USBio Logo

045136 Pellitorine CAS: 18836-52-7

Specifications
References
CAS Number
18836-52-7
Grade
Highly Purified
Molecular Formula
C14H25NO
Molecular Weight
223.4
EU Commodity Code
38220090
Shipping Temp
RT
Storage Temp
-20°C
(E,E)-N-(2-Methylpropyl) 2,4-decadienamide, BRN 1725967

Cell-permeable. A natural product isolated from the roots of Piper Nigrum. Shows larvicidal, antimycobacterial and antituberculosis activity. Modulator of the sensory neuron function to induce tingling parethesia. Tingling-inducing agent. Excellent stable model compound for sensory studies. alpha-Glucosidase inhibitor used in diabetes mellitus, cancer, infection and inflammatory research. ACAT (Acyl-CoA cholesteryl acyl transferase) inhibitor. Potential anti-cancer lead compound.

Source
Synthetic. Originally isolated from roots of Anacyclus pryrethrum and fruits of Piper nigrum.
Synonyms
(2E,4E)-N-(2-Methylpropyl)-2,4-decadienamide; BRN 1725967
CAS Number
18836-52-7
Molecular Formula
C14H25NO
Molecular Weight
223.4
Appearance
Supplied as a yellow to beige solid.
Purity
≥97% (HPLC)
Solubility
100% ethanol, methanol, DMSO or dichloromethane. Sparingly soluble in water.
Storage and Stability
Store at -20°C. Caution: Light-sensitive. For maximum recovery of product, centrifuge the original vial prior to removing the cap.
Source
Synthetic
Purity
≥97% (HPLC)
Form
Supplied as a yellow to beige solid.
Important Note
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
References
1. Larvicidal activity of isobutylamides identified in Piper nigrum fruits against three mosquito species: I.K. Park, et al.; J. Agric. Food Chem. 50, 1866 (2002)|2. Chemical constituents and bioactivity of Piper sarmentosum: T. Rukachaisirikul, et al.; J. Ethnopharmacol. 93, 173 (2004)|3. Stereoselective Enzymatic Synthesis of cis-Pellitorine, a Taste Active Alkamide Naturally Occurring in Tarragon: P. J. Ley, et al.; Eur. J. Org. Chem. 2004, 5135 |4. Chemical constituents of the roots of Piper sarmentosum: P. Tuntiwachwuttikul, et al.; Chem. Pharm. Bull. (Tokyo) 54, 149 (2006)|5. HPLC assisted chemobiological standardization of alpha-glucosidase-I enzyme inhibitory constituents from Piper longum Linn - An Indian medicinal plant: S.V. Pullela, et al.; J. Ethnopharmacol. 108, 445 (2006)|6. ACAT inhibition of alkamides identified in the fruits of Piper nigrum: M.C. Rho, et al.; Phytochemistry 68, 899 (2007)|7. Pellitorine, a potential anti-cancer lead compound against HL6 and MCT-7 cell lines and microbial transformation of piperine from Piper Nigrum: G.C. Ee, et al.; Molecules 15, 2398 (2010)
USBio References
No references available
Pricing
Order
Proceed to Checkout
Cart Summary
ProductSizeListYour PriceQtyExt Price
Subtotal:Subtotal:
Subtotal:Subtotal:
Total Coupon Savings:Total Coupon Savings:()
Your cart is currently empty.
- Coupon Code
Recently Viewed
  • Contact Us

    Visit our technical library or contact our support staff to answer your questions.

    Telephone:
    1-800-520-3011

    Library | Contact

    Distributors

    For customers outside of the United States, please use one of our many distributors.

    View Distributors

    Payment Methods

    We accept the following payment methods as well as pay-by-invoice.

    MasterCard Visa PayPal
    © 2023-2024 United States Biological - All Rights Reserved