7-O-Acetylbonducellpin C
7-O-Acetylbonducellpin C may exhibit significant inhibition of nitric oxide production of RAW264.7 macrophages stimulated by lipopolysaccharide (LPS).
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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.
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Nutrients.2024, 16(7):965.
Molecules.2023, 28(8):3414.
Pathogens.2018, 7(3):E62
Int J Mol Sci.2021, 22(16):8604.
Preprints2022, 202211.0388.v1.
Int J Mol Sci.2021, 22(21):11447.
Processes2022, 10(10), 2008.
Phytother Res.2020, 34(4):788-795.
J Med Food.2019, 22(10):1067-1077
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Phytochemistry. 2015 Sep;117:325-31
Anti-inflammation furanoditerpenoids from Caesalpinia minax Hance.[Pubmed:
26125942]
Cassane skeletons are rare in nature, but often possess valuable medicinal properties.
METHODS AND RESULTS:
A furanoditerpenoid with an unusual A-seco-rearranged cassane skeleton, neocaesalminin A, and five furanoditerpenoids were isolated from seeds of Caesalpinia minax Hance, along with six known cassane derivatives, 7-O-Acetylbonducellpin C, caesalmin F, caesalmin C, ΞΆ-caesalmin, caesalmin E1 and caesalpinin K. Compound structures were determined by spectroscopy (HR-ESI-MS, UV, IR, 1D NMR, 2D NMR), X-ray crystallography and quantum chemical computation of electronic circular dichroism).
CONCLUSIONS:
Three of the previously known compounds exhibited significant inhibition of nitric oxide production of RAW264.7 macrophages stimulated by lipopolysaccharide (LPS).
