ent-3-Oxokaurane-16,17-diol

ent-3-Oxokaurane-16,17-diol
Product Name ent-3-Oxokaurane-16,17-diol
CAS No.: 135683-73-7
Catalog No.: CFN99423
Molecular Formula: C20H32O3
Molecular Weight: 320.5 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Croton laevigatus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
AKaurane-3,16,17-triol,ent-kaurane-3-oxo-16α,17-diol,and ent-16α,17-dihydroxyatisan-3-one are three kinds of toxic diterpenoids isolated from the roots of genus Euphorbia.
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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.
  • Sci Rep.2017, 7(1):3249
  • Drug Des Devel Ther.2020, 14:969-976.
  • J Mol Med (Berl).2018, 96(7):661-672
  • Food Chem Toxicol.2020, 135:110863
  • Chin. Med.J.Res. Prac.2017, 31(4)
  • J Ethnopharmacol.2024, 318:116863.
  • ACS Nano.2018, 12(4):3385-3396
  • Int J Biol Macromol.2020, 169:342-351
  • Integr Med Res.2017, 6(4):395-403
  • HortTechnology2016, 26(6):816-819
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    Chinese Journal of Natural Medicines,2010,8(2):101-3.
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    To study the terpenes in the roots of Euphorbia fischeriana.
    METHODS AND RESULTS:
    The compounds were isolated by silica gel column chromatography,and their structures were identified on the basis of physiochemical and spectral data. Eight diterpenes and four triterpenes were obtained from the ethyl acetate extract,and their structures were elucidated as jolkinolide A(1),jolkinolide B(2),prostratin(3),ent-kaurane-3-oxo-16α,17-diol(ent-3-Oxokaurane-16,17-diol,4),antiquorin(5),neriifolene(6),ent-atisane-3β,16α,17-triol(7),kauranoic acid(8),aleuritolic acid(9),24-methyl-enecy- cloartanol(10)and lupenyl acetate(11).
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    Compounds 4-10 were isolated from this plant for the first time.
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