N-Acetyl-5,6-dehydrololine

N-Acetyl-5,6-dehydrololine
Product Name N-Acetyl-5,6-dehydrololine
CAS No.: 194205-01-1
Catalog No.: CFN00295
Molecular Formula: C10H14N2O2
Molecular Weight: 194.23 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Festuca argentina.
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.
  • Food Science and Biotechnology2022, 10.1007.
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  • Front Immunol.2018, 9:2091
  • bioRxiv - Biochemistry2023, 548213.
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    CAS No: 194205-01-1
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    J. Ethnopharmacol., 1997, 57(1):1-9.
    Alkaloids from endophyte-infected Festuca argentina.[Pubmed: 9234159]

    METHODS AND RESULTS:
    Five loline-type alkaloids, the known lolinine, N-formylloline, loline, N-methylloline and the new 5,6-dehydro-N-acetylloline(N-Acetyl-5,6-dehydrololine), were characterized from the pooid-grass endophyte-infected Festuca argentina . These compounds are not responsible for the toxicity of the plant, as shown upon i.p. injection into mice. Their probable phytoalexine role and chemotaxonomical significance are discussed.
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