Richenoic acid
Reference standards.
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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.
RSC Advances2017, 86
Biomed Pharmacother.2022, 156:113929.
J Agric Food Chem.2023, 71(47):18510-18523.
Korean J. Food Preserv. 2021, 28(6):846-856.
Separations2021, 8(1), 1.
Pharmacognosy Journal2019, 11(2): 369-373
Microchemical Journal2022, 182: 107874.
Fitoterapia.2022, 105141.
J of Applied Biological Chem.2020, 63(2):147-152
J Agric Food Chem.2020, 68(43):12164-12172.
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Phytochemistry. 2001 May;57(1):131-4.
ent-Pimarane derivatives from Dysoxylum hainanense.[Pubmed:
11336254]
METHODS AND RESULTS:
Four ent-pimarene diterpenoids. ent-18-acetoxy-8(14)-pimarene-15S, 16-diol, ent-18-acetoxy-16-hydroxy-8(14)-pimaren-15-one, ent-16,18-dihydroxy-8(14)-pimaren-15-one and ent-19-nor-4,16,18-trihydroxy-8(14)-pimaren-15-one, together with three known damarane triterpenoids, Richenoic acid, eichleriainic acid and shoreic acid were isolated from the bark of Dysoxyhum hainanense Merr. Their structures were elucidated on the basis of spectroscopic techniques.
CONCLUSIONS:
The absolute configurations of four diterpenoids were assigned as ent-pimarene type by chemical transformation and by co-occurrence in the plant as well as by negative optical rotations for four compounds.
