Nordihydrocapsiate
| Code | Size | Price |
|---|
| CDX-N0121-M025 | 25 mg | £108.00 |
Quantity:
| CDX-N0121-M100 | 100 mg | £304.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
NDCT; (4-Hydroxy-3-methoxyphenyl)methyl 7-methyloctanoate; 4-Hydroxy-3-methoxybenzyl 7-methyloctanoate
Appearance:
Light yellow to brown liquid.
CAS:
220012-53-3
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H413
InChi:
InChI=1S/C17H26O4/c1-13(2)7-5-4-6-8-17(19)21-12-14-9-10-15(18)16(11-14)20-3/h9-11,13,18H,4-8,12H2,1-3H3
InChiKey:
BXBVPYSHEOQGHP-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 220012-53-3. Formula: C17H26O4. MW: 294.39. Synthetic Major capsaicinoid. TRPV1 and hTRPA1 agonist. Shown to activate capsaicin receptor, also called transient receptor potential vanilloid subfamily member 1 (TRPV1), but without inducing a nociceptive response. Anti-inflammatory and anticancer compound.
MDL:
MFCD28137841
Molecular Formula:
C17H26O4
Molecular Weight:
294.39
Package Type:
Vial
Precautions:
P273
Product Description:
Major capsaicinoid. TRPV1 and hTRPA1 agonist. Shown to activate capsaicin receptor, also called transient receptor potential vanilloid subfamily member 1 (TRPV1), but without inducing a nociceptive response. Anti-inflammatory and anticancer compound.
Purity:
>95% (HPLC)
SMILES:
COC1=CC(COC(=O)CCCCCC(C)C)=CC=C1O
Solubility Chemicals:
Soluble in methanol.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) K. Kobata, et al.; J. Nat. Prod. 62, 335 (1999) | (2) R. Sancho, et al.; Eur. J. Immunol. 32, 1753 (2002) | (3) A. Macho, et al.; Free Radic. Res. 37, 611 (2003) | (4) I. Sasahara, et al.; Biosci. Biotechnol. Biochem. 74, 274 (2010) | (5) X.J. Luo, et al.; Eur. J. Pharmacol. 650, 1 (2011) | (6) K. Shintaku, et al.; Br. J. Pharmacol. 165, 1476 (2012)
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