Albatrelin A
Albatrelin A is a natural product from Albatrellus ovinus.
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.
Nutrients.2024, 16(16):2612.
ACS Chem Biol.2019, 14(5):873-881
Acta Biochim Pol.2015, 62(2):253-8
Evid Based Complement Alternat Med.2017, 2017:7383104
Mol Cells.2018, 41(8):771-780
Int Immunopharmacol.2024, 141:112906.
Nutrients.2018, 10(10)
Korean Herb. Med. Inf.2021, 9(2):231-239.
J of Food Quality2020, 8851285.
ACS Nano.2023, 17(11):9972-9986.
Related and Featured Products
J Nat Prod. 2013 Jan 25;76(1):79-84.
Meroterpenoid pigments from the basidiomycete Albatrellus ovinus.[Pubmed:
23305465]
METHODS AND RESULTS:
Eight grifolin derivatives, involving three new monomers, Albatrelin A, albatrelin B, albatrelin C (1-3), three novel dimers (meroterpenoid pigments), albatrelin D, albatrelin E, albatrelin F (4-6), and two known ones, 6a,7,8,9,10,10a-hexahydro-3,6,9-trimethyl-6-(4-methyl-3-penten-1-yl)-1,9-epoxy-6H-dibenzo[b,d]pyran (7) and confluentin (8), were isolated from Albatrellus ovinus. Their structures were established by extensive spectroscopic analysis. The absolute configurations of compounds 2-4 were determined as 9R by comparing their optical rotations with data reported in the literature.
CONCLUSIONS:
Albatrelin F (6) was isolated as a pair of C-2' tautomers with a ratio of 1.3:1. Confluentin (8) showed weak cytotoxicity against four human tumor cell lines, HL-60, SMMC-7712, A-549, and MCF-7, in vitro.
