Lathyranoic acid A

Lathyranoic acid A
Product Name Lathyranoic acid A
CAS No.: 850560-44-0
Catalog No.: CFN95325
Molecular Formula: C29H34O7
Molecular Weight: 494.6 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Stellera chamaejasme
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $318/5mg
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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.
  • Chem. of Vegetable Raw Materials2020, 97-105
  • J Food Sci Technol.2019, 56(5):2712-2720
  • Biorxiv.2020, doi: 10.1101.
  • Biochem Biophys Res Commun.2019, 518(4):732-738
  • Evid Based Complement Alternat Med.2020, 2020:1970349.
  • International J of Green Pharmacy2019, 13(3)
  • Clin Transl Oncol.2019, 10.1007
  • Applied Biological Chemistry2020, 63:33(2020)
  • The Journal of Phytopharmacology2020, 9(1): 1-4
  • Pharmaceutical Chemistry Journal2019, 52(12):986-991
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    J Org Chem . 2011 Mar 4;76(5):1448-51.
    Total synthesis of lathyranoic acid A[Pubmed: 21275399]
    The first total synthesis of Lathyranoic acid A (1) was accomplished stereoselectively in a linear sequence of 20 steps and an overall yield of 1.4%. This modular synthesis featured a cyclic, stereocontrolled Cu-catalyzed intramolecular cyclopropanation to construct the cis-cyclopropane unit, a Grubbs metathesis to construct the γ-substituted cyclopentenone moiety, and an anion-mediated conjugate addition.
    Org Lett . 2005 Mar 31;7(7):1379-82.
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