H57009
3-Hydroxypyridine
98%
Synonym(s):
3-Pyridinol, 3-Pyridone
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About This Item
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Assay
98%
mp
125-128 °C (lit.)
SMILES string
Oc1cccnc1
InChI
1S/C5H5NO/c7-5-2-1-3-6-4-5/h1-4,7H
InChI key
GRFNBEZIAWKNCO-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Chemical research in toxicology, 16(2), 232-241 (2003-02-18)
2-hydroxyaldehydes have been previously identified as products of lipid peroxidation, and although they represent the simplest reducing sugars, their potential for modification of proteins under physiological conditions has not been investigated. Here, 2-hydroxyaldehydes were found to condense with amines in
European journal of medicinal chemistry, 39(8), 691-697 (2004-07-28)
Four trans-planaramineplatinum(II) complexes code named YH9, YH10, YH11 and YH12, each of the form trans-PtL(NH(3))Cl(2) where L = 2-hydroxypyridine and 3-hydroxypyridine, imidazole, and imidazo(1,2-alpha)pyridine for YH9, YH10, YH11 and YH12, respectively. All of the compounds have significant anticancer activity against
Bulletin of experimental biology and medicine, 148(4), 587-591 (2010-04-17)
Succinate-containing derivatives of 3-hydroxypyridine, mexidol and proxypin, serve as succinate donors for the respiratory chain and contribute to activation of the succinate oxidase pathway of oxidation. Under conditions of hypoxia, these changes promote recovery of aerobic energy production, normalization of
The Journal of organic chemistry, 68(7), 2874-2881 (2003-03-29)
The tautomeric equilibria of a series of 3-hydroxypyridine derivatives including pyridoxal-5'-phosphate (PLP), the active form of vitamin B(6), have been studied using density functional calculations (B3LYP/6-311+G//B3LYP/6-31G) in the gas phase and in different solvents. Three different approaches, namely continuum, discrete
Journal of the American Chemical Society, 130(32), 10793-10801 (2008-07-23)
Subdomain IIA binding site of human serum albumin (HSA) was characterized by examining the change in HSA fluorescence in the native, unfolded, and refolded states. The study was carried out in the absence and presence of small molecular probes using
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