3beta-Hydroxylanosta-8,24-diene-21-al

3beta-Hydroxylanosta-8,24-diene-21-al
Product Name 3beta-Hydroxylanosta-8,24-diene-21-al
CAS No.: 96574-03-7
Catalog No.: CFN92365
Molecular Formula: C30H48O2
Molecular Weight: 440.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The sclerotium of Poria cocos(Schw.)Wolf
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $318/5mg
3beta-Hydroxylanosta-8,24-diene-21-al may have cancer cell growth inhibitory activity against P388, HL-60, L1210 and KB cell lines.
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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.

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 Plant Biochem.Biotech.2024, 33:353-366.
  • Ethnomedicinal Plants for Drug Discovery2024, 491-509
  • Vietnam Journal of Food Control2022, 5(3):pp.390-401.
  • Evid Based Complement Alternat Med.2021, 2021:5319584.
  • Preprints2024, 2085.v1
  • J Neuroinflammation.2020, 17(1):75.
  • Antioxidants (Basel).2021, 10(3):379.
  • Molecules.2018, 23(10):E2638
  • Evid Based Complement Alternat Med.2020, 2020:2584783.
  • Processes2021, 9(11),2065.
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    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).
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    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.
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