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Structural characteristics and harmonic vibrational analysis of the stable conformer of 2,3-epoxypropanol by quantum chemical methods.
Arjunan V, Rani T, Santhanam R, Mohan S. Arjunan V, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2012 Oct;96:24-34. doi: 10.1016/j.saa.2012.05.012. Epub 2012 May 12. Spectrochim Acta A Mol Biomol Spectrosc. 2012. PMID: 22652541
The FT-IR and FT-Raman spectra of H bond inner conformer of 2,3-epoxypropanol have been recorded in the regions 3700-400 and 3700-100 cm(-1), respectively. ...
The FT-IR and FT-Raman spectra of H bond inner conformer of 2,3-epoxypropanol have been recorded in the regions 3700-40 …
The metabolism of 3-chloro,- 3-bromo- and 3-iodoprpan-1,2-diol in rats and mice.
Jones AR. Jones AR. Xenobiotica. 1975 Mar;5(3):155-65. doi: 10.3109/00498257509056101. Xenobiotica. 1975. PMID: 1166663
When incubated with rat liver supernatant, the compounds do not conjugate with glutathione and their general chemical reactivity suggests that they react via a common intermediate proposed to be glycidol (2,3-epoxypropanol, IV). As the epoxide produces the sa …
When incubated with rat liver supernatant, the compounds do not conjugate with glutathione and their general chemical reactivity suggests th …
The active centre of rabbit muscle triose phosphate isomerase. The site that is labelled by glycidol phosphate.
Miller JC, Waley SG. Miller JC, et al. Biochem J. 1971 Jun;123(2):163-70. doi: 10.1042/bj1230163. Biochem J. 1971. PMID: 4942534 Free PMC article.
1. Glycidol (2,3-epoxypropanol) phosphate is a specific irreversible inhibitor of rabbit muscle triose phosphate isomerase (EC 5.3.1.1); the site of attachment has now been studied. 2. ...
1. Glycidol (2,3-epoxypropanol) phosphate is a specific irreversible inhibitor of rabbit muscle triose phosphate isomer …
Metabolism of inhaled dihalomethanes in vivo: differentiation of kinetic constants for two independent pathways.
Gargas ML, Clewell HJ 3rd, Andersen ME. Gargas ML, et al. Toxicol Appl Pharmacol. 1986 Feb;82(2):211-23. doi: 10.1016/0041-008x(86)90196-1. Toxicol Appl Pharmacol. 1986. PMID: 3945949
We also studied the effects of pyrazole (which inhibits microsomal oxidation) and 2,3-epoxypropanol (which depletes GSH) on dihalomethane metabolism. Pyrazole abolished CO production from CH2Br2, CH2BrCl, and CH2Cl2. ...
We also studied the effects of pyrazole (which inhibits microsomal oxidation) and 2,3-epoxypropanol (which depletes GSH …