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    Lathyranoic acid A
    Lathyranoic acid A
    Information
    CAS No. 850560-44-0 Price $318 / 5mg
    Catalog No.CFN95325Purity>=98%
    Molecular Weight494.6Type of CompoundDiterpenoids
    FormulaC29H34O7Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)  (SDF)
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / $318 / In-stock
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    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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  • Lathyranoic acid A Description
    Source: The herbs of Stellera chamaejasme
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: 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

    After receiving: 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.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.0218 mL 10.1092 mL 20.2184 mL 40.4367 mL 50.5459 mL
    5 mM 0.4044 mL 2.0218 mL 4.0437 mL 8.0873 mL 10.1092 mL
    10 mM 0.2022 mL 1.0109 mL 2.0218 mL 4.0437 mL 5.0546 mL
    50 mM 0.0404 mL 0.2022 mL 0.4044 mL 0.8087 mL 1.0109 mL
    100 mM 0.0202 mL 0.1011 mL 0.2022 mL 0.4044 mL 0.5055 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    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.
    Lathyranoic acid A: first secolathyrane diterpenoid in nature from Euphorbia lathyris[Pubmed: 15787511]
    Lathyranoic acid A (1), the first secolathyrane diterpenoid with an unprecedented skeleton, and a new diterpenoid Euphorbia factor L11 (2) were isolated from the seeds of Euphorbia lathyris. Their structures were elucidated by spectroscopic analysis and chemical methods. A biogenetic route involving an enzymatic Baeyer-Villiger oxidation as the key step was postulated for the transformation of 2 to 1 and mimicked by an unusual chemical Baeyer-Villiger oxidation.
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