Randialic acid B
Randialic acid B shows significant cell-protective effects against H2O2-induced H9c2 cardiomyocyte injury.
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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.
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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.
J. of Agricultural Science2015, 1916-9760
Korean Journal of Pharmacognosy2017, 48(4):320-328
Agronomy 2021, 11(3),502.
Molecules.2021, 26(19):6032.
Process Biochemistry2019, 85:106-115
FEBS Lett.2021, 595(20):2608-2615.
Antioxidants (Basel).2019, 8(8):E307
Fitoterapia.2024, 106006.
Chin Med.2022, 17(1):66.
J Chem Inf Model.2021, 61(11):5708-5718.
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Chin J Nat Med. 2017 Feb;15(2):115-120.
Three new triterpenoids isolated from the aerial parts of Ilex cornuta and protective effects against H2O2-induced myocardial cell injury.[Pubmed:
28284425 ]
METHODS AND RESULTS:
In the present study, three new triterpenoids, 23-hydroxyurs-12, 18-dien-28-oic acid 3β-O-α-L-arabinopyranoside (1), 23-hydroxyurs-12, 18-dien-28-oic acid 3β-O-β-D-glucuronopyranoside-6-O-methyl ester (2), and urs-12, 18-dien-28-oic acid 3β-O-β-D-glucuronopyranoside-6-O-methyl ester (3), and a known triterpenoid, 3β-hydroxy-urs-2, 18-dien-28-oic acid (4, Randialic acid B), were isolated from the aerial parts of Ilex cornuta. Their structures were identified by the spectroscopic analyses (IR, ESI-MS, HR-ESI-MS, and 1D and 2D NMR) and chemical reactions.
CONCLUSIONS:
Compound 4 showed significant cell-protective effects against H2O2-induced H9c2 cardiomyocyte injury. Compounds 1-4 did not show any significant DPPH radical scavenging activity.
