Chartarlactam A
Chartarlactam A shows antihyperlipidemic effects in HepG2 cells.
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.
J Anal Toxicol.2021, bkab015.
Phytother Res.2018, 32(5):923-932
Journal of Apiculture2023.38(3):249-254.
Sci Rep. 2018, 462(8)
Front Cell Dev Biol.2021, 9:764263.
Plant Biotechnol (Tokyo).2024, 41(3):267-276.
Lab Chip.2018, 18(6):971-978
Int J Mol Sci.2022, 23(20):12516.
Appl. Sci.2022, 12(17), 8646.
Appl. Sci. 2024, 14(13), 5815
Related and Featured Products
J Nat Prod. 2014 Jan 24;77(1):138-47.
Chartarlactams A-P, phenylspirodrimanes from the sponge-associated fungus Stachybotrys chartarum with antihyperlipidemic activities.[Pubmed:
24387683 ]
Chemical examination of the solid culture of the endophytic fungus Stachybotrys chartarum isolated from the sponge Niphates recondita resulted in the isolation of 16 new phenylspirodrimanes, named chartarlactams A-P (1-16), together with eight known analogues.
METHODS AND RESULTS:
Their structures were determined on the basis of extensive spectroscopic analysis, including X-ray single-crystal diffraction for the determination of the absolute configurations. The isoindolone-drimane dimer chartarlactam L (12) was determined as a new skeleton.Compounds 1-6(Chartarlactam A,chartarlactam B, chartarlactam C, chartarlactam D, chartarlactam E, chartarlactam F ) and 8-24 were evaluated for antihyperlipidemic effects in HepG2 cells, and the primary structure-activity relationships are discussed.
