Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide

Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide
Product Name Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide
CAS No.: 866602-52-0
Catalog No.: CFN70461
Molecular Formula: C32H50N2O2
Molecular Weight: 494.8 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Echinacea purpurea
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide exhibits potent anti-oxidant property.
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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.
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    Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide

    Catalog No: CFN70461
    CAS No: 866602-52-0
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    Planta Medica, 2011, 77(16):1794-1799.
    Absolute/relative bioavailability and metabolism of dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides (tetraenes) after intravenous and oral single doses to rats.[Reference: WebLink]
    The present study assessed the absolute and relative bioavailabilities of Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide (tetraenes), the main bioactive constituents in Echinacea, administered as pure compounds or in the form of an Echinacea purpurea root extract preparation.
    METHODS AND RESULTS:
    Tetraenes were administered orally by gavage or intravenously in a dose of 0.75 mg/kg. The extract was administered orally in a dose of 158.6 mg/kg which corresponds to the same amount of tetraenes. Pharmacokinetic parameters of tetraenes were calculated by non-compartmental analysis using WinNonlin® 5.2 software. Mean dodeca-2 E,4 E,8 Z,10 E/ Z-tetraenoic acid isobutylamide dose-normalized plasma area under the concentration-time curve (AUC₀-∞/dose) was 3.24 ± 0.32 min · ng/mL/µg and 0.95 ± 0.16 min · ng/mL/µg after iv and oral administrations, respectively, and 1.53 ± 0.18 min · ng/mL/µg after oral administration of the Echinacea root extract. The absolute oral bioavailability of dodeca-2 E,4 E,8 Z,10 E/ Z-tetraenoic acid isobutylamides was 29.2 ± 2.3 %, which was increased to 47.1 ± 7.2 % (1.6-fold) by administration of the Echinacea extract.
    CONCLUSIONS:
    Administration of an Echinacea extract increased blood exposure with no impact on C(max), but prolonged the elimination half-life to 123.3 ± 15.7 min in comparison to 35.8 ± 6.5 min after administration of the pure dodeca-2 E,4 E,8 Z,10 E/ Z-tetraenoic acid isobutylamides.
    Plant Cell Reports, 1991, 10(2):85-89.
    Agrobacterium rhizogenes-mediated transformation ofEchinacea purpurea.[Reference: WebLink]

    METHODS AND RESULTS:
    Echinacea purpurea seedlings were inoculated with several Agrobacterium rhizogenes strains in order to obtain hairy roots. Infection with A. rhizogenes strains LMG63 and LMG150 resulted in callus formation. Upon infection with strains ATCC 15834 and R1601 hairy roots were obtained. Opine detection confirmed transformation of E. purpurea.
    CONCLUSIONS:
    Comparative HPLC fingerprint analysis of the alkamides from natural plant source, control tissues, and transformed callus and roots indicated that transformed callus and hairy roots might be a promising source for continuous and standardized production of theDodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide and related amides.
    American journal of plant sciences, 2015, 6(12):201-212.
    Effect of Extraction Methods on the Active Compounds and Antioxidant Properties of Ethanolic Extracts of Echinacea purpurea Flower.[Reference: WebLink]

    METHODS AND RESULTS:
    The extraction yields, active compounds and antioxidant properties of 50%-aqueous-ethanolic extracts of freeze-dried Echinacea purpurea flower with multi-steps and multi-batches extraction methods were assessed. In multi-steps extraction, the extraction yields of 1st, 2nd, and 3rd extracts were 21.52%, 9.33%, and 2.90%, and their total phenols contents were 182.08, 176.33, and 177.08 mg CAE/g, respectively, with cichoric acid (62.07-66.57 mg/g) being the main phenolic compound. No differences in the contents of individual and total caffeic acids derivates existed among 1st, 2nd, and 3rd extracts. The Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide(alkamide 8/9) contents of 1st, 2nd, and 3rd extracts were 505.38, 598.61, and 585.99 µg/g, respectively. In multi-batches extraction, the extracted dry weight increased with increasing the sample batches, with the extraction yields and alkamide 8/9 contents of samples decreased from 19.93% to 12.98% and 534.36 to 269.76 µg/g, respectively.
    CONCLUSIONS:
    The total phenol (177.25-186.92 mg CAE/g), individual and total caffeic acid derivatives (85.99-95.06 mg/g) contents of extracts among different sample batches were not significantly different, with cichoric acid (63.66-70.31 mg/g) being the main phenolic compound. All the prepared extracts also exhibited potent anti-oxidant properties. Overall, the two-step sequential extraction is desirable for extracting bioactive compounds from freeze-dried E. purpurea flower.
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