Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1993 1
1995 1
1999 1
2000 1
2012 1
2018 1
2019 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

8 results

Results by year

Filters applied: . Clear all
Page 1
Photoelectron spectroscopy of 1-nitropropane and 1-nitrobutane anions.
Adams CL, Knurr BJ, Weber JM. Adams CL, et al. J Chem Phys. 2012 Feb 14;136(6):064307. doi: 10.1063/1.3683250. J Chem Phys. 2012. PMID: 22360187
We present low-energy velocity map photoelectron imaging results for bare and Ar-solvated 1-nitropropane and 1-nitrobutane anions. We report the adiabatic electron affinity of 1-nitropropane as (223 6) meV and that of 1-nitrobutane as (240 6 meV). ...
We present low-energy velocity map photoelectron imaging results for bare and Ar-solvated 1-nitropropane and 1-nitrobutane ani …
Secondary nitroalkanes: induction of DNA repair in rat hepatocytes, activation by aryl sulfotransferase and hepatocarcinogenicity of 2-nitrobutane and 3-nitropentane in male F344 rats.
Fiala ES, Sodum RS, Hussain NS, Rivenson A, Dolan L. Fiala ES, et al. Toxicology. 1995 May 5;99(1-2):89-97. doi: 10.1016/0300-483x(94)03004-l. Toxicology. 1995. PMID: 7762004
The secondary nitroalkanes, 2-nitropropane, 2-nitrobutane, 3-nitropentane, 2-nitroheptane, nitrocyclopentane and nitrocyclohexane, as well as the primary nitroalkanes, 1-nitropropane, 1-nitrobutane, 1-nitropentane and 1-nitroheptane, were examined for their ability …
The secondary nitroalkanes, 2-nitropropane, 2-nitrobutane, 3-nitropentane, 2-nitroheptane, nitrocyclopentane and nitrocyclohexane, as well a …
Vibrational Autodetachment from Anionic Nitroalkane Chains: From Molecular Signatures to Thermionic Emission.
Adams CL, Hansen K, Weber JM. Adams CL, et al. J Phys Chem A. 2019 Oct 10;123(40):8562-8570. doi: 10.1021/acs.jpca.9b07780. Epub 2019 Sep 26. J Phys Chem A. 2019. PMID: 31532673
We report the kinetic energy distributions in electron autodetachment from nitroethane, 1-nitropropane, and 1-nitrobutane anions upon laser excitation of CH stretching modes measured using velocity map electron imaging. ...
We report the kinetic energy distributions in electron autodetachment from nitroethane, 1-nitropropane, and 1-nitrobutane anio …
Evaluation of secondary nitroalkanes, their nitronates, primary nitroalkanes, nitrocarbinols, and other aliphatic nitro compounds in the Ames Salmonella assay.
Conaway CC, Hussain NS, Way BM, Fiala ES. Conaway CC, et al. Mutat Res. 1991 Nov;261(3):197-207. doi: 10.1016/0165-1218(91)90068-w. Mutat Res. 1991. PMID: 1719412
The secondary nitroalkanes 2-nitropropane, 2-nitrobutane, 3-nitropentane and nitrocyclopentane, as well as their anionic forms (nitronates); the primary nitroalkanes 1-nitropropane, 1-nitrobutane, and 1-nitropentane and their respective nitronates; the nitrocarbinol …
The secondary nitroalkanes 2-nitropropane, 2-nitrobutane, 3-nitropentane and nitrocyclopentane, as well as their anionic forms (nitronates); …
Substrate specificity of a nitroalkane-oxidizing enzyme.
Gadda G, Fitzpatrick PF. Gadda G, et al. Arch Biochem Biophys. 1999 Mar 15;363(2):309-13. doi: 10.1006/abbi.1998.1081. Arch Biochem Biophys. 1999. PMID: 10068453
The V/K values for primary nitroalkanes increase with increasing length of the alkyl chain, reaching a maximum with 1-nitrobutane, suggesting a hydrophobic binding site sufficient to accommodate a four carbon chain. ...
The V/K values for primary nitroalkanes increase with increasing length of the alkyl chain, reaching a maximum with 1-nitrobutane …
Isovaleronitrile co-induced with its precursor, l-leucine, by herbivory in the common evening primrose stimulates foraging behavior of the predatory blue shield bug.
Noge K, Tamogami S. Noge K, et al. Biosci Biotechnol Biochem. 2018 Mar;82(3):395-406. doi: 10.1080/09168451.2018.1433019. Biosci Biotechnol Biochem. 2018. PMID: 29488452
In this study, l-leucine-derived nitrogen-containing compounds [isovaleronitrile (3-methylbutanenitrile), (E/Z)-isovaleraldoxime and 3-methyl-1-nitrobutane] and some terpenes were identified as a characteristic volatile blend from herbivore-infested O. biennis leave …
In this study, l-leucine-derived nitrogen-containing compounds [isovaleronitrile (3-methylbutanenitrile), (E/Z)-isovaleraldoxime and 3-methy …
Use of pH and kinetic isotope effects to dissect the effects of substrate size on binding and catalysis by nitroalkane oxidase.
Gadda G, Choe DY, Fitzpatrick PF. Gadda G, et al. Arch Biochem Biophys. 2000 Oct 1;382(1):138-44. doi: 10.1006/abbi.2000.2009. Arch Biochem Biophys. 2000. PMID: 11051107
The V/K values for primary nitroalkanes increase with increasing chain length, reaching a maximum with 1-nitrobutane [Gadda, G., and Fitzpatrick, P. F. (1999) Arch. Biochem. ...
The V/K values for primary nitroalkanes increase with increasing chain length, reaching a maximum with 1-nitrobutane [Gadda, G …
Metabolic activation of n-butyraldoxime by rat liver microsomal cytochrome P450. A requirement for the inhibition of aldehyde dehydrogenase.
DeMaster EG, Redfern B, Shirota FN, Crankshaw DL, Nagasawa HT. DeMaster EG, et al. Biochem Pharmacol. 1993 Jul 6;46(1):117-23. doi: 10.1016/0006-2952(93)90355-z. Biochem Pharmacol. 1993. PMID: 8347123
Hydroxylamine, postulated by others to be a metabolite of n-BO, inhibited AIDH via a catalase-mediated reaction and not through an NADPH-supported microsome-catalyzed reaction. Using GLC-mass spectrometry, 1-nitrobutane (an N-oxidation product) and butyronitrile (a …
Hydroxylamine, postulated by others to be a metabolite of n-BO, inhibited AIDH via a catalase-mediated reaction and not through an NADPH-sup …