Natural Products from Morinda officinalis

Natural Products Isolated from Morinda officinalis

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 Morinda officinalis
Natural products isolated from Morinda officinalis

Natural Products from Morinda officinalis

14 natural product s associated with Morinda officinalis

Natural products and bioactive compounds from Morinda officinalis
Catalog No. Product Name CAS Number COA
BCN3478 1-Hydroxy-2-methylanthraquinone
1-Hydroxy-2-methylanthraquinone chemical structure
6268-09-3 COA
BCN8292 1-Kestose
1-Kestose chemical structure
470-69-9 COA
BCN3091 2-Hydroxy-1-methoxyanthraquinone
2-Hydroxy-1-methoxyanthraquinone chemical structure
6170-06-5 COA
BCN6231 Asperuloside
Asperuloside chemical structure
14259-45-1 COA
BCN3088 Asperulosidic acid
Asperulosidic acid chemical structure
25368-11-0 COA
BCN3323 Deacetylasperulosidic acid
Deacetylasperulosidic acid chemical structure
14259-55-3 COA
BCN5989 Fumaric acid
Fumaric acid chemical structure
110-17-8 COA
BCN2327 Isofraxidin
Isofraxidin chemical structure
486-21-5 COA
BCN6280 Monotropein
Monotropein chemical structure
5945-50-6 COA
BCN5397 Nystose
Nystose chemical structure
13133-07-8 COA
BCN5663 Physcion
Physcion chemical structure
521-61-9 COA
BCN6047 Rubiadin
Rubiadin chemical structure
117-02-2 COA
BCN4298 Rubiadin 1-methyl ether
Rubiadin 1-methyl ether chemical structure
7460-43-7 COA
BCN5890 Succinic acid
Succinic acid chemical structure
110-15-6 COA

References

[Rapidly identify oligosaccharides in Morinda officinalis by UPLC-Q-TOF-MSE].[Pubmed: 29676129]


In this paper, an approach was applied for separation and identification of oligosaccharides in Morinda officinalis How by Ultra performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) with collision energy. The separation was carried out on an ACQUITY UPLC BEH Amide C₁₈(2.1mm×100 mm，1.7 μm) with gradient elution using acetonitrile(A) and water(B) containing 0.1% ammonia as mobile phase at a flow rate of 0.2 mL·min⁻¹. The column temperature was maintained at 40 °C. The information of accurate mass and characteristic fragment ion were acquired by MSE in ESI negative mode in low and high collision energy. The chemical structures and formula of oligosaccharides were obtained and identified by the software of UNIFI and Masslynx 4.1 based on the accurate mass, fragment ions, neutral losses, mass error, reference substance, isotope information, the intensity of fragments, and retention time. A total of 19 inulin oligosaccharide structures were identified including D(+)-sucrose, 1-kestose, nystose, 1F-fructofuranosyl nystose and other inulin oligosaccharides (DP 5-18). This research provided important information about the inulin oligosaccharides in M. officinalis. The results would provide scientific basis for innovative utilization of M. officinalis.


Protective effect of MOTILIPERM in varicocele-induced oxidative injury in rat testis by activating phosphorylated inositol requiring kinase 1α (p-IRE1α) and phosphorylated c-Jun N-terminal kinase (p-JNK) pathways.[Pubmed: 29316840]


MOTILIPERM was prepared as a mixture of extracts of three medicinal herbs [roots of Morinda officinalis How (Rubiaceae), outer scales of Allium cepa L. (Liliaceae) and seeds of Cuscuta chinensis Lamark (Convolvulaceae)].


Bioassay-Guided Isolated Compounds from Morinda officinalis Inhibit Alzheimer's Disease Pathologies.[Pubmed: 28961196]


None