Stigmasta-4,22,25-trien-3-one
Stigmasta-4,22,25-trien-3-one is a natural product from Callicarpa giraldiana.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Fitoterapia.2015, 100:179-86
Biomed Pharmacother.2019, 116:108987
Journal of Food Quality2022, P:13, 6256310.
Applied Biological Chemistry2023, 66:8
Int J Mol Sci.2022, 23(24):16000.
J of Food Quality2020, 8851285.
Naunyn Schmiedebergs Arch Pharmacol.2021, 394(1):107-115.
J Agric Food Chem.2020, 68(51):15164-15175
BMC Complement Altern Med.2014, 14:352
Molecules.2017, 22(12)
Related and Featured Products
Natural Product Communications , 2008 , 3 (11) :1787-1792.
Secondary metabolites from Clerodendrum chinense[Reference:
WebLink]
METHODS AND RESULTS:
Chemical studies carried out on Clerodendrum chinense yielded three new compounds including the steroid (22E, 24S)-Stigmasta-4,22,25-trien-3-one (1), the flavone glycoside 7, 8, 4′-trihydroxyflavone-6-O-β-D- glucuronopyranoside (2) and the epimeric neo-clerodane 14, 15-dihydro-15ξ- hydroxyclerodendrin A (3). Two acetylated derivatives of compound 3-, 2α-acetoxy-14, 15-dihydro-15ξ-hydroxyclerodendrin A (4) and 2α-acetoxy-14, 15-dihydro-15ξ-methoxyclerodendrin A (5) were also prepared, which have not been reported previously.
CONCLUSIONS:
The structure of each compound was elucidated by spectroscopic means.
