Natural Products from Lonicera japonica

Natural Products Isolated from Lonicera japonica

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 from Lonicera japonica

32 natural product s associated with Lonicera japonica

Natural products and bioactive compounds from Lonicera japonica
Catalog No. Product Name CAS Number COA
BCN2633 5-Isopropyl-2-methylphenol
5-Isopropyl-2-methylphenol chemical structure
499-75-2 COA
BCN5159 alpha-Hederin
alpha-Hederin chemical structure
27013-91-8 COA
BCN1015 Beta-Sitosterol
Beta-Sitosterol chemical structure
83-46-5 COA
BCN5979 Caffeic acid
Caffeic acid chemical structure
331-39-5 COA
BCN3181 Campesterol
Campesterol chemical structure
474-62-4 COA
BCN5906 Chlorogenic acid
Chlorogenic acid chemical structure
327-97-9 COA
BCN5907 Cryptochlorogenic acid
Cryptochlorogenic acid chemical structure
905-99-7 COA
BCN9087 Cyclohexanecarboxylic acid, 3-[[(2E)-3-[4-(D-glucopyranosyloxy)-3-hydroxyphenyl]-1-oxo-2-propen-1-yl...
Cyclohexanecarboxylic acid, 3-[[(2E)-3-[4-(D-glucopyranosyloxy)-3-hydroxyphenyl]-1-oxo-2-propen-1-yl... chemical structure
1629852-63-6 COA
BCN4993 Diosimin
Diosimin chemical structure
520-27-4 COA
BCN5328 Diosmetin-7-O-beta-D-glucopyranoside
Diosmetin-7-O-beta-D-glucopyranoside chemical structure
20126-59-4 COA
BCN5940 Dipsacoside B
Dipsacoside B chemical structure
33289-85-9 COA
BCN5964 Eugenol
Eugenol chemical structure
97-53-0 COA
BCN5948 Ferulic acid
Ferulic acid chemical structure
1135-24-6 COA
BCN5513 Hederagenin
Hederagenin chemical structure
465-99-6 COA
BCN5654 Hesperidin
Hesperidin chemical structure
520-26-3 COA
BCN5570 Hyperoside
Hyperoside chemical structure
482-36-0 COA
BCN5908 Isochlorogenic acid A
Isochlorogenic acid A chemical structure
2450-53-5 COA
BCN5569 Isoquercitrin
Isoquercitrin chemical structure
482-35-9 COA
BCN5551 Isorhamnetin
Isorhamnetin chemical structure
480-19-3 COA
BCN5944 Liquiritin
Liquiritin chemical structure
551-15-5 COA
BCN1153 Loganin
Loganin chemical structure
18524-94-2 COA
BCN5600 Luteolin
Luteolin chemical structure
491-70-3 COA
BCN5388 Luteolin-7-O-glucoside
Luteolin-7-O-glucoside chemical structure
5373-11-5 COA
BCN5009 Morroniside
Morroniside chemical structure
25406-64-8 COA
BCN4450 Neochlorogenic acid
Neochlorogenic acid chemical structure
906-33-2 COA
BCN5616 Oleanolic acid
Oleanolic acid chemical structure
508-02-1 COA
BCN1206 Palmitic acid
Palmitic acid chemical structure
57-10-3 COA
BCN6049 Quercetin
Quercetin chemical structure
117-39-5 COA
BCN1112 Rhoifolin
Rhoifolin chemical structure
17306-46-6 COA
BCN5800 Secoxyloganin
Secoxyloganin chemical structure
58822-47-2 COA
BCN6219 Sweroside
Sweroside chemical structure
14215-86-2 COA
BCN6059 Syringin
Syringin chemical structure
118-34-3 COA

References

[Comparative Analysis of Different Strains of Lonicera japonica on Appearance and Internal Quality].[Pubmed: 30088873]


To provide the reference for germplasm identification and breeding of Lonicera japonica.


[Chemical fingerprinting and similarity analysis of Lonicera japonica resources].[Pubmed: 29950078]


LC-MS was used to detect 41 population of Lonicera japonica from different areas. LC-MS chemical chromatographic profile has been established. There were 23 common peaks, seventeen of which were identified according to reference standard and reference; SPSS software was applied to calculate the similarity of chemical fingerprints of 41 batches and the range was from 0.99 to 0.12. On this basis, the L. japonica's metabolites consistency was classified. Combined with comprehensive analysis of genetic identity, we can provide a theoretical basis for the authenticity research of Dao-di herbs and reference information for the breeding of excellent L. japonica.


[Establishment of DNA identity card and analysis of genetic similarity among 58 varieties in Lonicera japonica].[Pubmed: 29902892]


A total of 58 varieties in Lonicera japonica from 20 producing areas were amplified by 22 pairs of SSR primers. Seven pairs of polymorphic primers were screened and their primers were used to establish DNA identity card and analyze genetic similarity.All the 58 varieties could be distinguished each other by the DNA identity card constituted by 7 pairs of core SSR primers.The genetic similarity coefficients of 58 varieties ranged from 0.366 7 to 0.916 7 by using PopGene32(vesion1.32). Furthermore, all the varieties consistency were classified into 4 groups and constructed an evaluation table according to cluster analysis by an un-weighted pair-group average method with arithmetic mean. As expected, the results of cluster and evaluation table reflected 58 varieties relatives, which provide reference information for the selection of fine germplasm of L. japonica and the theoretical basis for the study of Dao-di herbs.


Bioactive luteoloside produced by Myroides odoratimimus, solvent-tolerant bacterium form the rhizosphere of Lonicera japonica.[Pubmed: 29882431]


Luteoloside (luteolin-7-O-glucoside), the biomarker of Lonicera japonica, was efficiently bio-synthetized from its cheaper precursor luteolin. The structure of luteoloside was characterized by LC-MS and NMR analyses. Compared to the significant inhibitory effect of luteolin on human hepatocyte cell line LO2 at high doses, luteoloside did not show obvious cytotoxic effects at any test dose. Moreover, luteoloside exhibited obvious promotive effects on human hepatocyte cells, suggesting a potential application in hepatoprotective therapies.


The anti-inflammatory NHE-06 restores antitumor immunity by targeting NF-κB/IL-6/STAT3 signaling in hepatocellular carcinoma.[Pubmed: 29574282]


The NF-κB/IL-6/STAT3 inflammatory axis is highly activated in a variety of inflammation-related cancers and contributes to suppression of antitumor immunity. In this study, we generated a novel herbal formula NHE-06, a water-decocting extract from six natural herbals, Ficus carica, Taraxacum mongolicum, Angelica sinensis, Lonicera japonica, Pseudo-ginseng and Folium ginkgo. We investigated the anti-inflammatory properties of NHE-06 and its antitumor efficacy in hepatocellular carcinoma, a typical inflammation-related cancer. We found that NHE-06 effectively suppressed NF-κB/IL-6/STAT3 signaling and enhanced antitumor immunity both in vitro and in HCC-bearing mice. In a subcutaneous HCC mouse model, we found that NHE-06 possessed both preventive and therapeutic functions. Moreover, rather than the cytotoxic effects, the antitumor efficacy of NHE-06 was indispensable of intact immunity, since the therapeutic effect was only achieved in immunocompetent mice whereas failed in immunocompromised mice. Taken together, the novel formula of the anti-inflammatory NHE-06 effectively restores antitumor immunosurveillance and can be applied for prevention and/or treatment of inflammation-related cancers.