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Ligustrum lucidum

Ligustrum lucidum

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Natural products/compounds from  Ligustrum lucidum

  1. Cat.No. Product Name CAS Number COA
  2. BCN5966 Salidroside10338-51-9 Instructions
  3. BCN5871 2-(3,4-Dihydroxyphenyl)ethanol10597-60-1 Instructions
  4. BCN2370 Ligustroflavone260413-62-5 Instructions
  5. BCN5246 Oleuropein32619-42-4 Instructions
  6. BCN5444 Nuezhenide39011-92-2 Instructions
  7. BCN5524 Betulinic acid472-15-1 Instructions
  8. BCN5528 Betulin473-98-3 Instructions
  9. BCN5600 Luteolin491-70-3 Instructions
  10. BCN6307 Arbutin497-76-7 Instructions
  11. BCN5608 2-(4-Hydroxyphenyl)ethanol501-94-0 Instructions
  12. BCN5616 Oleanolic acid508-02-1 Instructions
  13. BCN5388 Luteolin-7-O-glucoside5373-11-5 Instructions
  14. BCN5725 Lupeol545-47-1 Instructions
  15. BCN1206 Palmitic acid57-10-3 Instructions
  16. BCN5788 Cosmosiin578-74-5 Instructions
  17. BCN4136 Acteoside61276-17-3 Instructions
  18. BCN4154 4-Hydroxybenzyl alcohol623-05-2 Instructions
  19. BCN9061 (±)-Naringenin67604-48-2 Instructions
  20. BCN4327 Ursolic acid77-52-1 Instructions
  21. BCN7818 Chicanine78919-28-5 Instructions
  22. BCN4953 Echinacoside82854-37-3 Instructions

References

Molecular modeling of non-covalent binding of Ligustrum lucidum secoiridoid glucosides to AP-1/matrix metalloproteinase pathway components.[Pubmed: 29687366]


Ligustrum lucidum secoiridoid glucosides have been demonstrated to treat various types of diseases such as inflammation, pain, hepatotoxicity and hyperlipidermic as well as tonic for liver and kidney. Matrix metalloproteinases (MMPs) play a key role upon the pathology of photoaging. The present computational study showed that among the six secoiridoid glucosides (ligustroside, lucidumoside A, lucidumoside C, neonuezhenide, oleoside dimethylester, and oleuropein), ligustroside and lucidumoside A competitively inhibit all MMP-1, MMP-3, and MMP-9 activities in the docking models. The molecular docking analysis revealed a network of interactions between MMP-1, MMP-3, and MMP-9 and the ligands; ligustroside and lucidumoside A, and oxygen-containing and hydrophobic functional groups appear to be responsible for these enhanced interactions. The effect of ligustroside and lucidumoside A on the transcription factor AP-1 action was also investigated using molecular docking and dynamics simulations. The experiments suggested that inhibition of an AP-1-DNA complex formation could be on account of the direct interference of AP-1 binding onto the DNA binding sequence by ligustroside and lucidumoside A. The results suggest that both compounds have the highest potential for application as an anti-aging agent with the MMP inhibitory and anti-transcriptional activities.


Leaf physiological and anatomical responses of Lantana and Ligustrum species under different water availability.[Pubmed: 29665510]


Understanding the plant characteristics that support tolerance to water stress is important in choosing plants in arid or semi-arid environments, such as the Mediterranean. In particular, leaf characteristics can affect the response of plants to water stress. In order to understand how plants with different leaf features can overcome water stress, four water regimes were adopted on two species that are widespread in the Mediterranean environment, Lantana camara and Ligustrum lucidum. The four treatments were: control (C), in which the pot substrate moisture was maintained close to water container capacity (WCC), light deficit irrigation (LDI) irrigated at 75% of WCC, moderate deficit irrigation (MDI) at 50% of WCC, and severe deficit irrigation (SDI) at 25% of WCC. To better understand the action mechanisms, the trial was repeated twice (from January to May, and from May to September). Morphological, anatomical and physiological data were measured to identify the action mechanisms. Water deficit significantly decreased the biomass accumulation in both species during the experimental growth period. In Lantana, significant variations in total leaf area and leaf number were registered between C and SDI, while in Ligustrum, the differences were significant only for total leaf area. The water deficit treatments reduced the leaf thickness especially in Ligustrum. In both species, photosynthesis reduction was related to stomatal closure. Ligustrum showed a higher variability among treatments indicating a faster and more efficient response to water limitations compared to Lantana, as also demonstrated by the lower biomass reduction in the most severe water stress treatment.


Secoiridoid analogues from the fruits of Ligustrum lucidum and their inhibitory activities against influenza A virus.[Pubmed: 29625823]


None


New secoiridoids from the fruits of Ligustrum lucidum.[Pubmed: 29589484]


Three new secoiridoids, nuezhenelenoliciside (1), isojaslanceoside B (2), 6'-O-trans-cinnamoyl-secologanoside (3), were isolated from the dried fruits of Ligustrum lucidum. Their structures were elucidated by comprehensive spectroscopic analysis. Among them, 1 featured a rare rearrangement product of secoiridoid, which underwent the cleavage of chemical bond between C-1 and O-2, and the reformation of a new iridoid ring between C-8 and O-2. In addition, all compounds were tested for their osteogenic activity on pre-osteoblastic MC3T3-E1 cells. As a result, 1 and 3 exhibited potent effects on promoting cell proliferation of pre-osteoblast cells.


Screening and isolation of potential neuraminidase inhibitors from leaves of Ligustrum lucidum Ait. based on ultrafiltration, LC/MS, and online extraction-separation methods.[Pubmed: 29525364]


Ultrafiltration liquid chromatography-mass spectrometry (ultrafiltration LC/MS) is introduced as an efficient method that can be applied to rapidly screen and identify ligands from the leaves of Ligustrum lucidum Ait. Using this method, we identified 13 compounds, including organic acids, flavonoids, and glycosides, as potent neuraminidase inhibitors. A continuous online method, employing pressurized liquid extraction followed by parallel centrifugal partition chromatography and preparative liquid chromatography PLE-(parallel-CPC/PLC), was developed for the efficient, scaled-up production of 12 compounds with high purities. The bioactivities of the separated compounds were assessed by an in vitro enzyme inhibition assay. The use of ultrafiltration LC/MS combined with PLE-(parallel-CPC/PLC), and an in vitro enzyme inhibition assay facilitated the efficient screening and isolation of neuraminidase inhibitors from complex samples, and could serve as an important platform for the large-scale production of functional ingredients.