Buxbodine D

Buxbodine D
Product Name Buxbodine D
CAS No.: 390362-53-5
Catalog No.: CFN98627
Molecular Formula: C28H46N2O
Molecular Weight: 426.7 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Buxus bodinieri Levl.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Standard reference
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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 Pharm Biomed Anal.2024, 251:116444.
  • National University of Pharmacy2022, 1:73-76
  • J of Physics Conference Series2019, 1349(1)
  • Food Chem.2017, 221:1135-1144
  • Sci Rep.2019, 9:19059
  • Appl. Sci.2020, 10(20),7374.
  • Carbohydrate Polymer Technologies & App.2021, 2:100049.
  • Int. J. Mol. Sci.2022, 23(8), 4130.
  • Journal of Ginseng Research2021, 15 June.
  • Russian J. Bioorganic Chemistry2024, 50:2897-2903.
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    Acta Botanica Yunnanica, 2001,23(3):357-62.
    Steroidal Alkaloids from Buxus bodinieri[Reference: WebLink]
    Five new steroidal alkaloids have been isolated from Buxus bodinieri Lévl.,a common ornamental in South-China.
    METHODS AND RESULTS:
    On the basis of IR, UV, MS, NMR spectral analyses and chemical evidence, the chemical structure of these new steroidal alkaloids were deduced as: buxbodine A (1)(20α- dimethylamino-9β,19-cyclo-4,4,14α-trimethy-5α-pregnane); Buxbodine B (2)(16β-hydroxy-20α-dimethylamino-9β,19-cyclo-4,4,14α-trimethy-5α-pregn-1(2)-en-3-one); buxbodine C (3)(3β-dimethylamino-9β,19-cyclo-4,4,14α-trimethy-5α-pregn-6(7), 17 (20)-dien-16-one), Buxbodine D (4)(3β-dimethylamino-20α-acetoxylamino-9β,19-cyclo -4,4,14α-trimethy-5α-pregn-6(7)-ene) and buxbodine E (5)(3(-dimethylamino-20α-amino -9β,19-cyclo-4,4,14α-trimethy-5α-pregn-6(7)-ene), respectively.
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