Bi-linderone
Bi-linderone shows significant activity against glucosamine-induced insulin resistance in HepG2 cells at a concentration of 1 microg/mL.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Sci Rep.2019, 9:12132
J Appl Microbiol.2022, 132(2):949-963.
Indian J. of Experimental Bio.2020, 9(58).
Separations2021, 8(1), 1.
Phytomedicine.2023, 117:154929.
Korean J. Food Sci. & Technol.2022, 54(2):241-246
Key Engineering Materials2022, 931(47-53).
Journal of Medicinal Food2023, Vol.26(10).
Pharmaceuticals.2022, 15(4), 402.
Evidence-based Compl.&Alternative Med.2023, 5417813
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Org Lett. 2010 May 21;12(10):2354-7.
Bi-linderone, a highly modified methyl-linderone dimer from Lindera aggregata with activity toward improvement of insulin sensitivity in vitro.[Pubmed:
20420414]
METHODS AND RESULTS:
Bi-linderone (1) was isolated as racemate from the traditional Chinese medicinal plant Lindera aggregata. The structure elucidation of Bi-linderone was reported on the basis of extensive analysis of NMR spectra and crystal X-ray diffraction.
CONCLUSIONS:
Bi-linderone has an unprecedented spirocyclopentenedione-containing carbon skeleton and showed significant activity against glucosamine-induced insulin resistance in HepG2 cells at a concentration of 1 microg/mL.
Org Lett. 2011 May 6;13(9):2192-5.
Biomimetic total syntheses of linderaspirone A and bi-linderone and revisions of their biosynthetic pathways.[Pubmed:
21446662]
METHODS AND RESULTS:
Simple exposure to sunlight is sufficient for triggering photochemical [2 + 2] cycloaddition-Cope or radical rearrangement cascades in the naturally occurring methyl linderone, leading to efficient biomimetic total syntheses of linderaspirone A and Bi-linderone, two recently discovered bioactive spirocyclopentenedione natural products.
