The store will not work correctly in the case when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
Biological Data Biological description Nitric oxide (NO) scavenging free radical. Reacts with NO stoichiometrically. Reduces withdrawal-induced anxiety behaviours.
Solubility & Handling Storage instructions +4°C
Solubility overview Soluble in water (100mg/ml) or DMSO
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data Chemical name 2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide potassium salt
Chemical structure
Molecular Formula C14 H16 KN2 O4
PubChem identifier 2733502
SMILES CC1(C([N+](=C(N1[O])C2=CC=C(C=C2)C(=O)[O-])[O-])(C)C)C.[K+]
InChiKey VYEUQMVIGXFZQU-UHFFFAOYSA-M
References for Carboxy-PTIO, potassium salt References are publications that support the biological activity of the product
Effects of nitric oxide synthase inhibition in the dorsolateral periaqueductal gray matter on ethanol withdrawal-induced anxiety-like behavior in rats. Bonassoli VT et al (2013) Psychopharmacology (Berl) 228(3) : 487-98. Nitric oxide scavenging causes remodeling of the endoplasmic reticulum, Golgi apparatus and mitochondria in pulmonary arterial endothelial cells. Lee JE et al (2013) Nitric Oxide 33 : 64-73. Vasodilator effect of carboxy-2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl in the coronary circulation: in vivo and in vitro studies. Tsunoda R et al (1994) Eur J Pharmacol 262(1-2) : 55-63. Antagonistic action of imidazolineoxyl N-oxides against endothelium-derived relaxing factor/.NO through a radical reaction. Akaike T et al (1993) Biochemistry 32(3) : 827-32.
Tell us about your publication! What Hello Bio product(s) have you cited?
Captcha Please type the letters and numbers below Submit