Streptenol E

Streptenol E
Product Name Streptenol E
CAS No.: N/A
Catalog No.: CFN00042
Molecular Formula: C12H21NO3
Molecular Weight: 227.30 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Oil
Source: From Streptomyces sp.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Reference standards.
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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.
  • Int J Mol Sci.2022, 23(21):13112.
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  • Food Funct.2021, 12(13):5892-5902.
  • Phytother Res.2016, 30(12):2020-2026
  • Molecules.2018, 23(9):E2121
  • Chinese Pharmacological Bulletin2019, 35(8):1120-1125
  • Regul Toxicol Pharmacol.2024, 149:105620.
  • Heinrich Heine University Dusseldorf2021, 62203.
  • Antioxidants (Basel).2022, 11(12):2327.
  • Food Funct.2022, 13(14):7638-7649.
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    J Nat Prod. 2001 Jan;64(1):42-5.
    New co-metabolites of the streptazolin pathway.[Pubmed: 11170664]

    METHODS AND RESULTS:
    Variation of the culture conditions of Streptomyces sp. strain A1, which produces streptazolin (1), resulted in the isolation of four new co-metabolites: 5-O-(beta-D-xylopyranosyl)streptazolin (3), 9-hydroxystreptazolin (4), 13-hydroxystreptazolin (5), and Streptenol E (6). Their structures were established by spectroscopic and chemical methods. The possible biosynthetic relationship between the streptazolins and the streptenols is discussed.
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