| Weight | 172.248 g/mol |
|---|---|
| Formula | C9H18NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
tempol (2226-96-2)
Score:
#381 in Biochemistry
,
#1338 in Biology
,
#1557 in Chemistry
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- Two-Week Administration of Tempol Attenuates Both Hypertension and Renal Excretion of 8-Iso Prostaglandin F2 (Hypertension, 1999)
- Tempol, a membrane-permeable radical scavenger, reduces oxidant stress-mediated renal dysfunction and injury in the rat (Kidney International, 2000)
- Chemistry and Antihypertensive Effects of Tempol and Other Nitroxides (Pharmacological Reviews, 2008)
- Effects of tempol and redox-cycling nitroxides in models of oxidative stress (Pharmacology & Therapeutics, 2010)
- Inhibition of oxygen-dependent radiation-induced damage by the nitroxide superoxide dismutase mimic, tempol (Archives of Biochemistry and Biophysics, 1991)
- Tempol, a Stable Free Radical, Is a Novel Murine Radiation Protector (Cancer Research, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1(CC(CC(N1[O])(C)C)O)C
-
InChIKeyUZFMOKQJFYMBGY-UHFFFAOYSA-N
- Pubchem - tempol
- Wikipedia - tempol
4-Hydroxy-TEMPO or TEMPOL, formally 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl, is a heterocyclic compound. Like the related TEMPO, it is used as a catalyst and chemical oxidant by virtue of being a stable radical. Its major appeal over TEMPO is that is less expensive, being produced from triacetone amine, which is itself made via the condensation of acetone and ammonia.
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