3beta-Hydroxylanosta-8,24-diene-21-al
3beta-Hydroxylanosta-8,24-diene-21-al may have cancer cell growth inhibitory activity against P388, HL-60, L1210 and KB cell lines.
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 Chem Inf Model.2021, 61(11):5708-5718.
Food Quality and Safety2018, 2:213-219
Environ Toxicol.2022, 37(3):514-526.
Applied Physics B2021, 127(92).
Food Chem.2019, 274:345-350
Free Radic Biol Med.2016, 97:307-319
Molecules.2018, 23(3):E615
J.Korean Soci. Food Sci. Nutri.2024, 53(11):1166-1177
ACS Omega.2023, 9(1):1278-1286.
Genes Genomics.2020, 10.1007
Related and Featured Products
Phytochemistry Letters, 2011 ,4 (3) :328-332.
New lanostane-type triterpenoids, inonotsutriols D, and E, from Inonotus obliquus[Reference:
WebLink]
Two new lanostane-type triterpenoids, inonotsutriols D ( 1) and E ( 2), were isolated from the sclerotia of Inonotus obliquus (Pers.: Fr.) Pil. (Japanese name: kabanoanatake; Russian name: chaga).
METHODS AND RESULTS:
Their structures were determined to be lanost-8-ene-3β,22 R,24 R-triol ( 1) and lanost-8-ene-3β,22 R,24 S-triol ( 2) on the basis of spectral data, including 2D NMR analysis. In addition, major compounds, inotodiol ( 3), trametenolic acid ( 4), 3beta-Hydroxylanosta-8,24-diene-21-al( 5), 21-hydroxylanosterol ( 6), inonotsuoxide A ( 7) and inonotsuoxide B ( 8) were identified, and all compounds, except 2, were evaluated for their cancer cell growth inhibitory activity against P388, HL-60, L1210 and KB cell lines.
