6-IODONORDIHYDROCAPSAICIN

6-IODONORDIHYDROCAPSAICIN Basic information
Product Name:6-IODONORDIHYDROCAPSAICIN
Synonyms:6-IODONORDIHYDROCAPSAICIN;6'-Iodononivamide;6-IODONORDIHYDROCAPSAICIN USP/EP/BP;Nonanamide, N-[(4-hydroxy-2-iodo-5-methoxyphenyl)methyl]-
CAS:859171-97-4
MF:C17H26INO3
MW:419.3
EINECS:
Product Categories:Neurobiology;Pharmacologicals;Vanilloids;Vanilloid/TRPV channel
Mol File:859171-97-4.mol
6-IODONORDIHYDROCAPSAICIN Structure
6-IODONORDIHYDROCAPSAICIN Chemical Properties
Melting point 106-107 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
Boiling point 552.9±50.0 °C(Predicted)
density 1.375±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility H2O: insoluble
pka8.93±0.25(Predicted)
form solid
color white
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
MSDS Information
6-IODONORDIHYDROCAPSAICIN Usage And Synthesis
Uses6-?iodonordihydrocapsaicin (6-?I-?CPS) is a weak ERα agonist. It was demonstrated to induce luciferase gene expression.
DefinitionChEBI: N-[(4-hydroxy-2-iodo-5-methoxyphenyl)methyl]nonanamide is a member of phenols and a member of methoxybenzenes.
Biological Activitythe vanilloid trpv1 receptor, also known as vr1 receptor, belongs to the large family of ‘transient receptor potential’ (trp). trpv1 functions as a molecular integrator of nociceptive stimuli, including heat, protons and plant toxins, and is most abundant in peripheral sensory fibers of the c and ad type. 6-iodo-nordihydrocapsaicin is a potent trpv1 antagonist.
in vitrousing human recombinant trpv1, 6-iodonordihydrocapsaicin (ic50=10 nm against 100 nm capsaicin) was about four times more potent than the prototypical trpv1 antagonist, capsazepine [1].
in vivo6-iodonordihydrocapsaicin was tested against capsaicin also on native trpv1 in: (i) rat dorsal root ganglion neurons in culture; (ii) guinea-pig urinary bladder; and (iii) guinea-pig bronchi. in all cases, except for the guineapig bronchi, the compound was significantly more potent than capsazepine as a trpv1 antagonist [1].
IC 5010 nm against 100 nm capsaicin
references[1] appendino g, harrison s, de petrocellis l, daddario n, bianchi f, schiano moriello a, trevisani m, benvenuti f, geppetti p, di marzo v. halogenation of a capsaicin analogue leads to novel vanilloid trpv1 receptor antagonists. br j pharmacol. 2003 aug;139(8):1417-24.
6-IODONORDIHYDROCAPSAICIN Preparation Products And Raw materials
LIPOPHILIC SEPHADEX SEPHADEX G-75 SEPHADEX G-100 Dextran DEAE SEPHADEX

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