1064 Ginsenoside Rb2
Ginsenoside Rb2 chemical structure
11021-13-9 COA
BCN1065 Ginsenoside Rb3
Ginsenoside Rb3 chemical structure
68406-26-8 COA
BCN1072 Ginsenoside Rc
Ginsenoside Rc chemical structure
11021-14-0 COA
BCN1075 Ginsenoside Rf
Ginsenoside Rf chemical structure
52286-58-5 COA
BCN5937 Ginsenoside Ro
Ginsenoside Ro chemical structure
34367-04-9 COA
BCN5616 Oleanolic acid
Oleanolic acid chemical structure
508-02-1 COA
BCN2794 Pseudoginsenoside RT1
Pseudoginsenoside RT1 chemical structure
98474-74-9 COA

References

[Transcriptome profiling and analysis of Panax japonicus var. major].[Pubmed: 26552161]


The rhizome of Panax japonicus var. major have been used as the natural medicinal agent by Chinese traditional doctors for more than thousand years. Most of the therapeutic effects of P. japonicus var. major had been reported due to the presence of tetracyclic or pentacyclic triterpene saponins. In this study, Illumina pair-end RNA-sequencing and de novo splicing were done in order to understand the pathway of triterpenoid saponins in this species. The valid reads data of 15. 6 Gb were obtained. The 62 240 unigenes were finally obtained by de novo splicing. After annotation, we discovered 19 unigenes involved in ginsenoside backbone biosynthesis. Additionally, 69 unigenes and 18 unigenes were predicted to have potential function of cytochrome P450 and UDP-glycosyltransferase based on the annotation results, which may encode enzymes responsible for ginsenoside backbone modification. This study provides global expressed datas for P. japonicus var. major, which will contribute significantly to further genome-wide research and analysis for this species.


[Chemical constituents of leaves of Panax japonicus var. major].[Pubmed: 25095375]


Seven compounds were isolated from the leaves of Panax japonicus var. major by chromatographic methods including silica gel, Sephadex LH-20, ODS and semi-preparative HPLC. Their structures were elucidated by their physical and chemical properties and spectral data analysis as 5, 7-dihydroxy-8-methoxyl flavone (1), ginsenoside Rs2 (2), quinquenoside R1 (3), ginsenoside Rs1 (4), notoginsenoside Fe (5), ginsenoside Rd2 (6) and gypenosiden IX (7). Among them, compound 1 was obtained from the Panax genus for the first time, and compounds 2-7 were isolated from this plant for the first time.


Bioactive constituents from the roots of Panax japonicus var. major and development of a LC-MS/MS method for distinguishing between natural and artifactual compounds.[Pubmed: 21417387]


Two new saponins, panajaponol (1) and pseudoginsenoside RT1 butyl ester (2), together with 35 known compounds (3-37), were isolated from the roots of Panax japonicus var. major. The structures of 1 and 2 were elucidated on the basis of spectroscopic analysis and chemical methods. Furthermore, a LC-MS/MS method was developed for confirming 2, 3, and 8 as natural compounds containing a butyl ester group. This method should be useful for distinguishing between minor natural and artifactual compounds in Panax species. Moreover, compounds 3, 6, 8, 9, 11, 13, and 15 exhibited strong inhibition of superoxide anion generation and elastase release by human neutrophils in response to formyl-l-methionyl-l-leucyl-l-phenylalanine/cytochalasin B (fMLP/CB), with IC(50) values ranging from 0.78 to 43.6 μM. In addition, 1 showed greater than 2- to 3-fold selective cytotoxic activity against KB and DU145 cancer cell lines.