A potent capsaicin/TRPV1 antagonist
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CAY10448

Item No. 10005633

Technical Information
Formal Name
N-[(4-hydroxy-2-iodo-3-methoxyphenyl)methyl]-8-methyl-nonanamide
CAS Number
1177195-52-6
Molecular Formula
C18H28INO3
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 30 mg/mlEthanol:PBS (pH 7.2)(1:2): .25 mg/ml
λmax
210, 236, 287 nm
SMILES
COc1cc(CNC(=O)CCCCCCC(C)C)c(I)cc1O
InChi Code
InChI=1S/C18H28INO3/c1-13(2)8-6-4-5-7-9-18(22)20-12-14-10-17(23-3)16(21)11-15(14)19/h10-11,13,21H,4-9,12H2,1-3H3,(H,20,22)
InChi Key
WPVUDCLXIKWQHK-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Capsaicin is the primary active component of the heat and pain-eliciting lipid soluble fraction of the Capsicum pepper.1 Capsaicin signals are transduced by a heat-activated ion channel, the vanilloid receptor 1 (VR1), or transient receptor potential vanilloid 1 (TRPV1).2 CAY10448 is an iodinated nonivamide, a potent capsaicin receptor antagonist with an IC50 value of approximately 10 nM.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Gannett, P.M., Nagel, D.L., Reilly, P.J., et alThe capsaicinoids: Their separation, synthesis, and mutagenicity. The Journal of Organic Chemistry 53(5), 1064-1071 (1988).

    2. Caterina, M.J., Schumacher, M.A., Tominaga, M., et alThe capsaicin receptor: A heat-activated ion channel in the pain pathway. Nature 389(6653), 816-824 (1997).

    3. Daddario, N., Minassi, A., Appendino, G., et alThe taming of capsaicin. Synthesis and vanilloid antagonistic activity of isosteric and regioisomeric halononiv amides and their products of halogen-carbon exchange. 14th Annual Symposium on the Cannabinoids 137-137 (2004).